PSMA Targeting Trispecific Proteins and Methods of Use

Abstract

Provided herein are prostate specific membrane antigen (PSMA) targeting trispecific proteins comprising a domain binding to CD3, a half-life extension domain, and a domain binding to PSMA. Also provided are pharmaceutical compositions thereof, as well as nucleic acids, recombinant expression vectors and host cells for making such PSMA targeting trispecific proteins. Also disclosed are methods of using the disclosed PSMA targeting trispecific proteins in the prevention, and/or treatment diseases, conditions and disorders.

Description

CROSS-REFERENCE

[0001] This application is a continuation application of U.S. patent application Ser. No. 15/821,530, filed on Nov. 22, 2017, and claims the benefit of U.S. Provisional Application Nos. 62/426,069 filed Nov. 23, 2016, and 62/426,077 filed Nov. 23, 2016, which are incorporated by reference herein in their entirety.

SEQUENCE LISTING

[0002] The instant application contains a Sequence Listing which has been submitted electronically in ASCII format and is hereby incorporated by reference in its entirety. Said ASCII copy, created on Nov. 22, 2017, is named 47517-708_201_SL.txt and is 150,911 bytes in size.

BACKGROUND OF THE INVENTION

[0003] The selective destruction of an individual cell or a specific cell type is often desirable in a variety of clinical settings. For example, it is a primary goal of cancer therapy to specifically destroy tumor cells, while leaving healthy cells and tissues intact and undamaged. One such method is by inducing an immune response against the tumor, to make immune effector cells such as natural killer (NK) cells or cytotoxic T lymphocytes (CTLs) attack and destroy tumor cells.

SUMMARY OF THE INVENTION

[0004] Provided herein are trispecific antigen-binding protein, pharmaceutical compositions thereof, as nucleic acids, recombinant expression vectors and host cells for making such trispecific antigen-binding proteins, and methods of use for the treatment of diseases, disorders, or conditions. In one aspect, described herein are prostate specific membrane antigen (PSMA) targeting trispecific proteins, wherein said proteins comprise (a) a first domain (A) which specifically binds to human CD3; (b) a second domain (B) which is a half-life extension domain; and (c) a third domain (C) which specifically binds to PSMA, wherein the domains are linked in the order H2N-(A)-(C)-(B)-COOH, H2N-(B)-(A)-(C)-COOH, H2N-(C)-(B)-(A)-COOH, or by linkers L1 and L2. In some embodiments, the first domain comprises a variable light chain and variable heavy chain each of which is capable of specifically binding to human CD3. In some embodiments, the first domain comprises one or more sequences selected from the group consisting of SEQ ID NO: 1-88. In some embodiments, the first domain is humanized or human. In some embodiments, the first domain has a KD binding of 150 nM or less to CD3 on CD3 expressing cells. In some embodiments, the second domain binds human serum albumin. In some embodiments, the second domain comprises a scFv, a variable heavy domain (VH), a variable light domain (VL), a peptide, a ligand, or a small molecule. In some embodiments, the second domain comprises one or more sequences selected from the group consisting of SEQ ID NOs: 89-112. In some embodiments, the third domain comprises a scFv, a VH domain, a VL domain, a non-Ig domain, a ligand, a knottin, or a small molecule entity that specifically binds to PSMA. In some embodiments, the third domain comprises one or more sequences selected from the group consisting of SEQ ID NOs: 113-140.

[0005] In some embodiments, linkers L1 and L2 are each independently selected from (GS)n (SEQ ID NO: 153), (GGS)n (SEQ ID NO: 154), (GGGS)n (SEQ ID NO: 155), (GGSG)n (SEQ ID NO: 156), (GGSGG)n (SEQ ID NO: 157), or (GGGGS)n (SEQ ID NO: 158), wherein n is 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10. In some embodiments, linkers L1 and L2 are each independently (GGGGS)4 (SEQ ID NO: 159) or (GGGGS)3 (SEQ ID NO: 160). In some embodiments, the domains are linked in the order H2N-(A)-(C)-(B)-COOH. In some embodiments, the domains are linked in the order H2N-(B)-(C)-(A)-COOH.

[0006] In some embodiments, the protein is less than about 80 kDa. In some embodiments, the protein is about 50 to about 75 kDa. In some embodiments, the protein is less than about 60 kDa. In some embodiments, the protein has an elimination half-time of at least about 50 hours. In some embodiments, the protein has an elimination half-time of at least about 100 hours. In some embodiments, the protein has increased tissue penetration as compared to an IgG to the same PSMA.

[0007] In some embodiments, the protein comprises a sequence selected from the group consisting of SEQ ID NO: 140-152.

[0008] In another aspect, provided herein are pharmaceutical composition comprising (i) the PSMA targeting trispecific protein according to any one of the above embodiments and (ii) a pharmaceutically acceptable carrier.

[0009] Also provided herein are methods of treating an individual in need of treatment of cancer, the method comprising administration of an effective amount of the pharmaceutical composition or PSMA targeting trispecific proteins according to any of the above embodiments. In some embodiments, the cancer is prostate cancer or renal cancer.

[0010] One embodiment provides a PSMA targeting trispecific protein, wherein said protein comprises (a) a first domain (A) which specifically binds to human CD3; (b) a second domain (B) which is a half-life extension domain; and (c) a third domain (C) which specifically binds to PSMA, wherein the second domain comprises one or more sequences selected from the group consisting of SEQ ID NOs: 113-140. In some embodiments, domains are linked in the order H.sub.2N-(A)-(C)-(B)-COOH, H.sub.2N-(B)-(A)-(C)-COOH, H.sub.2N-(C)-(B)-(A)-COOH, or by linkers L1 and L2. In some embodiments, the first domain comprises one or more sequences selected from the group consisting of SEQ ID NO: 1-88. In some embodiments, the second domain comprises one or more sequences selected from the group consisting of SEQ ID NO: 89-112.

[0011] One embodiment provides a PSMA targeting trispecific protein, wherein said protein comprises a sequence selected from the group consisting of SEQ ID NO: 140-152. In some embodiments, said protein comprises a sequence selected from the group consisting of SEQ ID NO: 150-152.

[0012] One embodiment provides a prostate specific membrane antigen (PSMA) targeting trispecific protein, wherein said protein comprises (a) a first domain (A) which specifically binds to human CD3; (b) a second domain (B) which is a half-life extension domain; and (c) a third domain (C) which specifically binds to PSMA, wherein the domains are linked in the order H.sub.2N-(C)-(B)-(A)-COOH, or by linkers L1 and L2, and wherein the third domain comprises one or more sequences selected from the group consisting of SEQ ID NO: 113-140.

[0013] One embodiment provides a PSMA targeting trispecific protein, wherein said protein comprises (a) a first domain (A) which specifically binds to human CD3; (b) a second domain (B) which is a half-life extension domain; and (c) a third domain (C) which specifically binds to PSMA, wherein the domains are linked in the order H.sub.2N-(C)-(B)-(A)-COOH, or by linkers L1 and L2, and wherein the first domain comprises one or more sequences selected from the group consisting of SEQ ID NO: 1-88.

[0014] One embodiment provides a method of treating prostate cancer, the method comprising administration of an effective amount of a PSMA targeting trispecific protein, wherein said protein comprises (a) a first domain (A) which specifically binds to human CD3; (b) a second domain (B) which is a half-life extension domain; and (c) a third domain (C) which specifically binds to PSMA, wherein the domains are linked in the order H.sub.2N-(C)-(B)-(A)-COOH, or by linkers L1 and L2, and wherein the third domain comprises one or more sequences selected from the group consisting of SEQ ID NO: 113-140.

[0015] One embodiment provides a method of treating prostate cancer, the method comprising administration of an effective amount of a PSMA targeting trispecific protein, wherein said protein comprises (a) a first domain (A) which specifically binds to human CD3; (b) a second domain (B) which is a half-life extension domain; and (c) a third domain (C) which specifically binds to PSMA, wherein the domains are linked in the order H.sub.2N-(C)-(B)-(A)-COOH, or by linkers L1 and L2, and wherein the first domain comprises one or more sequences selected from the group consisting of SEQ ID NO: 1-88.

INCORPORATION BY REFERENCE

[0016] All publications, patents, and patent applications mentioned in this specification are herein incorporated by reference to the same extent as if each individual publication, patent, or patent application was specifically and individually indicated to be incorporated by reference.

BRIEF DESCRIPTION OF THE DRAWINGS

[0017] The novel features of the invention are set forth with particularity in the appended claims. A better understanding of the features and advantages of the present invention will be obtained by reference to the following detailed description that sets forth illustrative embodiments, in which the principles of the invention are utilized, and the accompanying drawings of which:

[0018] FIG. 1 is schematic representation of an exemplary PMSA targeting trispecific antigen-binding protein where the protein has an constant core element comprising an anti-CDR3.epsilon. single chain variable fragment (scFv) and an anti-HSA variable heavy chain region; and a PMSA binding domain that can be a VH, scFv, a non-Ig binder, or ligand.

[0019] FIGS. 2A-B compare the ability of exemplary PSMA targeting trispecific proteins (PSMA targeting TriTAC molecules) with different affinities for CD3 to induce T cells to kill human prostate cancer cells. FIG. 2A shows killing by different PMSA targeting TriTAC molecules in prostate cancer model LNCaP. FIG. 2B shows killing by different PMSA targeting TriTAC molecules in prostate cancer model 22Rv1. FIG. 2C shows EC50 values for PMSA targeting TriTAC in LNCaP and 22Rv1 prostate cancer models.

[0020] FIG. 3 shows the serum concentration of PSMA targeting TriTAC C236 in Cynomolgus monkeys after i.v. administration (100 .mu.g/kg) over three weeks.

[0021] FIG. 4 shows the serum concentration of PSMA targeting TriTAC molecules with different CD3 affinities in Cynomolgus monkeys after i.v. administration (100 .mu.g/kg) over three weeks.

[0022] FIGS. 5A-C show the ability of PSMA targeting TriTAC molecules with different affinities for PSMA to induce T cells to kill the human prostate cancer cell line LNCaP. FIG. 5A shows the experiment performed in the absence of human serum albumin with a PSMA targeting BiTE as positive control. FIG. 5B shows the experiment performed in the presence of human serum albumin with a PSMA targeting BiTE as positive control. FIG. 5C shows EC50 values for PMSA targeting TriTAC in the presence or absence of HSA with a PSMA targeting BiTE as a positive control in LNCaP prostate cancer models.

[0023] FIG. 6 demonstrates the ability of PSMA targeting TriTAC molecules to inhibit tumor growth of human prostate cancer cells in a mouse xenograft experiment.

[0024] FIGS. 7A-D illustrates the specificity of TriTAC molecules in cell killing assays with target cell lines that do or do not express the target protein. FIG. 7A shows EGFR and PSMA expression in LNCaP, KMS12BM, and OVCAR8 cell lines. FIG. 7B shows killing of LNCaP tumor cells by PSMA, EGFR, and negative control TriTACs. FIG. 7C shows killing of KMS12BM tumor cells by PSMA, EGFR, and negative control TriTACs. FIG. 7D shows killing of OVCAR8 cells by PSMA, EGFR, and negative control TriTACs.

[0025] FIGS. 8A-D depict the impact of pre-incubation at 37.degree. C. and freeze/thaw cycles on TriTAC activity. FIG. 8A shows PSMA TriTAC C235 activity after pre-incubation at 37.degree. C. or freeze/thaw cycles. FIG. 8B shows PSMA TriTAC C359 activity after pre-incubation at 37.degree. C. or freeze/thaw cycles. FIG. 8C shows PSMA TriTAC C360 activity after pre-incubation at 37.degree. C. or freeze/thaw cycles. FIG. 8D shows PSMA TriTAC C361 activity after pre-incubation at 37.degree. C. or freeze/thaw cycles.

[0026] FIGS. 9A-B depict the activity of a PSMA targeting TriTAC molecule of this disclosure in redirected T cell killing in T cell dependent cellular cytotoxicity assays (TDCC). FIG. 9A shows the impact of the PSMA targeting TriTAC molecule in redirecting cynomolgus peripheral blood mononuclear cells (PBMCs), from cynomolgus monkey donor G322, in killing LNCaP cells. FIG. 9B shows the impact of the PSMA targeting TriTAC molecule in redirecting cynomolgus PBMCs, from cynomolgus monkey donor D173, to kill MDAPCa2b cells.

[0027] FIG. 10 depicts the impact of a PSMA targeting TriTAC molecule of this disclosure on expression of T cell activation markers CD25 and CD69.

[0028] FIG. 11 depicts the ability of a PSMA targeting TriTAC molecule of this disclosure to stimulate T cell proliferation in the presence of PSMA expressing target cells.

[0029] FIGS. 12A-B depict redirected T cell killing of LnCaP cells by PSMA targeting TriTAC molecules. FIG. 12A shows redirected T cell killing of LnCaP cells by PSMA PH1T TriTAC (SEQ ID No: 150) and PSMA PH1 TriTAC (SEQ ID NO: 151) molecules. FIG. 12B shows redirected T cell killing of LnCaP cells by PSMA Z2 TriTAC (SEQ ID NO: 152).

DETAILED DESCRIPTION OF THE INVENTION

[0030] Described herein are trispecific proteins that target prostate specific membrane antigen (PSMA), pharmaceutical compositions thereof, as well as nucleic acids, recombinant expression vectors and host cells for making such proteins thereof. Also provided are methods of using the disclosed PSMA targeting trispecific proteins in the prevention, and/or treatment of diseases, conditions and disorders. The PSMA targeting trispecific proteins are capable of specifically binding to PSMA as well as CD3 and have a half-life extension domain, such as a domain binding to human serum albumin (HSA). FIG. 1 depicts one non-limiting example of a trispecific antigen-binding protein.

[0031] In one aspect, the PSMA targeting trispecific proteins comprise a domain (A) which specifically binds to CD3, a domain (B) which specifically binds to human serum albumin (HSA), and a domain (C) which specifically binds to PSMA. The three domains in PSMA targeting trispecific proteins are arranged in any order. Thus, it is contemplated that the domain order of the PSMA targeting trispecific proteins are:

[0032] H.sub.2N-(A)-(B)-(C)-COOH,

[0033] H.sub.2N-(A)-(C)-(B)-COOH,

[0034] H.sub.2N-(B)-(A)-(C)-COOH,

[0035] H.sub.2N-(B)-(C)-(A)-COOH,

[0036] H.sub.2N-(C)-(B)-(A)-COOH, or

[0037] H.sub.2N-(C)-(A)-(B)-COOH.

[0038] In some embodiments, the PSMA targeting trispecific proteins have a domain order of H.sub.2N-(A)-(B)-(C)-COOH. In some embodiments, the PSMA targeting trispecific proteins have a domain order of H.sub.2N-(A)-(C)-(B)-COOH. In some embodiments, the PSMA targeting trispecific proteins have a domain order of H.sub.2N-(B)-(A)-(C)-COOH. In some embodiments, the PSMA targeting trispecific proteins have a domain order of H.sub.2N-(B)-(C)-(A)-COOH. In some embodiments, the PSMA targeting trispecific proteins have a domain order of H.sub.2N-(C)-(B)-(A)-COOH. In some embodiments, the PSMA targeting trispecific proteins have a domain order of H.sub.2N-(C)-(A)-(B)-COOH.

[0039] In some embodiments, the PSMA targeting trispecific proteins have the HSA binding domain as the middle domain, such that the domain order is H.sub.2N-(A)-(B)-(C)-COOH or H.sub.2N-(C)-(B)-(A)-COOH. It is contemplated that in such embodiments where the HSA binding domain as the middle domain, the CD3 and PSMA binding domains are afforded additional flexibility to bind to their respective targets.

[0040] In some embodiments, the PSMA targeting trispecific proteins described herein comprise a polypeptide having a sequence described in Table 10 (SEQ ID NO: 140-152) and subsequences thereof. In some embodiments, the trispecific antigen binding protein comprises a polypeptide having at least 70%-95% or more homology to a sequence described in Table 10 (SEQ ID NO: 140-152). In some embodiments, the trispecific antigen binding protein comprises a polypeptide having at least 70%, 75%, 80%, 85%, 90%, 95%, or more homology to a sequence described in Table 10 (SEQ ID NO: 140-152). In some embodiments, the trispecific antigen binding protein has a sequence comprising at least a portion of a sequence described in Table 10 (SEQ ID NO: 140-152). In some embodiments, the PSMA trispecific antigen-binding protein comprises a polypeptide comprising one or more of the sequences described in Table 10 (SEQ ID NO: 140-152). In further embodiments, the PSMA trispecific antigen-binding protein comprises one or more CDRs as described in the sequences in Table 10 (SEQ ID NO: 140-152).

[0041] The PSMA targeting trispecific proteins described herein are designed to allow specific targeting of cells expressing PSMA by recruiting cytotoxic T cells. This improves efficacy compared to ADCC (antibody dependent cell-mediated cytotoxicity), which is using full length antibodies directed to a sole antigen and is not capable of directly recruiting cytotoxic T cells. In contrast, by engaging CD3 molecules expressed specifically on these cells, the PSMA targeting trispecific proteins can crosslink cytotoxic T cells with cells expressing PSMA in a highly specific fashion, thereby directing the cytotoxic potential of the T cell towards the target cell. The PSMA targeting trispecific proteins described herein engage cytotoxic T cells via binding to the surface-expressed CD3 proteins, which form part of the TCR. Simultaneous binding of several PSMA trispecific antigen-binding protein to CD3 and to PSMA expressed on the surface of particular cells causes T cell activation and mediates the subsequent lysis of the particular PSMA expressing cell. Thus, PSMA targeting trispecific proteins are contemplated to display strong, specific and efficient target cell killing. In some embodiments, the PSMA targeting trispecific proteins described herein stimulate target cell killing by cytotoxic T cells to eliminate pathogenic cells (e.g., tumor cells expressing PSMA). In some of such embodiments, cells are eliminated selectively, thereby reducing the potential for toxic side effects.

[0042] The PSMA targeting trispecific proteins described herein confer further therapeutic advantages over traditional monoclonal antibodies and other smaller bispecific molecules. Generally, the effectiveness of recombinant protein pharmaceuticals depends heavily on the intrinsic pharmacokinetics of the protein itself. One such benefit here is that the PSMA targeting trispecific proteins described herein have extended pharmacokinetic elimination half-time due to having a half-life extension domain such as a domain specific to HSA. In this respect, the PSMA targeting trispecific proteins described herein have an extended serum elimination half-time of about two, three, about five, about seven, about 10, about 12, or about 14 days in some embodiments. This contrasts to other binding proteins such as BiTE or DART molecules which have relatively much shorter elimination half-times. For example, the BiTE CD19.times.CD3 bispecific scFv-scFv fusion molecule requires continuous intravenous infusion (i.v.) drug delivery due to its short elimination half-time. The longer intrinsic half-times of the PSMA targeting trispecific proteins solve this issue thereby allowing for increased therapeutic potential such as low-dose pharmaceutical formulations, decreased periodic administration and/or novel pharmaceutical compositions.

[0043] The PSMA targeting trispecific proteins described herein also have an optimal size for enhanced tissue penetration and tissue distribution. Larger sizes limit or prevent penetration or distribution of the protein in the target tissues. The PSMA targeting trispecific proteins described herein avoid this by having a small size that allows enhanced tissue penetration and distribution. Accordingly, the PSMA targeting trispecific proteins described herein, in some embodiments have a size of about 50 kD to about 80 kD, about 50 kD to about 75 kD, about 50 kD to about 70 kD, or about 50 kD to about 65 kD. Thus, the size of the PSMA targeting trispecific proteins is advantageous over IgG antibodies which are about 150 kD and the BiTE and DART diabody molecules which are about 55 kD but are not half-life extended and therefore cleared quickly through the kidney.

[0044] In further embodiments, the PSMA targeting trispecific proteins described herein have an optimal size for enhanced tissue penetration and distribution. In these embodiments, the PSMA targeting trispecific proteins are constructed to be as small as possible, while retaining specificity toward its targets. Accordingly, in these embodiments, the PSMA targeting trispecific proteins described herein have a size of about 20 kD to about 40 kD or about 25 kD to about 35 kD to about 40 kD, to about 45 kD, to about 50 kD, to about 55 kD, to about 60 kD, to about 65 kD. In some embodiments, the PSMA targeting trispecific proteins described herein have a size of about 50 kD, 49, kD, 48 kD, 47 kD, 46 kD, 45 kD, 44 kD, 43 kD, 42 kD, 41 kD, 40 kD, about 39 kD, about 38 kD, about 37 kD, about 36 kD, about 35 kD, about 34 kD, about 33 kD, about 32 kD, about 31 kD, about 30 kD, about 29 kD, about 28 kD, about 27 kD, about 26 kD, about 25 kD, about 24 kD, about 23 kD, about 22 kD, about 21 kD, or about 20 kD. An exemplary approach to the small size is through the use of single domain antibody (sdAb) fragments for each of the domains. For example, a particular PSMA trispecific antigen-binding protein has an anti-CD3 sdAb, anti-HSA sdAb and an sdAb for PSMA. This reduces the size of the exemplary PSMA trispecific antigen-binding protein to under 40 kD. Thus in some embodiments, the domains of the PSMA targeting trispecific proteins are all single domain antibody (sdAb) fragments. In other embodiments, the PSMA targeting trispecific proteins described herein comprise small molecule entity (SME) binders for HSA and/or the PSMA. SME binders are small molecules averaging about 500 to 2000 Da in size and are attached to the PSMA targeting trispecific proteins by known methods, such as sortase ligation or conjugation. In these instances, one of the domains of PSMA trispecific antigen-binding protein is a sortase recognition sequence, e.g., LPETG (SEQ ID NO: 57). To attach a SME binder to PSMA trispecific antigen-binding protein with a sortase recognition sequence, the protein is incubated with a sortase and a SME binder whereby the sortase attaches the SME binder to the recognition sequence. Known SME binders include MIP-1072 and MIP-1095 which bind to prostate-specific membrane antigen (PSMA). In yet other embodiments, the domain which binds to PSMA of PSMA targeting trispecific proteins described herein comprise a knottin peptide for binding PSMA. Knottins are disulfide-stabilized peptides with a cysteine knot scaffold and have average sizes about 3.5 kD. Knottins have been contemplated for binding to certain tumor molecules such as PSMA. In further embodiments, domain which binds to PSMA of PSMA targeting trispecific proteins described herein comprise a natural PSMA ligand.

[0045] Another feature of the PSMA targeting trispecific proteins described herein is that they are of a single-polypeptide design with flexible linkage of their domains. This allows for facile production and manufacturing of the PSMA targeting trispecific proteins as they can be encoded by single cDNA molecule to be easily incorporated into a vector. Further, because the PSMA targeting trispecific proteins described herein are a monomeric single polypeptide chain, there are no chain pairing issues or a requirement for dimerization. It is contemplated that the PSMA targeting trispecific proteins described herein have a reduced tendency to aggregate unlike other reported molecules such as bispecific proteins with Fc-gamma immunoglobulin domains.

[0046] In the PSMA targeting trispecific proteins described herein, the domains are linked by internal linkers L1 and L2, where L1 links the first and second domain of the PSMA targeting trispecific proteins and L2 links the second and third domains of the PSMA targeting trispecific proteins. Linkers L1 and L2 have an optimized length and/or amino acid composition. In some embodiments, linkers L1 and L2 are the same length and amino acid composition. In other embodiments, L1 and L2 are different. In certain embodiments, internal linkers L1 and/or L2 are "short", i.e., consist of 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12 amino acid residues. Thus, in certain instances, the internal linkers consist of about 12 or less amino acid residues. In the case of 0 amino acid residues, the internal linker is a peptide bond. In certain embodiments, internal linkers L1 and/or L2 are "long", i.e., consist of 15, 20 or 25 amino acid residues. In some embodiments, these internal linkers consist of about 3 to about 15, for example 8, 9 or 10 contiguous amino acid residues. Regarding the amino acid composition of the internal linkers L1 and L2, peptides are selected with properties that confer flexibility to the PSMA targeting trispecific proteins, do not interfere with the binding domains as well as resist cleavage from proteases. For example, glycine and serine residues generally provide protease resistance. Examples of internal linkers suitable for linking the domains in the PSMA targeting trispecific proteins include but are not limited to (GS)n (SEQ ID NO: 153), (GGS).sub.n (SEQ ID NO: 154), (GGGS).sub.n (SEQ ID NO: 155), (GGSG).sub.n (SEQ ID NO: 156), (GGSGG).sub.n (SEQ ID NO: 157), or (GGGGS).sub.n (SEQ ID NO: 158), wherein n is 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10. In one embodiment, internal linker L1 and/or L2 is (GGGGS).sub.4 (SEQ ID NO: 159) or (GGGGS).sub.3 (SEQ ID NO: 160).

CD3 Binding Domain

[0047] The specificity of the response of T cells is mediated by the recognition of antigen (displayed in context of a major histocompatibility complex, MEW) by the TCR. As part of the TCR, CD3 is a protein complex that includes a CD3.gamma. (gamma) chain, a CD3.delta. (delta) chain, and two CD3.epsilon. (epsilon) chains which are present on the cell surface. CD3 associates with the .alpha. (alpha) and .beta. (beta) chains of the TCR as well as CD3.zeta. (zeta) altogether to comprise the complete TCR. Clustering of CD3 on T cells, such as by immobilized anti-CD3 antibodies leads to T cell activation similar to the engagement of the T cell receptor but independent of its clone-typical specificity.

[0048] In one aspect, the PSMA targeting trispecific proteins described herein comprise a domain which specifically binds to CD3. In one aspect, the PSMA targeting trispecific proteins described herein comprise a domain which specifically binds to human CD3. In some embodiments, the PSMA targeting trispecific proteins described herein comprise a domain which specifically binds to CD3.gamma.. In some embodiments, the PSMA targeting trispecific proteins described herein comprise a domain which specifically binds to CD3.delta.. In some embodiments, the PSMA targeting trispecific proteins described herein comprise a domain which specifically binds to CD3.epsilon..

[0049] In further embodiments, the PSMA targeting trispecific proteins described herein comprise a domain which specifically binds to the TCR. In certain instances, the PSMA targeting trispecific proteins described herein comprise a domain which specifically binds the a chain of the TCR. In certain instances, the PSMA targeting trispecific proteins described herein comprise a domain which specifically binds the .beta. chain of the TCR.

[0050] In certain embodiments, the CD3 binding domain of the PSMA targeting trispecific proteins described herein exhibit not only potent CD3 binding affinities with human CD3, but show also excellent crossreactivity with the respective cynomolgus monkey CD3 proteins. In some instances, the CD3 binding domain of the PSMA targeting trispecific proteins are cross-reactive with CD3 from cynomolgus monkey. In certain instances, human:cynomolgous K.sub.D ratios for CD3 are between 5 and 0.2.

[0051] In some embodiments, the CD3 binding domain of the PSMA trispecific antigen-binding protein can be any domain that binds to CD3 including but not limited to domains from a monoclonal antibody, a polyclonal antibody, a recombinant antibody, a human antibody, a humanized antibody. In some instances, it is beneficial for the CD3 binding domain to be derived from the same species in which the PSMA trispecific antigen-binding protein will ultimately be used in. For example, for use in humans, it may be beneficial for the CD3 binding domain of the PSMA trispecific antigen-binding protein to comprise human or humanized residues from the antigen binding domain of an antibody or antibody fragment.

[0052] Thus, in one aspect, the antigen-binding domain comprises a humanized or human antibody or an antibody fragment, or a murine antibody or antibody fragment. In one embodiment, the humanized or human anti-CD3 binding domain comprises one or more (e.g., all three) light chain complementary determining region 1 (LC CDR1), light chain complementary determining region 2 (LC CDR2), and light chain complementary determining region 3 (LC CDR3) of a humanized or human anti-CD3 binding domain described herein, and/or one or more (e.g., all three) heavy chain complementary determining region 1 (HC CDR1), heavy chain complementary determining region 2 (HC CDR2), and heavy chain complementary determining region 3 (HC CDR3) of a humanized or human anti-CD3 binding domain described herein, e.g., a humanized or human anti-CD3 binding domain comprising one or more, e.g., all three, LC CDRs and one or more, e.g., all three, HC CDRs.

[0053] In some embodiments, the humanized or human anti-CD3 binding domain comprises a humanized or human light chain variable region specific to CD3 where the light chain variable region specific to CD3 comprises human or non-human light chain CDRs in a human light chain framework region. In certain instances, the light chain framework region is a .lamda. (lamda) light chain framework. In other instances, the light chain framework region is a .kappa. (kappa) light chain framework.

[0054] In some embodiments, the humanized or human anti-CD3 binding domain comprises a humanized or human heavy chain variable region specific to CD3 where the heavy chain variable region specific to CD3 comprises human or non-human heavy chain CDRs in a human heavy chain framework region.

[0055] In certain instances, the complementary determining regions of the heavy chain and/or the light chain are derived from known anti-CD3 antibodies, such as, for example, muromonab-CD3 (OKT3), otelixizumab (TRX4), teplizumab (MGA031), visilizumab (Nuvion), SP34, TR-66 or X35-3, VIT3, BMA030 (BW264/56), CLB-T3/3, CRIS7, YTH12.5, F111-409, CLB-T3.4.2, TR-66, WT32, SPv-T3b, 11D8, XIII-141, XIII-46, XIII-87, 12F6, T3/RW2-8C8, T3/RW2-4B6, OKT3D, M-T301, SMC2, F101.01, UCHT-1 and WT-31.

[0056] In one embodiment, the anti-CD3 binding domain is a single chain variable fragment (scFv) comprising a light chain and a heavy chain of an amino acid sequence provided herein. As used herein, "single chain variable fragment" or "scFv" refers to an antibody fragment comprising a variable region of a light chain and at least one antibody fragment comprising a variable region of a heavy chain, wherein the light and heavy chain variable regions are contiguously linked via a short flexible polypeptide linker, and capable of being expressed as a single polypeptide chain, and wherein the scFv retains the specificity of the intact antibody from which it is derived. In an embodiment, the anti-CD3 binding domain comprises: a light chain variable region comprising an amino acid sequence having at least one, two or three modifications (e.g., substitutions) but not more than 30, 20 or 10 modifications (e.g., substitutions) of an amino acid sequence of a light chain variable region provided herein, or a sequence with 95-99% identity with an amino acid sequence provided herein; and/or a heavy chain variable region comprising an amino acid sequence having at least one, two or three modifications (e.g., substitutions) but not more than 30, 20 or 10 modifications (e.g., substitutions) of an amino acid sequence of a heavy chain variable region provided herein, or a sequence with 95-99% identity to an amino acid sequence provided herein. In one embodiment, the humanized or human anti-CD3 binding domain is a scFv, and a light chain variable region comprising an amino acid sequence described herein, is attached to a heavy chain variable region comprising an amino acid sequence described herein, via a scFv linker. The light chain variable region and heavy chain variable region of a scFv can be, e.g., in any of the following orientations: light chain variable region-scFv linker-heavy chain variable region or heavy chain variable region-scFv linker-light chain variable region.

[0057] In some instances, scFvs which bind to CD3 are prepared according to known methods. For example, scFv molecules can be produced by linking VH and VL regions together using flexible polypeptide linkers. The scFv molecules comprise a scFv linker (e.g., a Ser-Gly linker) with an optimized length and/or amino acid composition. Accordingly, in some embodiments, the length of the scFv linker is such that the VH or VL domain can associate intermolecularly with the other variable domain to form the CD3 binding site. In certain embodiments, such scFv linkers are "short", i.e. consist of 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12 amino acid residues. Thus, in certain instances, the scFv linkers consist of about 12 or less amino acid residues. In the case of 0 amino acid residues, the scFv linker is a peptide bond. In some embodiments, these scFv linkers consist of about 3 to about 15, for example 8, 9 or 10 contiguous amino acid residues. Regarding the amino acid composition of the scFv linkers, peptides are selected that confer flexibility, do not interfere with the variable domains as well as allow inter-chain folding to bring the two variable domains together to form a functional CD3 binding site. For example, scFv linkers comprising glycine and serine residues generally provide protease resistance. In some embodiments, linkers in a scFv comprise glycine and serine residues. The amino acid sequence of the scFv linkers can be optimized, for example, by phage-display methods to improve the CD3 binding and production yield of the scFv. Examples of peptide scFv linkers suitable for linking a variable light chain domain and a variable heavy chain domain in a scFv include but are not limited to (GS).sub.n (SEQ ID NO: 153), (GGS).sub.n (SEQ ID NO: 154), (GGGS).sub.n (SEQ ID NO: 155), (GGSG).sub.n (SEQ ID NO: 156), (GGSGG).sub.n (SEQ ID NO: 157), or (GGGGS).sub.n (SEQ ID NO: 158), wherein n is 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10. In one embodiment, the scFv linker can be (GGGGS).sub.4 (SEQ ID NO: 159) or (GGGGS).sub.3 (SEQ ID NO: 160). Variation in the linker length may retain or enhance activity, giving rise to superior efficacy in activity studies.

[0058] In some embodiments, CD3 binding domain of PSMA trispecific antigen-binding protein has an affinity to CD3 on CD3 expressing cells with a K.sub.D of 1000 nM or less, 500 nM or less, 200 nM or less, 100 nM or less, 80 nM or less, 50 nM or less, 20 nM or less, 10 nM or less, 5 nM or less, 1 nM or less, or 0.5 nM or less. In some embodiments, the CD3 binding domain of PSMA trispecific antigen-binding protein has an affinity to CD3.epsilon., .gamma., or .delta. with a K.sub.D of 1000 nM or less, 500 nM or less, 200 nM or less, 100 nM or less, 80 nM or less, 50 nM or less, 20 nM or less, 10 nM or less, 5 nM or less, 1 nM or less, or 0.5 nM or less. In further embodiments, CD3 binding domain of PSMA trispecific antigen-binding protein has low affinity to CD3, i.e., about 100 nM or greater.

[0059] The affinity to bind to CD3 can be determined, for example, by the ability of the PSMA trispecific antigen-binding protein itself or its CD3 binding domain to bind to CD3 coated on an assay plate; displayed on a microbial cell surface; in solution; etc. The binding activity of the PSMA trispecific antigen-binding protein itself or its CD3 binding domain of the present disclosure to CD3 can be assayed by immobilizing the ligand (e.g., CD3) or the PSMA trispecific antigen-binding protein itself or its CD3 binding domain, to a bead, substrate, cell, etc. Agents can be added in an appropriate buffer and the binding partners incubated for a period of time at a given temperature. After washes to remove unbound material, the bound protein can be released with, for example, SDS, buffers with a high pH, and the like and analyzed, for example, by Surface Plasmon Resonance (SPR).

[0060] In some embodiments, CD3 binding domains described herein comprise a polypeptide having a sequence described in Table 7 (SEQ ID NO: 1-88) and subsequences thereof. In some embodiments, the CD3 binding domain comprises a polypeptide having at least 70%-95% or more homology to a sequence described in Table 7 (SEQ ID NO: 1-88). In some embodiments, the CD3 binding domain comprises a polypeptide having at least 70%, 75%, 80%, 85%, 90%, 95%, or more homology to a sequence described in Table 7 (SEQ ID NO: 1-88). In some embodiments, the CD3 binding domain has a sequence comprising at least a portion of a sequence described in Table 7 (SEQ ID NO: 1-88). In some embodiments, the CD3 binding domain comprises a polypeptide comprising one or more of the sequences described in Table 7 (SEQ ID NO: 1-88).

[0061] In certain embodiments, CD3 binding domain comprises an scFv with a heavy chain CDR1 comprising SEQ ID NO: 16, and 22-33. In certain embodiments, CD3 binding domain comprises an scFv with a heavy chain CDR2 comprising SEQ ID NO: 17, and 34-43. In certain embodiments, CD3 binding domain comprises an scFv with a heavy chain CDR3 comprising SEQ ID NO: 18, and 44-53. In certain embodiments, CD3 binding domain comprises an scFv with a light chain CDR1 comprising SEQ ID NO: 19, and 54-66. In certain embodiments, CD3 binding domain comprises an scFv with a light chain CDR2 comprising SEQ ID NO: 20, and 67-79. In certain embodiments, CD3 binding domain comprises an scFv with a light chain CDR3 comprising SEQ ID NO: 21, and 80-86.

Half-Life Extension Domain

[0062] Contemplated herein are domains which extend the half-life of an antigen-binding domain. Such domains are contemplated to include but are not limited to HSA binding domains, Fc domains, small molecules, and other half-life extension domains known in the art.

[0063] Human serum albumin (HSA) (molecular mass .about.67 kDa) is the most abundant protein in plasma, present at about 50 mg/ml (600 .mu.M), and has a half-life of around 20 days in humans. HSA serves to maintain plasma pH, contributes to colloidal blood pressure, functions as carrier of many metabolites and fatty acids, and serves as a major drug transport protein in plasma.

[0064] Noncovalent association with albumin extends the elimination half-time of short lived proteins. For example, a recombinant fusion of an albumin binding domain to a Fab fragment resulted in an in vivo clearance of 25- and 58-fold and a half-life extension of 26- and 37-fold when administered intravenously to mice and rabbits respectively as compared to the administration of the Fab fragment alone. In another example, when insulin is acylated with fatty acids to promote association with albumin, a protracted effect was observed when injected subcutaneously in rabbits or pigs. Together, these studies demonstrate a linkage between albumin binding and prolonged action.

[0065] In one aspect, the PSMA targeting trispecific proteins described herein comprise a half-life extension domain, for example a domain which specifically binds to HSA. In some embodiments, the HSA binding domain of PSMA trispecific antigen-binding protein can be any domain that binds to HSA including but not limited to domains from a monoclonal antibody, a polyclonal antibody, a recombinant antibody, a human antibody, a humanized antibody. In some embodiments, the HSA binding domain is a single chain variable fragments (scFv), single-domain antibody such as a heavy chain variable domain (VH), a light chain variable domain (VL) and a variable domain (VHH) of camelid derived single domain antibody, peptide, ligand or small molecule entity specific for HSA. In certain embodiments, the HSA binding domain is a single-domain antibody. In other embodiments, the HSA binding domain is a peptide. In further embodiments, the HSA binding domain is a small molecule. It is contemplated that the HSA binding domain of PSMA trispecific antigen-binding protein is fairly small and no more than 25 kD, no more than 20 kD, no more than 15 kD, or no more than 10 kD in some embodiments. In certain instances, the HSA binding is 5 kD or less if it is a peptide or small molecule entity.

[0066] The half-life extension domain of PSMA trispecific antigen-binding protein provides for altered pharmacodynamics and pharmacokinetics of the PSMA trispecific antigen-binding protein itself. As above, the half-life extension domain extends the elimination half-time. The half-life extension domain also alters pharmacodynamic properties including alteration of tissue distribution, penetration, and diffusion of the trispecific antigen-binding protein. In some embodiments, the half-life extension domain provides for improved tissue (including tumor) targeting, tissue distribution, tissue penetration, diffusion within the tissue, and enhanced efficacy as compared with a protein without an half-life extension domain. In one embodiment, therapeutic methods effectively and efficiently utilize a reduced amount of the trispecific antigen-binding protein, resulting in reduced side effects, such as reduced non-tumor cell cytotoxicity.

[0067] Further, the binding affinity of the half-life extension domain can be selected so as to target a specific elimination half-time in a particular trispecific antigen-binding protein. Thus, in some embodiments, the half-life extension domain has a high binding affinity. In other embodiments, the half-life extension domain has a medium binding affinity. In yet other embodiments, the half-life extension domain has a low or marginal binding affinity. Exemplary binding affinities include K.sub.D concentrations at 10 nM or less (high), between 10 nM and 100 nM (medium), and greater than 100 nM (low). As above, binding affinities to HSA are determined by known methods such as Surface Plasmon Resonance (SPR).

[0068] In some embodiments, HSA binding domains described herein comprise a polypeptide having a sequence described in Table 8 (SEQ ID NO: 89-112) and subsequences thereof. In some embodiments, the HSA binding domain comprises a polypeptide having at least 70%-95% or more homology to a sequence described in Table 8 (SEQ ID NO: 89-112). In some embodiments, the HSA binding domain comprises a polypeptide having at least 70%, 75%, 80%, 85%, 90%, 95%, or more homology to a sequence described in Table 8 (SEQ ID NO: 89-112). In some embodiments, the HSA binding domain has a sequence comprising at least a portion of a sequence described in Table 8 (SEQ ID NO: 89-112). In some embodiments, the HSA binding domain comprises a polypeptide comprising one or more of the sequences described in Table 8 (SEQ ID NO: 89-112).

[0069] In some embodiments, HSA binding domains described herein comprise a single domain antibody with a CDR1 comprising SE ID NO: 96, and 99-101. In some embodiments, HSA binding domains described herein comprise a single domain antibody with a CDR1 comprising SE ID NO: 97, and 102-107. In some embodiments, HSA binding domains described herein comprise a single domain antibody with a CDR1 comprising SE ID NO: 98, 108 and 109.

Prostate Specific Membrane Antigen (PSMA) Binding Domain

[0070] Prostate specific membrane antigen (PSMA) is a 100 kD Type II membrane glycoprotein expressed in prostate tissues having sequence identity with the transferrin receptor with NAALADase activity. PSMA is expressed in increased amounts in prostate cancer, and elevated levels of PSMA are also detectable in the sera of these patients. PSMA expression increases with disease progression, becoming highest in metastatic, hormone-refractory disease for which there is no present therapy.

[0071] In addition to the described CD3 and half-life extension domains, the PSMA targeting trispecific proteins described herein also comprise a domain that binds to PSMA. The design of the PSMA targeting trispecific proteins described herein allows the binding domain to PSMA to be flexible in that the binding domain to PSMA can be any type of binding domain, including but not limited to, domains from a monoclonal antibody, a polyclonal antibody, a recombinant antibody, a human antibody, a humanized antibody. In some embodiments, the binding domain to PSMA is a single chain variable fragments (scFv), single-domain antibody such as a heavy chain variable domain (VH), a light chain variable domain (VL) and a variable domain (VHH) of camelid derived single domain antibody. In other embodiments, the binding domain to PSMA is a non-Ig binding domain, i.e., antibody mimetic, such as anticalins, affilins, affibody molecules, affimers, affitins, alphabodies, avimers, DARPins, fynomers, kunitz domain peptides, and monobodies. In further embodiments, the binding domain to PSMA is a ligand or peptide that binds to or associates with PSMA. In yet further embodiments, the binding domain to PSMA is a knottin. In yet further embodiments, the binding domain to PSMA is a small molecular entity.

[0072] In some embodiments, the PSMA binding domain comprises the following formula: f1-r1-f2-r2-f3-r3-f4, wherein r1, r2, and r3 are complementarity determining regions CDR1, CDR2, and CDR3, respectively, and f1, f2, f3, and f4 are framework residues, and wherein r1 comprises SEQ ID No. 114, SEQ ID No. 115, SEQ ID No. 116, or SEQ ID NOL 125, r2 comprises SEQ ID No. 117, SEQ ID NO. 118, SEQ ID No. 119, SEQ ID No. 120, SEQ ID No. 121, SEQ ID No. 122, SEQ ID No. 123, or SEQ ID NO: 126, and r3 comprises SEQ ID No. 124, or SEQ ID NO: 127.

[0073] In some embodiments, the PSMA binding domain comprises a CDR1, CDR2, and CDR3, wherein (a) the amino acid sequence of CDR1 is as set forth in SEQ ID No. 162 (RFMISX.sub.1YX.sub.2MH), (b) the amino acid sequence of CDR2 is as set forth in SEQ ID No. 163 (X.sub.3INPAX4X.sub.5TDYAEX6VKG), and (c) the amino acid sequence of CDR3 is as set forth in SEQ ID No. 164 (DX.sub.7YGY). In some embodiments, the amino acid residues X.sub.1, X.sub.2, X.sub.3, X.sub.4, X.sub.5, X.sub.6, and X.sub.7 are independently selected from glutamic acid, proline, serine, histidine, threonine, aspartic acid, glycine, lysine, threonine, glutamine, and tyrosine. In some embodiments, X.sub.1 is proline. In some embodiments, X.sub.2 is histidine. In some embodiments, X.sub.3 is aspartic acid. In some embodiments, X.sub.4 is lysine. In some embodiments, X.sub.5 is glutamine. In some embodiments, X.sub.6 is tyrosine. In some embodiments, X.sub.7 is serine. The PSMA binding protein of the present disclosure may in some embodiments comprise CDR1, CDR2, and CDR3 sequences wherein X.sub.1 is glutamic acid, X.sub.2 is histidine, X.sub.3 is aspartic acid, X.sub.4 is glycine, X.sub.5 is threonine, X.sub.6 is serine, and X.sub.7 is serine.

[0074] In some embodiments, the PSMA binding domain comprises a CDR1, CDR2, and CDR3, wherein (a) the amino acid sequence of CDR1 is as set forth in SEQ ID No. 162 (RFMISX.sub.1YX.sub.2MH), (b) the amino acid sequence of CDR2 is as set forth in SEQ ID No. 163 (X.sub.3INPAX.sub.4X.sub.5TDYAEX.sub.6VKG), and (c) the amino acid sequence of CDR3 is as set forth in SEQ ID No. 164 (DX.sub.7YGY), wherein X1 is proline. In some embodiments, the PSMA binding domain comprises a CDR1, CDR2, and CDR3, wherein (a) the amino acid sequence of CDR1 is as set forth in SEQ ID No. 162 (RFMISX.sub.1YX.sub.2MH), (b) the amino acid sequence of CDR2 is as set forth in SEQ ID No. 163 (X.sub.3INPAX.sub.4X.sub.5TDYAEX.sub.6VKG), and (c) the amino acid sequence of CDR3 is as set forth in SEQ ID No. 164 (DX.sub.7YGY), wherein X5 is glutamine. In some embodiments, the PSMA binding domain comprises a CDR1, CDR2, and CDR3, wherein (a) the amino acid sequence of CDR1 is as set forth in SEQ ID No. 162 (RFMISX.sub.1YX.sub.2MH), (b) the amino acid sequence of CDR2 is as set forth in SEQ ID No. 163 (X.sub.3INPAX.sub.4X.sub.5TDYAEX.sub.6VKG), and (c) the amino acid sequence of CDR3 is as set forth in SEQ ID No. 164 (DX.sub.7YGY), wherein X.sub.6 is tyrosine. In some embodiments, the PSMA binding domain comprises a CDR1, CDR2, and CDR3, wherein (a) the amino acid sequence of CDR1 is as set forth in SEQ ID No. 162 (RFMISX.sub.1YX.sub.2MH), (b) the amino acid sequence of CDR2 is as set forth in SEQ ID No. 163 (X.sub.3INPAX.sub.4X.sub.5TDYAEX.sub.6VKG), and (c) the amino acid sequence of CDR3 is as set forth in SEQ ID No. 164 (DX.sub.7YGY), wherein X.sub.4 is lysine, and X.sub.7 is serine. In some embodiments, the PSMA binding domain comprises a CDR1, CDR2, and CDR3, wherein (a) the amino acid sequence of CDR1 is as set forth in SEQ ID No. 162 (RFMISX.sub.1YX.sub.2MH), (b) the amino acid sequence of CDR2 is as set forth in SEQ ID No. 163 (X.sub.3INPAX.sub.4X.sub.5TDYAEX.sub.6VKG), and (c) the amino acid sequence of CDR3 is as set forth in SEQ ID No. 164 (DX.sub.7YGY), wherein X.sub.2 is histidine, X.sub.3 is aspartic acid, X.sub.4 is lysine, and X.sub.7 is serine. In some embodiments, the PSMA binding domain comprises a CDR1, CDR2, and CDR3, wherein (a) the amino acid sequence of CDR1 is as set forth in SEQ ID No. 162 (RFMISX.sub.1YX.sub.2MH), (b) the amino acid sequence of CDR2 is as set forth in SEQ ID No. 163 (X.sub.3INPAX.sub.4X.sub.5TDYAEX.sub.6VKG), and (c) the amino acid sequence of CDR3 is as set forth in SEQ ID No. 164 (DX.sub.7YGY), wherein X.sub.1 is proline, X.sub.2 is histidine, X.sub.3 is aspartic acid, and X.sub.7 is serine. In some embodiments, the PSMA binding domain comprises a CDR1, CDR2, and CDR3, wherein (a) the amino acid sequence of CDR1 is as set forth in SEQ ID No. 162 (RFMISX.sub.1YX.sub.2MH), (b) the amino acid sequence of CDR2 is as set forth in SEQ ID No. 163 (X.sub.3INPAX.sub.4X.sub.5TDYAEX.sub.6VKG), and (c) the amino acid sequence of CDR3 is as set forth in SEQ ID No. 164 (DX.sub.7YGY), wherein X.sub.2 is histidine, X.sub.3 is aspartic acid, X.sub.5 is glutamine, and X.sub.7 is serine. In some embodiments, the PSMA binding domain comprises a CDR1, CDR2, and CDR3, wherein (a) the amino acid sequence of CDR1 is as set forth in SEQ ID No. 162 (RFMISX.sub.1YX.sub.2MH), (b) the amino acid sequence of CDR2 is as set forth in SEQ ID No. 163 (X.sub.3INPAX.sub.4X.sub.5TDYAEX.sub.6VKG), and (c) the amino acid sequence of CDR3 is as set forth in SEQ ID No. 164 (DX.sub.7YGY), wherein X.sub.2 is histidine, X.sub.3 is aspartic acid, X.sub.6 is tyrosine, and X.sub.7 is serine. In some embodiments, the PSMA binding domain comprises a CDR1, CDR2, and CDR3, wherein (a) the amino acid sequence of CDR1 is as set forth in SEQ ID No. 162 (RFMISX.sub.1YX.sub.2MH), (b) the amino acid sequence of CDR2 is as set forth in SEQ ID No. 163 (X.sub.3INPAX.sub.4X.sub.5TDYAEX.sub.6VKG), and (c) the amino acid sequence of CDR3 is as set forth in SEQ ID No. 164 (DX.sub.7YGY), wherein X.sub.2 is histidine, X.sub.3 is aspartic acid, and X.sub.7 is serine.

[0075] The PSMA binding domain of the present disclosure may in some embodiments comprise CDR1, CDR2, and CDR3 sequences wherein X.sub.1 is glutamic acid, X.sub.2 is histidine, X.sub.3 is threonine, X.sub.4 is glycine, X.sub.5 is threonine, X.sub.6 is serine, and X.sub.7 is serine. The PSMA binding domain of the present disclosure may in some embodiments comprise CDR1, CDR2, and CDR3 sequences wherein X.sub.1 is glutamic acid, X.sub.2 is histidine, X.sub.3 is threonine, X.sub.4 is glycine, X.sub.5 is threonine, X.sub.6 is serine, and X.sub.7 is serine. The PSMA binding domain of the present disclosure may in some embodiments comprise CDR1, CDR2, and CDR3 sequences wherein X.sub.1 is glutamic acid, X.sub.2 is serine, X.sub.3 is threonine, X.sub.4 is lysine, X.sub.5 is threonine, X.sub.6 is serine, and X.sub.7 is serine. The PSMA binding domain of the present disclosure may in some embodiments comprise CDR1, CDR2, and CDR3 sequences wherein X.sub.1 is proline, X.sub.2 is serine, X.sub.3 is threonine, X.sub.4 is glycine, X.sub.5 is threonine, X6 is serine, and X7 is glycine. The PSMA binding domain of the present disclosure may in some embodiments comprise CDR1, CDR2, and CDR3 sequences wherein X.sub.1 is glutamic acid, X.sub.2 is serine, X.sub.3 is threonine, X.sub.4 is glycine, X.sub.5 is glutamine, X.sub.6 is serine, and X.sub.7 is glycine. The PSMA binding domain of the present disclosure may in some embodiments comprise CDR1, CDR2, and CDR3 sequences wherein X.sub.1 is glutamic acid, X.sub.2 is serine, X.sub.3 is threonine, X.sub.4 is glycine, X.sub.5 is threonine, X.sub.6 is tyrosine, and X.sub.7 is glycine. The PSMA binding domain of the present disclosure may in some embodiments comprise CDR1, CDR2, and CDR3 sequences wherein X.sub.1 is glutamic acid, X.sub.2 is histidine, X.sub.3 is aspartic acid, X.sub.4 is lysine, X.sub.5 is threonine, X.sub.6 is serine, and X.sub.7 is serine. The PSMA binding domain of the present disclosure may in some embodiments comprise CDR1, CDR2, and CDR3 sequences wherein X.sub.1 is proline, X.sub.2 is histidine, X.sub.3 is aspartic acid, X.sub.4 is glycine, X.sub.5 is threonine, X.sub.6 is serine, and X.sub.7 is serine. The PSMA binding domain of the present disclosure may in some embodiments comprise CDR1, CDR2, and CDR3 sequences wherein X.sub.1 is glutamic acid, X.sub.2 is histidine, X.sub.3 is aspartic acid, X.sub.4 is glutamine, X.sub.5 is threonine, X.sub.6 is serine, and X.sub.7 is serine. The PSMA binding domain of the present disclosure may in some embodiments comprise CDR1, CDR2, and CDR3 sequences wherein X.sub.1 is glutamic acid, X.sub.2 is histidine, X.sub.3 is aspartic acid, X.sub.4 is glycine, X.sub.5 is threonine, X.sub.6 is tyrosine, and X.sub.7 is serine. The PSMA binding domain of the present disclosure may in some embodiments comprise CDR1, CDR2, and CDR3 sequences wherein X.sub.2 is histidine, and X.sub.7 is serine. Exemplary framework sequences are disclosed as SEQ ID NO: 165-168.

[0076] In some embodiments, PSMA binding domains described herein comprise a polypeptide having a sequence described in Table 9 (SEQ ID NO: 113-140) and subsequences thereof. In some embodiments, the HSA binding domain comprises a polypeptide having at least 70%-95% or more homology to a sequence described in Table 9 (SEQ ID NO: 113-140). In some embodiments, the HSA binding domain comprises a polypeptide having at least 70%, 75%, 80%, 85%, 90%, 95%, or more homology to a sequence described in Table 9 (SEQ ID NO: 113-140). In some embodiments, the HSA binding domain has a sequence comprising at least a portion of a sequence described in Table 9 (SEQ ID NO: 113-140). In some embodiments, the HSA binding domain comprises a polypeptide comprising one or more of the sequences described in Table 9 (SEQ ID NO: 113-140).

[0077] In some embodiments, PSMA binding domains described herein comprise a single domain antibody with a CDR1 comprising SE ID NO: 114-116, and 125. In some embodiments, PSMA binding domains described herein comprise a single domain antibody with a CDR1 comprising SEQ ID NO: 117-123, and 126. In some embodiments, PSMA binding domains described herein comprise a single domain antibody with a CDR1 comprising SE ID NO: 124 and 127.

PSMA Trispecific Protein Modifications

[0078] The PSMA targeting trispecific proteins described herein encompass derivatives or analogs in which (i) an amino acid is substituted with an amino acid residue that is not one encoded by the genetic code, (ii) the mature polypeptide is fused with another compound such as polyethylene glycol, or (iii) additional amino acids are fused to the protein, such as a leader or secretory sequence or a sequence for purification of the protein.

[0079] Typical modifications include, but are not limited to, acetylation, acylation, ADP-ribosylation, amidation, covalent attachment of flavin, covalent attachment of a heme moiety, covalent attachment of a nucleotide or nucleotide derivative, covalent attachment of a lipid or lipid derivative, covalent attachment of phosphatidylinositol, cross-linking, cyclization, disulfide bond formation, demethylation, formation of covalent crosslinks, formation of cystine, formation of pyroglutamate, formylation, gamma carboxylation, glycosylation, GPI anchor formation, hydroxylation, iodination, methylation, myristoylation, oxidation, proteolytic processing, phosphorylation, prenylation, racemization, selenoylation, sulfation, transfer-RNA mediated addition of amino acids to proteins such as arginylation, and ubiquitination.

[0080] Modifications are made anywhere in PSMA targeting trispecific proteins described herein, including the peptide backbone, the amino acid side-chains, and the amino or carboxyl termini. Certain common peptide modifications that are useful for modification of PSMA targeting trispecific proteins include glycosylation, lipid attachment, sulfation, gamma-carboxylation of glutamic acid residues, hydroxylation, blockage of the amino or carboxyl group in a polypeptide, or both, by a covalent modification, and ADP-ribosylation.

Polynucleotides Encoding PSMA Targeting Trispecific Proteins

[0081] Also provided, in some embodiments, are polynucleotide molecules encoding a PSMA trispecific antigen-binding protein described herein. In some embodiments, the polynucleotide molecules are provided as a DNA construct. In other embodiments, the polynucleotide molecules are provided as a messenger RNA transcript.

[0082] The polynucleotide molecules are constructed by known methods such as by combining the genes encoding the three binding domains either separated by peptide linkers or, in other embodiments, directly linked by a peptide bond, into a single genetic construct operably linked to a suitable promoter, and optionally a suitable transcription terminator, and expressing it in bacteria or other appropriate expression system such as, for example CHO cells. In the embodiments where the PSMA binding domain is a small molecule, the polynucleotides contain genes encoding the CD3 binding domain and the half-life extension domain. In the embodiments where the half-life extension domain is a small molecule, the polynucleotides contain genes encoding the domains that bind to CD3 and PSMA. Depending on the vector system and host utilized, any number of suitable transcription and translation elements, including constitutive and inducible promoters, may be used. The promoter is selected such that it drives the expression of the polynucleotide in the respective host cell.

[0083] In some embodiments, the polynucleotide is inserted into a vector, preferably an expression vector, which represents a further embodiment. This recombinant vector can be constructed according to known methods. Vectors of particular interest include plasmids, phagemids, phage derivatives, virii (e.g., retroviruses, adenoviruses, adeno-associated viruses, herpes viruses, lentiviruses, and the like), and cosmids.

[0084] A variety of expression vector/host systems may be utilized to contain and express the polynucleotide encoding the polypeptide of the described trispecific antigen-binding protein. Examples of expression vectors for expression in E. coli are pSKK (Le Gall et al., J Immunol Methods. (2004) 285(1):111-27) or pcDNA5 (Invitrogen) for expression in mammalian cells.

[0085] Thus, the PSMA targeting trispecific proteins as described herein, in some embodiments, are produced by introducing a vector encoding the protein as described above into a host cell and culturing said host cell under conditions whereby the protein domains are expressed, may be isolated and, optionally, further purified.

Pharmaceutical Compositions

[0086] Also provided, in some embodiments, are pharmaceutical compositions comprising a PSMA trispecific antigen-binding protein described herein, a vector comprising the polynucleotide encoding the polypeptide of the PSMA targeting trispecific proteins or a host cell transformed by this vector and at least one pharmaceutically acceptable carrier. The term "pharmaceutically acceptable carrier" includes, but is not limited to, any carrier that does not interfere with the effectiveness of the biological activity of the ingredients and that is not toxic to the patient to whom it is administered. Examples of suitable pharmaceutical carriers are well known in the art and include phosphate buffered saline solutions, water, emulsions, such as oil/water emulsions, various types of wetting agents, sterile solutions etc. Such carriers can be formulated by conventional methods and can be administered to the subject at a suitable dose. Preferably, the compositions are sterile. These compositions may also contain adjuvants such as preservative, emulsifying agents and dispersing agents. Prevention of the action of microorganisms may be ensured by the inclusion of various antibacterial and antifungal agents.

[0087] In some embodiments of the pharmaceutical compositions, the PSMA targeting trispecific proteins described herein are encapsulated in nanoparticles. In some embodiments, the nanoparticles are fullerenes, liquid crystals, liposome, quantum dots, superparamagnetic nanoparticles, dendrimers, or nanorods. In other embodiments of the pharmaceutical compositions, the PSMA trispecific antigen-binding protein is attached to liposomes. In some instances, the PSMA trispecific antigen-binding protein are conjugated to the surface of liposomes. In some instances, the PSMA trispecific antigen-binding protein are encapsulated within the shell of a liposome. In some instances, the liposome is a cationic liposome.

[0088] The PSMA targeting trispecific proteins described herein are contemplated for use as a medicament. Administration is effected by different ways, e.g. by intravenous, intraperitoneal, subcutaneous, intramuscular, topical or intradermal administration. In some embodiments, the route of administration depends on the kind of therapy and the kind of compound contained in the pharmaceutical composition. The dosage regimen will be determined by the attending physician and other clinical factors. Dosages for any one patient depends on many factors, including the patient's size, body surface area, age, sex, the particular compound to be administered, time and route of administration, the kind of therapy, general health and other drugs being administered concurrently. An "effective dose" refers to amounts of the active ingredient that are sufficient to affect the course and the severity of the disease, leading to the reduction or remission of such pathology and may be determined using known methods.

Methods of Treatment

[0089] Also provided herein, in some embodiments, are methods and uses for stimulating the immune system of an individual in need thereof comprising administration of a PSMA targeting trispecific protein described herein. In some instances, the administration of a PSMA targeting trispecific protein described herein induces and/or sustains cytotoxicity towards a cell expressing PSMA. In some instances, the cell expressing PSMA is a cancer cell.

[0090] Also provided herein are methods and uses for a treatment of a disease, disorder or condition associated with PSMA comprising administering to an individual in need thereof a PSMA targeting trispecific protein described herein. Diseases, disorders or conditions associated with PSMA include, but are not limited to, a proliferative disease or a tumorous disease. In one embodiment, the disease, disorder or condition associated with PSMA is prostate cancer. In another embodiment, the disease, disorder, or condition associated with PSMA is renal cancer.

[0091] In some embodiments, the prostate cancer is an advanced stage prostate cancer. In some embodiments, the prostate cancer is drug resistant. In some embodiments, the prostate cancer is anti-androgen drug resistant. In some embodiments, the prostate cancer is metastatic. In some embodiments, the prostate cancer is metastatic and drug resistant (e.g., anti-androgen drug resistant). In some embodiments, the prostate cancer is castration resistant. In some embodiments, the prostate cancer is metastatic and castration resistant. In some embodiments, the prostate cancer is enzalutamide resistant. In some embodiments, the prostate cancer is enzalutamide and arbiraterone resistant. In some embodiments, the prostate cancer is enzalutamide, arbiraterone, and bicalutamide resistant. In some embodiments, the prostate cancer is docetaxel resistant. In some of these embodiments, the prostate cancer is enzalutamide, arbiraterone, bicalutamide, and docetaxel resistant.

[0092] In some embodiments, administering a PSMA targeting trispecific protein described herein inhibits prostate cancer cell growth; inhibits prostate cancer cell migration; inhibits prostate cancer cell invasion; ameliorates the symptoms of prostate cancer; reduces the size of a prostate cancer tumor; reduces the number of prostate cancer tumors; reduces the number of prostate cancer cells; induces prostate cancer cell necrosis, pyroptosis, oncosis, apoptosis, autophagy, or other cell death; or enhances the therapeutic effects of a compound selected from the group consisting of enzalutamide, abiraterone, docetaxel, bicalutamide, and any combinations thereof.

[0093] In some embodiments, the method comprises inhibiting prostate cancer cell growth by administering a PSMA targeting trispecific protein described herein. In some embodiments, the method comprises inhibiting prostate cancer cell migration by administering a PSMA targeting trispecific protein described herein. In some embodiments, the method comprises inhibiting prostate cancer cell invasion by administering a PSMA targeting trispecific protein described herein. In some embodiments, the method comprises ameliorating the symptoms of prostate cancer by administering a PSMA targeting trispecific protein described herein. In some embodiments, the method comprises reducing the size of a prostate cancer tumor by administering a PSMA targeting trispecific protein described herein. In some embodiments, the method comprises reducing the number of prostate cancer tumors by administering a PSMA targeting trispecific protein described herein. In some embodiments, the method comprises reducing the number of prostate cancer cells by administering a PSMA targeting trispecific protein described herein. In some embodiments, the method comprises inducing prostate cancer cell necrosis, pyroptosis, oncosis, apoptosis, autophagy, or other cell death by administering a PSMA targeting trispecific protein described herein.

[0094] As used herein, in some embodiments, "treatment" or "treating" or "treated" refers to therapeutic treatment wherein the object is to slow (lessen) an undesired physiological condition, disorder or disease, or to obtain beneficial or desired clinical results. For the purposes described herein, beneficial or desired clinical results include, but are not limited to, alleviation of symptoms; diminishment of the extent of the condition, disorder or disease; stabilization (i.e., not worsening) of the state of the condition, disorder or disease; delay in onset or slowing of the progression of the condition, disorder or disease; amelioration of the condition, disorder or disease state; and remission (whether partial or total), whether detectable or undetectable, or enhancement or improvement of the condition, disorder or disease. Treatment includes eliciting a clinically significant response without excessive levels of side effects. Treatment also includes prolonging survival as compared to expected survival if not receiving treatment. In other embodiments, "treatment" or "treating" or "treated" refers to prophylactic measures, wherein the object is to delay onset of or reduce severity of an undesired physiological condition, disorder or disease, such as, for example is a person who is predisposed to a disease (e.g., an individual who carries a genetic marker for a disease such as prostate cancer).

[0095] In some embodiments of the methods described herein, the PSMA targeting trispecific proteins are administered in combination with an agent for treatment of the particular disease, disorder or condition. Agents include but are not limited to, therapies involving antibodies, small molecules (e.g., chemotherapeutics), hormones (steroidal, peptide, and the like), radiotherapies (.gamma.-rays, X-rays, and/or the directed delivery of radioisotopes, microwaves, UV radiation and the like), gene therapies (e.g., antisense, retroviral therapy and the like) and other immunotherapies. In some embodiments, the PSMA targeting trispecific proteins are administered in combination with anti-diarrheal agents, anti-emetic agents, analgesics, opioids and/or non-steroidal anti-inflammatory agents. In some embodiments, the PSMA targeting trispecific proteins are administered before, during, or after surgery.

Certain Definitions

[0096] As used herein, "elimination half-time" is used in its ordinary sense, as is described in Goodman and Gillman's The Pharmaceutical Basis of Therapeutics 21-25 (Alfred Goodman Gilman, Louis S. Goodman, and Alfred Gilman, eds., 6th ed. 1980). Briefly, the term is meant to encompass a quantitative measure of the time course of drug elimination. The elimination of most drugs is exponential (i.e., follows first-order kinetics), since drug concentrations usually do not approach those required for saturation of the elimination process. The rate of an exponential process may be expressed by its rate constant, k, which expresses the fractional change per unit of time, or by its half-time, t.sub.1/2 the time required for 50% completion of the process. The units of these two constants are time.sup.- time, respectively. A first-order rate constant and the half-time of the reaction are simply related (k.times.t.sub.1/2=0.693) and may be interchanged accordingly. Since first-order elimination kinetics dictates that a constant fraction of drug is lost per unit time, a plot of the log of drug concentration versus time is linear at all times following the initial distribution phase (i.e. after drug absorption and distribution are complete). The half-time for drug elimination can be accurately determined from such a graph.

[0097] As used herein, the phrase "prostate cancer" or "advanced stage prostate cancer" includes a class of prostate cancers that has progressed beyond early stages of the disease. Typically, advanced stage prostate cancers are associated with a poor prognosis. Types of advanced stage prostate cancers include, but are not limited to, metastatic prostate cancer, drug-resistant prostate cancer such as anti-androgen-resistant prostate cancer (e.g., enzalutamide-resistant prostate cancer, abiraterone-resistant prostate cancer, bicalutamide-resistant prostate cancer, and the like), hormone refractory prostate cancer, castration-resistant prostate cancer, metastatic castration-resistant prostate cancer, docetaxel-resistant prostate cancer, androgen receptor splice variant-7 (AR-V7)-induced drug-resistant prostate cancer such as AR-V7-induced anti-androgen-resistant prostate cancer (e.g., AR-V7-induced enzalutamide-resistant prostate cancer), aldo-keto reductase family 1 member C3 (AKR1C3)-induced drug-resistant prostate cancer such as AKR1C3-induced anti-androgen-resistant prostate cancer (e.g., AKR1C3-induced enzalutamide-resistant prostate cancer), and combinations thereof. In some instances, the advanced stage prostate cancers do not generally respond, or are resistant, to treatment with one or more of the following conventional prostate cancer therapies: enzalutamide, arbiraterone, bicalutamide, and docetaxel. Compounds, compositions, and methods of the present disclosure are provided for treating prostate cancer, such as advanced stage prostate cancer, including any one or more (e.g., two, three, four, five, six, seven, eight, nine, ten, or more) of the types of advanced stage prostate cancers disclosed herein.

EXAMPLES

Example 1: Methods to Assess Binding and Cytotoxic Activities of Trispecific Antigen Binding Molecules

[0098] Protein Production

[0099] Sequences of trispecific molecules were cloned into mammalian expression vector pcDNA 3.4 (Invitrogen) preceded by a leader sequence and followed by a 6.times. Histidine Tag (SEQ ID NO: 161). Expi293F cells (Life Technologies A14527) were maintained in suspension in Optimum Growth Flasks (Thomson) between 0.2 to 8.times.1e6 cells/ml in Expi293 media. Purified plasmid DNA was transfected into Expi293 cells in accordance with Expi293 Expression System Kit (Life Technologies, A14635) protocols, and maintained for 4-6 days post transfection. Conditioned media was partially purified by affinity and desalting chromatography. Trispecific proteins were subsequently polished by ion exchange or, alternatively, concentrated with Amicon Ultra centrifugal filtration units (EMD Millipore), applied to Superdex 200 size exclusion media (GE Healthcare) and resolved in a neutral buffer containing excipients. Fraction pooling and final purity were assessed by SDS-PAGE and analytical SEC.

[0100] Affinity Measurements

[0101] The affinities of the all binding domains molecules were measured by biolayer inferometry using an Octet instrument.

[0102] PSMA affinities were measured by loading human PSMA-Fc protein (100 nM) onto anti-human IgG Fc biosensors for 120 seconds, followed by a 60 second baseline, after which associations were measured by incubating the sensor tip in a dilution series of the trispecific molecules for 180 seconds, followed by dissociation for 50 seconds. EGFR and CD3 affinities were measured by loading human EGFR-Fc protein or human CD3-Flag-Fc protein, respectively, (100 nM) onto anti-human IgG Fc biosensors for 120 seconds, followed by a 60 second baseline, after which associations were measured by incubating the sensor tip in a dilution series of the trispecific molecules for 180 seconds, followed by dissociation for 300 seconds. Affinities to human serum albumin (HSA) were measured by loading biotinylated albumin onto streptavidin biosensors, then following the same kinetic parameters as for CD3 affinity measurements. All steps were performed at 30.degree. C. in 0.25% casein in phosphate-buffered saline.

[0103] Cytotoxicity Assays

[0104] A human T-cell dependent cellular cytotoxicity (TDCC) assay was used to measure the ability of T cell engagers, including trispecific molecules, to direct T cells to kill tumor cells (Nazarian et al. 2015. J Biomol Screen. 20:519-27). In this assay, T cells and target cancer cell line cells are mixed together at a 10:1 ratio in a 384 wells plate, and varying amounts of T cell engager are added. After 48 hours, the T cells are washed away leaving attached to the plate target cells that were not killed by the T cells. To quantitate the remaining viable cells, CellTiter-Glo.RTM. Luminescent Cell Viability Assay (Promega) is used. In some cases, the target cells are engineered to express luciferase. In these cases, viability of the target cells is assessed by performing a luminescent luciferase assay with STEADYGLO.RTM. reagent (Promega), where viability is directly proportional to the amount of luciferase activity.

[0105] Stability Assays

[0106] The stability of the trispecific binding proteins was assessed at low concentrations in the presence of non-human primate serum. TriTACs were diluted to 33 .mu.g/ml in Cynomolgus serum (BioReclamationIVT) and either incubated for 2 d at 37.degree. C. or subjected to five freeze/thaw cycles. Following the treatment, the samples were assessed in cytotoxicity (TDCC) assays and their remaining activity was compared to untreated stock solutions.

[0107] Xenograft Assays

[0108] The in vivo efficacy of trispecific binding proteins was assessed in xenograft experiments (Crown Bioscience, Taicang). NOD/SCID mice deficient in the common gamma chain (NCG, Model Animal Research Center of Nanjing University) were inoculated on day 0 with a mixture of 5e6 22Rv1 human prostate cancer cells and 5e6 resting, human T cells that were isolated from a healthy, human donor. The mice were randomized into three groups, and treated with vehicle, 0.5 mg/kg PSMA TriTAC C324 or 0.5 mg/kg PSMA BiTE. Treatments were administered daily for 10 days via i.v. bolus injection. Animals were checked daily for morbidity and mortality. Tumor volumes were determined twice weekly with a caliper. The study was terminated after 30 days.

[0109] PK Assays

[0110] The purpose of this study was to evaluate the single dose pharmacokinetics of trispecific binding proteins following intravenous injection. 2 experimentally naive cynomolgus monkeys per group (1 male and 1 female) were given compound via a slow IV bolus injection administered over approximately 1 minute. Following dose administration, cage side observations were performed once daily and body weights were recorded weekly. Blood samples were collected and processed to serum for pharmacokinetic analysis through 21 days post dose administration.

[0111] Concentrations of test articles were determined from monkey serum with an electroluminescent readout (Meso Scale Diagnostics, Rockville). 96 well plates with immobilized, recombinant CD3 were used to capture the analyte. Detection was performed with sulfo-tagged, recombinant PSMA on a MSD reader according to the manufacturer's instructions.

Example 2: Assessing the Impact of CD3 Affinity on the Properties of Trispecific Molecules

[0112] PSMA targeting trispecific molecules with distinct CD3 binding domains were studied to demonstrate the effects of altering CD3 affinity. An exemplary PSMA targeting trispecific molecule is illustrated in FIG. 1. Table 1 lists the affinity of each molecule for the three binding partners (PSMA, CD3, HSA). Affinities were measured by biolayer interferometry using an Octet instrument (Pall Forte Bio). Reduced CD3 affinity leads to a loss in potency in terms of T cell mediated cellular toxicity (FIGS. 2A-C). The pharmacokinetic properties of these trispecific molecules was assessed in cynomolgus monkeys. Molecules with high affinity for CD3 like TriTAC C236 have a terminal half-life of approx. 90 h (FIG. 3). Despite the altered ability to bind CD3 on T cells, the terminal half-life of two molecules with different CD3 affinities shown in FIG. 4 is very similar. However, the reduced CD3 affinity appears to lead to a larger volume of distribution, which is consistent with reduced sequestration of trispecific molecule by T cells. There were no adverse clinical observations or body weight changes noted during the study period.

TABLE-US-00001 TABLE 1 Binding Affinities for Human and Cynomolgus Antigens anti-PSMA KD value (nM) anti-Albumin KD value (nM) anti-CD3e KD value (nM) ratio ratio ratio cyno/ cyno/ cyno/ human cyno hum pHSA CSA hum human cyno hum Tool TriTAC high 16.3 0 0 22.7 25.4 1.1 6.0 4.7 0.8 aff. - C236 TriTAC CD3 high 17.9 0 0 9.8 9.7 1 7.4 5.8 0.8 aff. - C324 TriTAC CD3 med 13.6 0 0 8.8 8.3 0.9 40.6 33.6 0.8 aff. - C339 TriTAC CD3 low 15.3 0 0 10.1 9.7 1 217 160 0.7 aff - C325

Example 3: Assessing the Impact of PSMA Affinity on the Properties of Trispecific Molecules

[0113] PSMA targeting trispecific molecules with distinct PSMA binding domains were studied to demonstrate the effects of altering PSMA affinity. Table 2 lists the affinity of each molecule for the three binding partners (PSMA, CD3, HSA). Reduced PSMA affinity leads to a loss in potency in terms of T cell mediated cellular toxicity (FIGS. 5A-C).

TABLE-US-00002 TABLE 2 Binding Affinities for Human and Cynomolgus Antigens anti-PSMA KD value (nM) anti-Albumin KD value (nM) anti-CD3e KD value (nM) ratio ratio ratio cyno/ cyno/ cyno/ human cyno hum pHSA CSA hum human cyno hum PSMA-TriTAC 22.0 0 n/a 6.6 6.6 1.0 8.3 4.3 0.52 (p8)-C362 PSMA TriTAC 3.7 540 146 7.6 8.4 1.1 8.0 5.2 0.65 (HDS) - C363 PSMA TriTAC 0.15 663 4423 8.4 8.6 1.0 7.7 3.8 0.49 (HTS)- C364

Example 4: In Vivo Efficacy of PSMA Targeting Trispecific Molecules

[0114] The PSMA targeting trispecific molecule C324 was assessed for its ability to inhibit the growth of tumors in mice. For this experiment, immunocompromised mice reconstituted with human T cells were subcutaneously inoculated with PSMA expressing human prostate tumor cells (22Rv1) and treated daily for 10 days with 0.5 mg/kg i.v. of either PSMA targeting BiTE or TriTAC molecules. Tumor growth was measured for 30. Over the course of the experiment, the trispecific molecule was able to inhibit tumor growth with an efficacy comparable to a BiTE molecule (FIG. 6).

Example 5: Specificity of Trispecific Molecules

[0115] In order to assess the specificity of PSMA targeting TriTAC molecules, their ability to induce T cells to kill tumor cells was tested with tumor cells that are negative for PSMA (FIG. 7A). An EGFR targeting TriTAC molecule served as positive control, a GFP targeting TriTAC molecule as negative control. All three TriTACs with distinct PSMA binding domains showed the expected activity against the PSMA positive cell line LNCaP (FIG. 7B), but did not reach EC50s in the PSMA negative tumor cell lines KMS12BM and OVCAR8 (FIGS. 7C and 7D). The EC50s are summarized in Table 3. At very high TriTAC concentrations (>1 nM), some limited off-target cell killing could be observed for TriTACs C362 and C363, while C364 did not show significant cell killing under any of the tested conditions.

TABLE-US-00003 TABLE 3 Cell killing activity of TriTAC molecules in with antigen positive and negative tumor cell lines (EC50 [pM]) TriTAC LNCaP KMS12BM OVCAR8 PSMA p8 TriTAC C362 13.0 >10,000 >10,000 PSMA HDS TriTAC C363 6.2 >10,000 >10,000 PSMA HTS TriTAC C364 0.8 >10,000 >10,000 EGFR TriTAC C131 9.4 >10,000 6 GFP TriTAC C >10,000 >10,000 >10,000

Example 6: Stress Tests and Protein Stability

[0116] Four PSMA targeting trispecific molecules were either incubated for 48 h in Cynomolgus serum at low concentrations (33.3 .mu.g/ml) or subjected to five freeze thaw cycles in Cynomolgus serum. After the treatment, the bio-activity of the TriTAC molecules was assessed in cell killing assays and compared to unstressed samples ("positive control", FIG. 8A-D). All molecules maintained the majority of their cell killing activity. TriTAC C362 was the most stress resistant and did not appear to lose any activity under the conditions tested here.

Example 7: Xenograft Tumor Model

[0117] The PSMA targeting trispecific proteins of the previous examples are evaluated in a xenograft model.

[0118] Male immune-deficient NCG mice are subcutaneously inoculated with 5.times.10.sup.6 22 Rv1 cells into their the right dorsal flank. When tumors reach 100 to 200 mm.sup.3, animals are allocated into 3 treatment groups. Groups 2 and 3 (8 animals each) are intraperitoneally injected with 1.5.times.10.sup.7 activated human T-cells. Three days later, animals from Group 3 are subsequently treated with a total of 9 intravenous doses of 50 .mu.g PSMA trispecific antigen-binding protein of Example 1 (qdx9d). Groups 1 and 2 are only treated with vehicle. Body weight and tumor volume are determined for 30 days. It is expected that tumor growth in mice treated with the PSMA trispecific antigen-binding protein is significantly reduced in comparison to the tumor growth in respective vehicle-treated control group.

Example 8: Proof-of-Concept Clinical Trial Protocol for Administration of the PSMA Trispecific Antigen-Binding Protein of Example 1 to Prostate Cancer Patients

[0119] This is a Phase I/II clinical trial for studying the PSMA trispecific antigen-binding protein of Example 1 as a treatment for Prostate Cancer.

[0120] Study Outcomes:

[0121] Primary: Maximum tolerated dose of PSMA targeting trispecific proteins of the previous examples

[0122] Secondary: To determine whether in vitro response of PSMA targeting trispecific proteins of is the previous examples are associated with clinical response

[0123] Phase I

[0124] The maximum tolerated dose (MTD) will be determined in the phase I section of the trial.

1.1 The maximum tolerated dose (MTD) will be determined in the phase I section of the trial. 1.2 Patients who fulfill eligibility criteria will be entered into the trial to PSMA targeting trispecific proteins of the previous examples. 1.3 The goal is to identify the highest dose of PSMA targeting trispecific proteins of the previous examples that can be administered safely without severe or unmanageable side effects in participants. The dose given will depend on the number of participants who have been enrolled in the study prior and how well the dose was tolerated. Not all participants will receive the same dose.

[0125] Phase II

2.1 A subsequent phase II section will be treated at the MTD with a goal of determining if therapy with therapy of PSMA targeting trispecific proteins of the previous examples results in at least a 20% response rate. Primary Outcome for the Phase II--To determine if therapy of PSMA targeting trispecific proteins of the previous examples results in at least 20% of patients achieving a clinical response (blast response, minor response, partial response, or complete response)

[0126] Eligibility:

[0127] Histologically confirmed newly diagnosed aggressive prostate cancer according to the current World Health Organisation Classification, from 2001 to 2007

[0128] Any stage of disease.

[0129] Treatment with docetaxel and prednisone (+/-surgery).

[0130] Age.gtoreq.18 years

[0131] Karnofsky performance status.gtoreq.50% or ECOG performance status 0-2

[0132] Life expectancy.gtoreq.6 weeks

Example 9: Activity of an Exemplary PSMA Antigen-Binding Protein (PSMA Targeting TriTAC Molecule) in Redirected T Cell Killing Assays Using a Panel of PSMA Expressing Cell Lines and T Cells from Different Donors

[0133] This study was carried out to demonstrate that the activity of the exemplary PSMA trispecific antigen-binding protein is not limited to LNCaP cells or a single cell donor.

[0134] Redirected T cell killing assays were performed using T cells from four different donors and the human PSMA-expressing prostate cancer cell lines VCaP, LNCaP, MDAPCa2b, and 22Rv1. With one exception, the PSMA trispecific antigen-binding protein was able to direct killing of these cancer cell lines using T cells from all donors with EC.sub.50 values of 0.2 to 1.5 pM, as shown in Table 4. With the prostate cancer cell line 22 Rv1 and Donor 24, little to no killing was observed (data not shown). Donor 24 also only resulted approximately 50% killing of the MDAPCa2b cell line whereas T cells from the other 3 donors resulted in almost complete killing of this cell line (data not shown). Control assays demonstrated that killing by the PSMA trispecific antigen-binding protein was PSMA specific. No killing was observed when PSMA-expressing cells were treated with a control trispecific protein targeting green fluorescent protein (GFP) instead of PSMA (data not shown). Similarly, the PSMA trispecific antigen-binding protein was inactive with cell lines that lack PSMA expression, NCI-1563 and HCT116, also shown in Table 4.

TABLE-US-00004 TABLE 4 EC.sub.50 Values from TDCC Assays with Six Human Cancer Cell Lines and Four Different T Cell Donors TDCC EC.sub.50 Values (M) Cell Line Donor 24 Donor 8144 Donor 72 Donor 41 LNCaP 1.5E-12 2.2E-13 3.6E-13 4.3E-13 MDAPCa2b 4.8E-12 4.1E-13 4.9E-13 6.5E-13 VCaP 6.4E-13 1.6E-13 2.0E-13 3.5E-13 22Rv1 n/a 7.2E-13 1.4E-12 1.3E-12 HCT116 >1.0E-8 >1.0E-8 >1.0E-8 >1.0E-8 NCI-1563 >1.0E-8 >1.0E-8 >1.0E-8 >1.0E-8

Example 10: Stimulation of Cytokine Expression in by an Exemplary PSMA Trispecific Antigen-Binding Protein (PSMA Targeting TriTAC Molecule) in Redirected T Cell Killing Assays

[0135] This study was carried out to demonstrate activation of T cells by the exemplary PSMA trispecific antigen-binding protein during redirected T cell killing assays by measuring secretion of cytokine into the assay medium by activated T cells.

[0136] Conditioned media collected from redirected T cell killing assays, as described above in Example 9, were analyzed for expression of the cytokines TNF.alpha. and IFN.gamma.. Cytokines were measured using AlphaLISA assays (Perkin-Elmer). Adding a titration of the PSMA antigen-binding protein to T cells from four different donors and four PSMA-expressing cell lines, LNCaP, VCaP, MDAPCa2b, and 22Rv1 resulted in increased levels of TNF.alpha.. The results for TNF.alpha. expression and IFN .gamma. expression levels in the conditioned media are shown in Tables 5 and 6, respectively. The EC.sub.50 values for the PSMA antigen-binding protein induced expression of these cytokines ranged from 3 to 15 pM. Increased cytokine levels were not observed with a control trispecific protein targeting GFP. Similarly, when assays were performed with two cell lines that lack PSMA expression, HCT116 and NCI-H1563, PSMA HTS TriTAC also did not increase TNF.alpha. or IFN.gamma. expression.

TABLE-US-00005 TABLE 5 EC.sub.50 Values for TNF.alpha. Expression in Media from PSMA Trispecific Antigen-Binding Protein TDCC Assays with Six Human Cancer Cell Lines and T Cells from Four Different Donors Cell Line Donor 24 Donor 8144 Donor 41 Donor72 LNCaP 4.9E-12 2.8E-12 4.0E-12 3.2E-12 VCaP 3.2E-12 2.9E-12 2.9E-12 2.9E-12 MDAPCa2b 2.1E-11 4.0E-12 5.5E-12 3.6E-12 22Rv1 8.9E-12 2.5E-12 4.0E-12 3.3E-12 HCT116 >1E-8 >1E-8 >1E-8 >1E-8 NCI-H1563 >1E-8 >1E-8 >1E-8 >1E-8

TABLE-US-00006 TABLE 6 EC.sub.50 Values for IFN.gamma. Expression in Media from PSMA Trispecific Antigen-Binding Protein TDCC Assays with Six Human Cancer Cell Lines and T Cells from Four Different Donors Cell Line Donor 24 Donor 8144 Donor 41 Donor72 LNCaP 4.2E-12 4.2E-12 4.2E-12 2.8E-12 VCaP 5.1E-12 1.5E-11 3.4E-12 4.9E-12 MDAPCa2b 1.5E-11 5.8E-12 9.7E-12 3.5E-12 22Rv1 7.8E-12 3.0E-12 9.1E-12 3.0E-12 HCT116 >1E-8 >1E-8 >1E-8 >1E-8 NCI-H1563 >1E-8 >1E-8 >1E-8 >1E-8

Example 11: Activity of an Exemplary PSMA Trispecific Antigen-Binding Protein (PSMA Targeting TriTAC) in Redirected T Cell Killing Assay (TDCC) Using T Cells from Cynomolgus Monkeys

[0137] This study was carried out to test the ability of the exemplary PSMA trispecific antigen-binding protein to direct T cells from cynomolgus monkeys to kill PSMA-expressing cell lines.

[0138] TDCC assays were set up using peripheral blood mononuclear cells (PBMCs) from cynomolgus monkeys. Cyno PBMCs were added to LNCaP cells at a 10:1 ratio. It was observed that the PSMA trispecific antigen-binding protein redirected killing of LNCaP by the cyno PBMCs with an EC.sub.50 value of 11 pM. The result is shown in FIG. 9A. To confirm these results, a second cell line was used, MDAPCa2b, and PBMCs from a second cynomolgus monkey donor were tested. Redirected killing of the target cells was observed with an EC.sub.50 value of 2.2 pM. The result is shown in FIG. 9B. Killing was specific to the anti-PMSA arm of the PSMA trispecific antigen-binding protein as killing was not observed with a negative control trispecific protein targeting GFP. These data demonstrate that the PSMA antigen-binding trispecific protein can direct cynomolgus T cells to kill target cells expressing human PSMA.

Example 12: Expression of Markers of T Cell Activation in Redirect T Cell Killing Assays with an Exemplary PSMA Trispecific Antigen-Binding Protein (PSMA Targeting TriTAC Molecule)

[0139] This study was performed to assess whether T cells were activated when the exemplary PSMA trispecific antigen-binding protein directed the T cells to kill target cells.

[0140] The assays were set up using conditions for the redirected T cell killings assays described in the above example. T cell activation was assessed by measuring expression of CD25 and CD69 on the surface of the T cells using flow cytometry. The PSMA trispecific antigen-binding protein was added to a 10:1 mixture of purified human T cells and the prostate cancer cell line VCaP. Upon addition of increasing amounts of the PSMA trispecific antigen-binding protein, increased CD69 expression and CD25 expression was observed, as shown in FIG. 10. EC.sub.50 value was 0.3 pM for CD69 and 0.2 pM for CD25. A trispecific protein targeting GFP was included in these assays as negative control, and little to no increase in CD69 or CD25 expression is observed with the GFP targeting trispecific protein, also shown in FIG. 10.

Example 13: Stimulation of T Cell Proliferation by an Exemplary PSMA Trispecific Antigen-Binding Protein (PSMA Targeting TriTAC Molecule) in the Presence of PSMA Expressing Target Cells

[0141] This study was used as an additional method to demonstrate that the exemplary PSMA trispecific antigen-binding protein was able to activate T cells when it redirects them to kill target cells.

[0142] T cell proliferation assays were set up using the conditions of the T cell redirected killing assay using LNCaP target cells, as described above, and measuring the number of T cells present at 72 hours. The exemplary PSMA trispecific antigen-binding protein stimulated proliferation with an EC.sub.50 value of 0.5 pM. As negative control, a trispecific protein targeting GFP was included in the assay, and no increased proliferation was observed with this protein. The results for the T cell proliferation assay are illustrated in FIG. 11.

Example 14: Redirected T Cell Killing of LNCaP Cells by Three Exemplary PSMA Trispecific Antigen-Binding Proteins (PSMA Targeting TriTAC Molecules PH1T, PH, and Z2)

[0143] This study was carried out to test the ability of three exemplary PSMA trispecific antigen-binding proteins, having the sequences as set forth in SEQ ID Nos: 150, 151, and 152, to redirect T cells to kill the LNCaP cell line.

[0144] In TDCC assays, set up as described in above examples, the PSMA PH1T TriTAC (SEQ ID No: 150) and PSMA PH1 TriTAC (SEQ ID NO: 151) proteins directed killing with EC.sub.50 values of 25 and 20 pM, respectively, as shown in FIG. 12A; and the PSMA Z2 TriTAC (SEQ ID NO: 152) protein directed killing with an EC.sub.50 value of 0.8 pM, as shown in FIG. 12B.

TABLE-US-00007 TABLE 7 CD3 Binding Domain Sequences SEQ ID NO: Description AA Sequence 1 Anti-CD3, clone 2B2 EVQLVESGGGLVQPGGSLKLSCAASGFTFNKYAINWVRQAPGKGL EWVARIRSKYNNYATYYADQVKDRFTISRDDSKNTAYLQMNNLKT EDTAVYYCVRHANFGNSYISYWAYWGQGTLVTVSSGGGGSGGGG SGGGGSQTVVTQEPSLTVSPGGTVTLTCASSTGAVTSGNYPNWVQQ KPGQAPRGLIGGTKFLVPGTPARFSGSLLGGKAALTLSGVQPEDEAE YYCTLWYSNRWVFGGGTKLTVL 2 Anti-CD3, clone 9F2 EVQLVESGGGLVQPGGSLKLSCAASGFEFNKYAMNWVRQAPGKG LEWVARIRSKYNKYATYYADSVKDRFTISRDDSKNTAYLQMNNLK TEDTAVYYCVRHGNFGNSYISYWAYWGQGTLVTVSSGGGGSGGG GSGGGGSQTVVTQEPSLTVSPGGTVTLTCGSSFGAVTSGNYPNWVQ QKPGQAPRGLIGGTKFLAPGTPARFSGSLLGGKAALTLSGVQPEDE AEYYCVLWYDNRWVFGGGTKLTVL 3 Anti-CD3, clone 5A2 EVQLVESGGGLVQPGGSLKLSCAASGFTFNKYAMNWVRQAPGKG LEWVARIRSKYNNYATYYADSVKDRFTISRDDSKNTAYLQMNNLK TEDTAVYYCVRHGNFGNSHISYWAYWGQGTLVTVSSGGGGSGGG GSGGGGSQTVVTQEPSLTVSPGGTVTLTCGSSTGYVTSGNYPNWVQ QKPGQAPRGLIGGTSFLAPGTPARFSGSLLGGKAALTLSGVQPEDEA EYYCVLWYSNRWIFGGGTKLTVL 4 Anti-CD3, clone 6A2 EVQLVESGGGLVQPGGSLKLSCAASGFMFNKYAMNWVRQAPGKG LEWVARIRSKSNNYATYYADSVKDRFTISRDDSKNTAYLQMNNLK TEDTAVYYCVRHGNFGNSYISYWATWGQGTLVTVSSGGGGSGGG GSGGGGSQTVVTQEPSLTVSPGGTVTLTCGSSFGAVTSGNYPNWVQ QKPGQAPRGLIGGTKLLAPGTPARFSGSLLGGKAALTLSGVQPEDE AEYYCVLWYSNSWVFGGGTKLTVL 5 Anti-CD3, clone 2D2 EVQLVESGGGLVQPGGSLKLSCAASGFTFNTYAMNWVRQAPGKGL EWVARIRSKYNNYATYYKDSVKDRFTISRDDSKNTAYLQMNNLKT EDTAVYYCVRHGNFGNSPISYWAYWGQGTLVTVSSGGGGSGGGG SGGGGSQTVVTQEPSLTVSPGGTVTLTCGSSTGAVVSGNYPNWVQ QKPGQAPRGLIGGTEFLAPGTPARFSGSLLGGKAALTLSGVQPEDEA EYYCVLWYSNRWVFGGGTKLTVL 6 Anti-CD3, clone 3F2 EVQLVESGGGLVQPGGSLKLSCAASGFTYNKYAMNWVRQAPGKG LEWVARIRSKYNNYATYYADEVKDRFTISRDDSKNTAYLQMNNLK TEDTAVYYCVRHGNFGNSPISYWAYWGQGTLVTVSSGGGGSGGG GSGGGGSQTVVTQEPSLTVSPGGTVTLTCGSSKGAVTSGNYPNWV QQKPGQAPRGLIGGTKELAPGTPARFSGSLLGGKAALTLSGVQPED EAEYYCTLWYSNRWVFGGGTKLTVL 7 Anti-CD3, clone 1A2 EVQLVESGGGLVQPGGSLKLSCAASGNTFNKYAMNWVRQAPGKG LEWVARIRSKYNNYETYYADSVKDRFTISRDDSKNTAYLQMNNLK TEDTAVYYCVRHTNFGNSYISYWAYWGQGTLVTVSSGGGGSGGG GSGGGGSQTVVTQEPSLTVSPGGTVTLTCGSSTGAVTSGYYPNWVQ QKPGQAPRGLIGGTYFLAPGTPARFSGSLLGGKAALTLSGVQPEDE AEYYCVLWYSNRWVFGGGTKLTVL 8 Anti-CD3, clone 1C2 EVQLVESGGGLVQPGGSLKLSCAASGFTFNNYAMNWVRQAPGKG LEWVARIRSKYNNYATYYADAVKDRFTISRDDSKNTAYLQMNNLK TEDTAVYYCVRHGNFGNSQISYWAYWGQGTLVTVSSGGGGSGGG GSGGGGSQTVVTQEPSLTVSPGGTVTLTCGSSTGAVTDGNYPNWV QQKPGQAPRGLIGGIKFLAPGTPARFSGSLLGGKAALTLSGVQPEDE AEYYCVLWYSNRWVFGGGTKLTVL 9 Anti-CD3, clone 2E4 EVQLVESGGGLVQPGGSLKLSCAASGFTFNKYAVNWVRQAPGKGL EWVARIRSKYNNYATYYADSVKDRFTISRDDSKNTAYLQMNNLKT EDTAVYYCVRHGNFGNSYISYWAYWGQGTLVTVSSGGGGSGGGG SGGGGSQTVVTQEPSLTVSPGGTVTLTCGESTGAVTSGNYPNWVQ QKPGQAPRGLIGGTKILAPGTPARFSGSLLGGKAALTLSGVQPEDEA EYYCVLWYSNRWVFGGGTKLTVL 10 Anti-CD3, clone 10E4 EVQLVESGGGLVQPGGSLKLSCAASGFTFNKYPMNWVRQAPGKGL EWVARIRSKYNNYATYYADSVKDRFTISRDDSKNTAYLQMNNLKN EDTAVYYCVRHGNFNNSYISYWAYWGQGTLVTVSSGGGGSGGGG SGGGGSQTVVTQEPSLTVSPGGTVTLTCGSSTGAVTKGNYPNWVQ QKPGQAPRGLIGGTKMLAPGTPARFSGSLLGGKAALTLSGVQPEDE AEYYCALWYSNRWVFGGGTKLTVL 11 Anti-CD3, clone 2H2 EVQLVESGGGLVQPGGSLKLSCAASGFTFNGYAMNWVRQAPGKG LEWVARIRSKYNNYATYYADEVKDRFTISRDDSKNTAYLQMNNLK TEDTAVYYCVRHGNFGNSPISYWAYWGQGTLVTVSSGGGGSGGG GSGGGGSQTVVTQEPSLTVSPGGTVTLTCGSSTGAVVSGNYPNWV QQKPGQAPRGLIGGTEFLAPGTPARFSGSLLGGKAALTLSGVQPEDE AEYYCVLWYSNRWVFGGGTKLTVL 12 Anti-CD3, clone 2A4 EVQLVESGGGLVQPGGSLKLSCAASGNTFNKYAMNWVRQAPGKG LEWVARIRSKYNNYATYYADSVKDRFTISRDDSKNTAYLQMNNLK TEDTAVYYCVRHGNFGDSYISYWAYWGQGTLVTVSSGGGGSGGG GSGGGGSQTVVTQEPSLTVSPGGTVTLTCGSSTGAVTHGNYPNWV QQKPGQAPRGLIGGTKVLAPGTPARFSGSLLGGKAALTLSGVQPED EAEYYCVLWYSNRWVFGGGTKLTVL 13 Anti-CD3, clone 10B2 EVQLVESGGGLVQPGGSLKLSCAASGFTFNNYAMNWVRQAPGKG LEWVARIRSGYNNYATYYADSVKDRFTISRDDSKNTAYLQMNNLK TEDTAVYYCVRHGNFGNSYISYWAYWGQGTLVTVSSGGGGSGGG GSGGGGSQTVVTQEPSLTVSPGGTVTLTCGSYTGAVTSGNYPNWV QQKPGQAPRGLIGGTKFNAPGTPARFSGSLLGGKAALTLSGVQPED EAEYYCVLWYANRWVFGGGTKLTVL 14 Anti-CD3, clone 1G4 EVQLVESGGGLVQPGGSLKLSCAASGFEFNKYAMNWVRQAPGKG LEWVARIRSKYNNYETYYADSVKDRFTISRDDSKNTAYLQMNNLK TEDTAVYYCVRHGNFGNSLISYWAYWGQGTLVTVSSGGGGSGGG GSGGGGSQTVVTQEPSLTVSPGGTVTLTCGSSSGAVTSGNYPNWVQ QKPGQAPRGLIGGTKFGAPGTPARFSGSLLGGKAALTLSGVQPEDE AEYYCVLWYSNRWVFGGGTKLTVL 15 wt anti-CD3 EVQLVESGGGLVQPGGSLKLSCAASGFTFNKYAMNWVRQAPGKG LEWVARIRSKYNNYATYYADSVKDRFTISRDDSKNTAYLQMNNLK TEDTAVYYCVRHGNFGNSYISYWAYWGQGTLVTVSSGGGGSGGG GSGGGGSQTVVTQEPSLTVSPGGTVTLTCGSSTGAVTSGNYPNWVQ QKPGQAPRGLIGGTKFLAPGTPARFSGSLLGGKAALTLSGVQPEDE AEYYCVLWYSNRWVFGGGTKLTVL 16 wt anti-CD3 HC CDR1 GFTFNKYAMN 17 wt anti-CD3 HC CDR2 RIRSKYNNYATYYADSVK 18 wt anti-CD3 HC CDR3 HGNFGNSYISYWAY 19 wt anti-CD3 LC CDR1 GSSTGAVTSGNYPN 20 wt anti-CD3 LC CDR2 GTKFLAP 21 wt anti-CD3 LC CDR3 VLWYSNRWV 22 HC CDR1 variant 1 GNTFNKYAMN 23 HC CDR1 variant 2 GFEFNKYAMN 24 HC CDR1 variant 3 GFMFNKYAMN 25 HC CDR1 variant 4 GFTYNKYAMN 26 HC CDR1 variant 5 GFTFNNYAMN 27 HC CDR1 variant 6 GFTFNGYAMN 28 HC CDR1 variant 7 GFTFNTYAMN 29 HC CDR1 variant 8 GFTFNEYAMN 30 HC CDR1 variant 9 GFTFNKYPMN 31 HC CDR1 variant 10 GFTFNKYAVN 32 HC CDR1 variant 11 GFTFNKYAIN 33 HC CDR1 variant 12 GFTFNKYALN 34 HC CDR2 variant 1 RIRSGYNNYATYYADSVK 35 HC CDR2 variant 2 RIRSKSNNYATYYADSVK 36 HC CDR2 variant 3 RIRSKYNKYATYYADSVK 37 HC CDR2 variant 4 RIRSKYNNYETYYADSVK 38 HC CDR2 variant 5 RIRSKYNNYATEYADSVK 39 HC CDR2 variant 6 RIRSKYNNYATYYKDSVK 40 HC CDR2 variant 7 RIRSKYNNYATYYADEVK 41 HC CDR2 variant 8 RIRSKYNNYATYYADAVK 42 HC CDR2 variant 9 RIRSKYNNYATYYADQVK 43 HC CDR2 variant 10 RIRSKYNNYATYYADDVK 44 HC CDR3 variant 1 HANFGNSYISYWAY 45 HC CDR3 variant 2 HTNFGNSYISYWAY 46 HC CDR3 variant 3 HGNFNNSYISYWAY 47 HC CDR3 variant 4 HGNFGDSYISYWAY 48 HC CDR3 variant 5 HGNFGNSHISYWAY 49 HC CDR3 variant 6 HGNFGNSPISYWAY 50 HC CDR3 variant 7 HGNFGNSQISYWAY 51 HC CDR3 variant 8 HGNFGNSLISYWAY 52 HC CDR3 variant 9 HGNFGNSGISYWAY 53 HC CDR3 variant 10 HGNFGNSYISYWAT 54 LC CDR1 variant 1 ASSTGAVTSGNYPN 55 LC CDR1 variant 2 GESTGAVTSGNYPN 56 LC CDR1 variant 3 GSYTGAVTSGNYPN 57 LC CDR1 variant 4 GSSFGAVTSGNYPN 58 LC CDR1 variant 5 GSSKGAVTSGNYPN 59 LC CDR1 variant 6 GSSSGAVTSGNYPN 60 LC CDR1 variant 7 GSSTGYVTSGNYPN 61 LC CDR1 variant 8 GSSTGAVVSGNYPN 62 LC CDR1 variant 9 GSSTGAVTDGNYPN 63 LC CDR1 variant 10 GSSTGAVTKGNYPN 64 LC CDR1 variant 11 GSSTGAVTHGNYPN 65 LC CDR1 variant 12 GSSTGAVTVGNYPN 66 LC CDR1 variant 13 GSSTGAVTSGYYPN 67 LC CDR2 variant 1 GIKFLAP 68 LC CDR2 variant 2 GTEFLAP 69 LC CDR2 variant 3 GTYFLAP 70 LC CDR2 variant 4 GTSFLAP 71 LC CDR2 variant 5 GTNFLAP 72 LC CDR2 variant 6 GTKLLAP 73 LC CDR2 variant 7 GTKELAP 74 LC CDR2 variant 8 GTKILAP 75 LC CDR2 variant 9 GTKMLAP 76 LC CDR2 variant 10 GTKVLAP 77 LC CDR2 variant 11 GTKFNAP 78 LC CDR2 variant 12 GTKFGAP 79 LC CDR2 variant 13 GTKFLVP 80 LC CDR3 variant 1 TLWYSNRWV 81 LC CDR3 variant 2 ALWYSNRWV 82 LC CDR3 variant 3 VLWYDNRWV 83 LC CDR3 variant 4 VLWYANRWV 84 LC CDR3 variant 5 VLWYSNSWV

85 LC CDR3 variant 6 VLWYSNRWI 86 LC CDR3 variant 7 VLWYSNRWA 87 Anti-CD3, clone 2G5 EVQLVESGGGLVQPGGSLKLSCAASGFTFNKYALNWVRQAPGKGL EWVARIRSKYNNYATEYADSVKDRFTISRDDSKNTAYLQMNNLKT EDTAVYYCVRHGNFGNSPISYWAYWGQGTLVTVSSGGGGSGGGG SGGGGSQTVVTQEPSLTVSPGGTVTLTCGSSTGAVTSGNYPNWVQQ KPGQAPRGLIGGTNFLAPGTPERFSGSLLGGKAALTLSGVQPEDEAE YYCVLWYSNRWAFGGGTKLTVL 88 Anti-CD3, clone 8A5 EVQLVESGGGLVQPGGSLKLSCAASGFTFNEYAMNWVRQAPGKGL EWVARIRSKYNNYATYYADDVKDRFTISRDDSKNTAYLQMNNLKT EDTAVYYCVRHGNFGNSGISYWAYWGQGTLVTVSSGGGGSGGGG SGGGGSQTVVTQEPSLTVSPGGTVTLTCGSSTGAVTVGNYPNWVQ QKPGQAPRGLIGGTEFLAPGTPARFSGSLLGGKAALTLSGVQPEDEA EYYCVLWYSNRWVFGGGTKLTVL

TABLE-US-00008 TABLE 8 HSA Binding Domain Sequences SEQ ID NO: Description AA Sequence 89 Anti-HSA sdAb clone 6C EVQLVESGGGLVQPGNSLRLSCAASGFTFSRFGMSWVRQAPGKGL EWVSSISGSGSDTLYADSVKGRFTISRDNAKTTLYLQMNSLRPEDTA VYYCTIGGSLSRSSQGTLVTVSS 90 Anti-HSA sdAb clone 7A EVQLVESGGGLVQPGNSLRLSCAASGFTFSKFGMSWVRQAPGKGL EWVSSISGSGADTLYADSLKGRFTISRDNAKTTLYLQMNSLRPEDT AVYYCTIGGSLSKSSQGTLVTVSS 91 Anti-HSA sdAb clone 7G EVQLVESGGGLVQPGNSLRLSCAASGFTYSSFGMSWVRQAPGKGL EWVSSISGSGSDTLYADSVKGRFTISRDNAKTTLYLQMNSLRPEDTA VYYCTIGGSLSKSSQGTLVTVSS 92 Anti-HSA sdAb clone 8H EVQLVESGGGLVQPGNSLRLSCAASGFTFSKFGMSWVRQAPGKGL EWVSSISGSGTDTLYADSVKGRFTISRDNAKTTLYLQMNSLRPEDT AVYYCTIGGSLSRSSQGTLVTVSS 93 Anti-HSA sdAb clone 9A EVQLVESGGGLVQPGNSLRLSCAASGFTFSRFGMSWVRQAPGKGL EWVSSISGSGSDTLYADSVKGRFTISRDNAKTTLYLQMNSLRPEDTA VYYCTIGGSLSKSSQGTLVTVSS 94 Anti-HSA sdAb clone 10G EVQLVESGGGLVQPGNSLRLSCAASGFTFSKFGMSWVRQAPGKGL EWVSSISGSGRDTLYADSVKGRFTISRDNAKTTLYLQMNSLRPEDT AVYYCTIGGSLSVSSQGTLVTVSS 95 wt anti-HSA EVQLVESGGGLVQPGNSLRLSCAASGFTFSSFGMSWVRQAPGKGLE WVSSISGSGSDTLYADSVKGRFTISRDNAKTTLYLQMNSLRPEDTA VYYCTIGGSLSRSSQGTLVTVSS 96 wt anti-HSA CDR1 GFTFSSFGMS 97 wt anti-HSA CDR2 SISGSGSDTLYADSVK 98 wt anti-HSACDR3 GGSLSR 99 CDR1 variant 1 GFTFSRFGMS 100 CDR1 variant 2 GFTFSKFGMS 101 CDR1 variant 3 GFTYSSFGMS 102 CDR2 variant 1 SISGSGADTLYADSLK 103 CDR2 variant 2 SISGSGTDTLYADSVK 104 CDR2 variant 3 SISGSGRDTLYADSVK 105 CDR2 variant 4 SISGSGSDTLYAESVK 106 CDR2 variant 5 SISGSGTDTLYAESVK 107 CDR2 variant 6 SISGSGRDTLYAESVK 108 CDR3 variant 1 GGSLSK 109 CDR3 variant 2 GGSLSV 110 Anti-HSA sdAb clone 6CE EVQLVESGGGLVQPGNSLRLSCAASGFTFSRFGMSWVRQAPGKGL EWVSSISGSGSDTLYAESVKGRFTISRDNAKTTLYLQMNSLRPEDTA VYYCTIGGSLSRSSQGTLVTVSS 111 Anti-HSA sdAb clone 8HE EVQLVESGGGLVQPGNSLRLSCAASGFTFSKFGMSWVRQAPGKGL EWVSSISGSGTDTLYAESVKGRFTISRDNAKTTLYLQMNSLRPEDTA VYYCTIGGSLSRSSQGTLVTVSS 112 Anti-HSA sdAb clone 10GE EVQLVESGGGLVQPGNSLRLSCAASGFTFSKFGMSWVRQAPGKGL EWVSSISGSGRDTLYAESVKGRFTISRDNAKTTLYLQMNSLRPEDTA VYYCTIGGSLSVSSQGTLVTVSS

TABLE-US-00009 TABLE 9 PSMA Binding Domain Sequences SEQ ID NO: Description AA Sequence 113 wt anti-PSMA EVQLVESGGGLVQPGGSLTLSCAASRFMISEYSMHWVRQAPGKGL EWVSTINPAGTTDYAESVKGRFTISRDNAKNTLYLQMNSLKPEDTA VYYCDGYGYRGQGTQVTVSS 114 CDR1 variant 1 RFMISEYHMH 115 CDR1 variant 2 RFMISPYSMH 116 CDR1 variant 3 RFMISPYHMH 117 CDR2 variant 1 DINPAGTTDYAESVKG 118 CDR2 variant 2 TINPAKTTDYAESVKG 119 CDR2 variant 3 TINPAGQTDYAESVKG 120 CDR2 variant 4 TINPAGTTDYAEYVKG 121 CDR2 variant 5 DINPAKTTDYAESVKG 122 CDR2 variant 6 DINPAGQTDYAESVKG 123 CDR2 variant 7 DINPAGTTDYAEYVKG 124 CDR3 variant 1 DSYGY 125 CDR1 variant 4 RFMISEYSMH 126 CDR2 variant 8 TINPAGTTDYAESVKG 127 CDR3 variant 2 DGYGY 128 Anti-PSMA clone 1 EVQLVESGGGLVQPGGSLRLSCAASRFMISEYSMHWVRQAPGKGL EWVSTINPAGTTDYAESVKGRFTISRDNAKNTLYLQMNSLRAEDTA VYYCDGYGYRGQGTLVTVSS 129 Anti-PSMA clone 2 EVQLVESGGGLVQPGGSLRLSCAASRFMISEYHMHWVRQAPGKGL EWVSDINPAGTTDYAESVKGRFTISRDNAKNTLYLQMNSLRAEDTA VYYCDSYGYRGQGTLVTVSS 130 Anti-PSMA clone 3 EVQLVESGGGLVQPGGSLRLSCAASRFMISEYHMHWVRQAPGKGL EWVSTINPAGTTDYAESVKGRFTISRDNAKNTLYLQMNSLRAEDTA VYYCDSYGYRGQGTLVTVSS 131 Anti-PSMA clone 4 EVQLVESGGGLVQPGGSLRLSCAASRFMISEYSMHWVRQAPGKGL EWVSTINPAKTTDYAESVKGRFTISRDNAKNTLYLQMNSLRAEDTA VYYCDSYGYRGQGTLVTVSS 132 Anti-PSMA clone 5 EVQLVESGGGLVQPGGSLRLSCAASRFMISPYSMHWVRQAPGKGL EWVSTINPAGTTDYAESVKGRFTISRDNAKNTLYLQMNSLRAEDTA VYYCDGYGYRGQGTLVTVSS 133 Anti-PSMA clone 6 EVQLVESGGGLVQPGGSLRLSCAASRFMISEYSMHWVRQAPGKGL EWVSTINPAGQTDYAESVKGRFTISRDNAKNTLYLQMNSLRAEDTA VYYCDGYGYRGQGTLVTVSS 134 Anti-PSMA clone 7 EVQLVESGGGLVQPGGSLRLSCAASRFMISEYSMHWVRQAPGKGL EWVSTINPAGTTDYAEYVKGRFTISRDNAKNTLYLQMNSLRAEDTA VYYCDGYGYRGQGTLVTVSS 135 Anti-PSMA clone 8 EVQLVESGGGLVQPGGSLRLSCAASRFMISEYHMHWVRQAPGKGL EWVSDINPAKTTDYAESVKGRFTISRDNAKNTLYLQMNSLRAEDTA VYYCDSYGYRGQGTLVTVSS 136 Anti-PSMA clone 9 EVQLVESGGGLVQPGGSLRLSCAASRFMISPYHMHWVRQAPGKGL EWVSDINPAGTTDYAESVKGRFTISRDNAKNTLYLQMNSLRAEDTA VYYCDSYGYRGQGTLVTVSS 137 Anti-PSMA clone 10 EVQLVESGGGLVQPGGSLRLSCAASRFMISEYHMHWVRQAPGKGL EWVSDINPAGQTDYAESVKGRFTISRDNAKNTLYLQMNSLRAEDT AVYYCDSYGYRGQGTLVTVSS 138 Anti-PSMA clone 11 EVQLVESGGGLVQPGGSLRLSCAASRFMISEYHMHWVRQAPGKGL EWVSDINPAGTTDYAEYVKGRFTISRDNAKNTLYLQMNSLRAEDT AVYYCDSYGYRGQGTLVTVSS 139 Anti-PSMA clone 12 EVQLVESGGGLVQPGGSLTLSCAASRFMISEYHMHWVRQAPGKGL EWVSDINPAGTTDYAESVKGRFTISRDNAKNTLYLQMNSLKPEDTA VYYCDSYGYRGQGTQVTVSS 140 Anti-PSMA clone 13 EVQLVESGGGLVQPGGSLTLSCAASRFMISEYHMHWVRQAPGKGL EWVSTINPAGTTDYAESVKGRFTISRDNAKNTLYLQMNSLKPEDTA VYYCDSYGYRGQGTQVTVSS

TABLE-US-00010 TABLE 10 PSMA Targeting Trispecific Protein Sequences SEQ ID C- NO: Number Construct Sequence 141 C00324 PSMA EVQLVESGGGLVQPGGSLTLSCAASRFMISEYSMHWVRQAPGK TriTAC CD3 GLEWVSTINPAGTTDYAESVKGRFTISRDNAKNTLYLQMNSLKP high aff. EDTAVYYCDGYGYRGQGTQVTVSSGGGGSGGGSEVQLVESGG GLVQPGNSLRLSCAASGFTFSKFGMSWVRQAPGKGLEWVSSISG SGRDTLYADSVKGRFTISRDNAKTTLYLQMNSLRPEDTAVYYCT IGGSLSVSSQGTLVTVSSGGGGSGGGSEVQLVESGGGLVQPGGS LKLSCAASGFTFNKYAINWVRQAPGKGLEWVARIRSKYNNYAT YYADQVKDRFTISRDDSKNTAYLQMNNLKTEDTAVYYCVRHA NFGNSYISYWAYWGQGTLVTVSSGGGGSGGGGSGGGGSQTVV TQEPSLTVSPGGTVTLTCASSTGAVTSGNYPNWVQQKPGQAPRG LIGGTKFLVPGTPARFSGSLLGGKAALTLSGVQPEDEAEYYCTL WYSNRWVFGGGTKLTVLHHHHHH 142 C00339 PSMA EVQLVESGGGLVQPGGSLTLSCAASRFMISEYSMHWVRQAPGK TriTAC CD3 GLEWVSTINPAGTTDYAESVKGRFTISRDNAKNTLYLQMNSLKP med. aff. EDTAVYYCDGYGYRGQGTQVTVSSGGGGSGGGSEVQLVESGG GLVQPGNSLRLSCAASGFTFSKFGMSWVRQAPGKGLEWVSSISG SGRDTLYADSVKGRFTISRDNAKTTLYLQMNSLRPEDTAVYYCT IGGSLSVSSQGTLVTVSSGGGGSGGGSEVQLVESGGGLVQPGGS LKLSCAASGFTFNNYAMNWVRQAPGKGLEWVARIRSGYNNYA TYYADSVKDRFTISRDDSKNTAYLQMNNLKTEDTAVYYCVRHG NFGNSYISYWAYWGQGTLVTVSSGGGGSGGGGSGGGGSQTVV TQEPSLTVSPGGTVTLTCGSYTGAVTSGNYPNWVQQKPGQAPR GLIGGTKFNAPGTPARFSGSLLGGKAALTLSGVQPEDEAEYYCV LWYANRWVFGGGTKLTVLHHHHHH 143 C00325 PSMA EVQLVESGGGLVQPGGSLTLSCAASRFMISEYSMHWVRQAPGK TriTAC CD3 GLEWVSTINPAGTTDYAESVKGRFTISRDNAKNTLYLQMNSLKP low aff. EDTAVYYCDGYGYRGQGTQVTVSSGGGGSGGGSEVQLVESGG GLVQPGNSLRLSCAASGFTFSKFGMSWVRQAPGKGLEWVSSISG SGRDTLYADSVKGRFTISRDNAKTTLYLQMNSLRPEDTAVYYCT IGGSLSVSSQGTLVTVSSGGGGSGGGSEVQLVESGGGLVQPGGS LKLSCAASGFEFNKYAMNWVRQAPGKGLEWVARIRSKYNNYE TYYADSVKDRFTISRDDSKNTAYLQMNNLKTEDTAVYYCVRHG NFGNSLISYWAYWGQGTLVTVSSGGGGSGGGGSGGGGSQTVVT QEPSLTVSPGGTVTLTCGSSSGAVTSGNYPNWVQQKPGQAPRGL IGGTKFGAPGTPARFSGSLLGGKAALTLSGVQPEDEAEYYCVLW YSNRWVFGGGTKLTVLHHHHHH 144 C00236 Tool PSMA EVQLVESGGGLVQPGGSLTLSCAASRFMISEYSMHWVRQAPGK TriTAC GLEWVSTINPAGTTDYAESVKGRFTISRDNAKNTLYLQMNSLKP EDTAVYYCDGYGYRGQGTQVTVSSGGGGSGGGSEVQLVESGG GLVQPGNSLRLSCAASGFTFSSFGMSWVRQAPGKGLEWVSSISG SGSDTLYADSVKGRFTISRDNAKTTLYLQMNSLRPEDTAVYYCT IGGSLSRSSQGTLVTVSSGGGGSGGGSEVQLVESGGGLVQPGGS LKLSCAASGFTFNKYAMNWVRQAPGKGLEWVARIRSKYNNYA TYYADSVKDRFTISRDDSKNTAYLQMNNLKTEDTAVYYCVRHG NFGNSYISYWAYWGQGTLVTVSSGGGGSGGGGSGGGGSQTVV TQEPSLTVSPGGTVTLTCGSSTGAVTSGNYPNWVQQKPGQAPRG LIGGTKFLAPGTPARFSGSLLGGKAALTLSGVQPEDEAEYYCVL WYSNRWVFGGGTKLTVLHHHHHH 145 C00362 PSMA p8 EVQLVESGGGLVQPGGSLRLSCAASRFMISEYSMHWVRQAPGK TriTAC GLEWVSTINPAGTTDYAESVKGRFTISRDNAKNTLYLQMNSLRA EDTAVYYCDGYGYRGQGTLVTVSSGGGGSGGGSEVQLVESGG GLVQPGNSLRLSCAASGFTFSKFGMSWVRQAPGKGLEWVSSISG SGRDTLYADSVKGRFTISRDNAKTTLYLQMNSLRPEDTAVYYCT IGGSLSVSSQGTLVTVSSGGGGSGGGSEVQLVESGGGLVQPGGS LKLSCAASGFTFNKYAINWVRQAPGKGLEWVARIRSKYNNYAT YYADQVKDRFTISRDDSKNTAYLQMNNLKTEDTAVYYCVRHA NFGNSYISYWAYWGQGTLVTVSSGGGGSGGGGSGGGGSQTVV TQEPSLTVSPGGTVTLTCASSTGAVTSGNYPNWVQQKPGQAPRG LIGGTKFLVPGTPARFSGSLLGGKAALTLSGVQPEDEAEYYCTL WYSNRWVFGGGTKLTVLHHHHHH 146 C00363 PSMA HDS EVQLVESGGGLVQPGGSLTLSCAASRFMISEYHMHWVRQAPGK TriTAC GLEWVSDINPAGTTDYAESVKGRFTISRDNAKNTLYLQMNSLKP C363 EDTAVYYCDSYGYRGQGTQVTVSSGGGGSGGGSEVQLVESGGG LVQPGNSLRLSCAASGFTFSKFGMSWVRQAPGKGLEWVSSISGS GRDTLYADSVKGRFTISRDNAKTTLYLQMNSLRPEDTAVYYCTI GGSLSVSSQGTLVTVSSGGGGSGGGSEVQLVESGGGLVQPGGSL KLSCAASGFTFNKYAINWVRQAPGKGLEWVARIRSKYNNYATY YADQVKDRFTISRDDSKNTAYLQMNNLKTEDTAVYYCVRHANF GNSYISYWAYWGQGTLVTVSSGGGGSGGGGSGGGGSQTVVTQ EPSLTVSPGGTVTLTCASSTGAVTSGNYPNWVQQKPGQAPRGLI GGTKFLVPGTPARFSGSLLGGKAALTLSGVQPEDEAEYYCTLWY SNRWVFGGGTKLTVLHHHHHH 147 C00364 PSMA HTS EVQLVESGGGLVQPGGSLTLSCAASRFMISEYHMHWVRQAPGK TriTAC GLEWVSTINPAGTTDYAESVKGRFTISRDNAKNTLYLQMNSLKP C364 EDTAVYYCDSYGYRGQGTQVTVSSGGGGSGGGSEVQLVESGGG LVQPGNSLRLSCAASGFTFSKFGMSWVRQAPGKGLEWVSSISGS GRDTLYADSVKGRFTISRDNAKTTLYLQMNSLRPEDTAVYYCTI GGSLSVSSQGTLVTVSSGGGGSGGGSEVQLVESGGGLVQPGGSL KLSCAASGFTFNKYAINWVRQAPGKGLEWVARIRSKYNNYATY YADQVKDRFTISRDDSKNTAYLQMNNLKTEDTAVYYCVRHANF GNSYISYWAYWGQGTLVTVSSGGGGSGGGGSGGGGSQTVVTQ EPSLTVSPGGTVTLTCASSTGAVTSGNYPNWVQQKPGQAPRGLI GGTKFLVPGTPARFSGSLLGGKAALTLSGVQPEDEAEYYCTLWY SNRWVFGGGTKLTVLHHHHHH 148 C00298 PSMA BiTE QVQLVESGGGLVKPGESLRLSCAASGFTFSDYYMYWVRQAPGK GLEWVAIISDGGYYTYYSDIIKGRFTISRDNAKNSLYLQMNSLKA EDTAVYYCARGFPLLRHGAMDYWGQGTLVTVSSGGGGSGGGG SGGGGSDIQMTQSPSSLSASVGDRVTITCKASQNVDTNVAWYQ QKPGQAPKSLIYSASYRYSDVPSRFSGSASGTDFTLTISSVQSEDF ATYYCQQYDSYPYTFGGGTKLEIKSGGGGSEVQLVESGGGLVQP GGSLKLSCAASGFTFNKYAMNWVRQAPGKGLEWVARIRSKYN NYATYYADSVKDRFTISRDDSKNTAYLQMNNLKTEDTAVYYCV RHGNFGNSYISYWAYWGQGTLVTVSSGGGGSGGGGSGGGGSQ TVVTQEPSLTVSPGGTVTLTCGSSTGAVTSGNYPNWVQQKPGQ APRGLIGGTKFLAPGTPARFSGSLLGGKAALTLSGVQPEDEAEYY CVLWYSNRWVFGGGTKLTVLHHHHHH 149 C00131 EGFR QVKLEESGGGSVQTGGSLRLTCAASGRTSRSYGMGWFRQAPGK TriTAC EREFVSGISWRGDSTGYADSVKGRFTISRDNAKNTVDLQMNSLK PEDTAIYYCAAAAGSAWYGTLYEYDYWGQGTQVTVSSGGGGS GGGSEVQLVESGGGLVQPGNSLRLSCAASGFTFSSFGMSWVRQ APGKGLEWVSSISGSGSDTLYADSVKGRFTISRDNAKTTLYLQM NSLRPEDTAVYYCTIGGSLSRSSQGTLVTVSSGGGGSGGGSEVQL VESGGGLVQPGGSLKLSCAASGFTFNKYAMNWVRQAPGKGLE WVARIRSKYNNYATYYADSVKDRFTISRDDSKNTAYLQMNNLK TEDTAVYYCVRHGNFGNSYISYWAYWGQGTLVTVSSGGGGSG GGGSGGGGSQTVVTQEPSLTVSPGGTVTLTCGSSTGAVTSGNYP NWVQQKPGQAPRGLIGGTKFLAPGTPARFSGSLLGGKAALTLSG VQPEDEAEYYCVLWYSNRWVFGGGTKLTVLHHHHHH 150 C00457 PSMA PH1T QVQLVESGGGVVQAGRSLTLSCAYSGVTVNVYRMGWFRQAPG TriTAC KEREFVANINWSGNNRDYADSVRGRFTISRDNSKNTLYLQMNSL RAEDTAVYYCASEKPGRLGEYDYGSQGTLVTVSSGGGGSGGGS EVQLVESGGGLVQPGNSLRLSCAASGFTFSKFGMSWVRQAPGK GLEWVSSISGSGRDTLYADSVKGRFTISRDNAKTTLYLQMNSLR PEDTAVYYCTIGGSLSVSSQGTLVTVSSGGGGSGGGSEVQLVES GGGLVQPGGSLKLSCAASGFTFNKYAINWVRQAPGKGLEWVAR IRSKYNNYATYYADQVKDRFTISRDDSKNTAYLQMNNLKTEDT AVYYCVRHANFGNSYISYWAYWGQGTLVTVSSGGGGSGGGGS GGGGSQTVVTQEPSLTVSPGGTVTLTCASSTGAVTSGNYPNWV QQKPGQAPRGLIGGTKFLVPGTPARFSGSLLGGKAALTLSGVQP EDEAEYYCTLWYSNRWVFGGGTKLTVLHHHHHH 151 C00404 PSMA PH1 QVQLVESGGGVVQAGRSLRLSCAYSGVTVNVYRMGWFRQAPG TriTAC KEREFVANINWSGNNRDYADSVRGRFTISRDNSKNTLYLQMNSL RAEDTAVYYCASEKPGRLGEYDYGSQGTLVTVSSGGGGSGGGS EVQLVESGGGLVQPGNSLRLSCAASGFTFSKFGMSWVRQAPGK GLEWVSSISGSGRDTLYADSVKGRFTISRDNAKTTLYLQMNSLR PEDTAVYYCTIGGSLSVSSQGTLVTVSSGGGGSGGGSEVQLVES GGGLVQPGGSLKLSCAASGFTFNKYAINWVRQAPGKGLEWVAR IRSKYNNYATYYADQVKDRFTISRDDSKNTAYLQMNNLKTEDT AVYYCVRHANFGNSYISYWAYWGQGTLVTVSSGGGGSGGGGS GGGGSQTVVTQEPSLTVSPGGTVTLTCASSTGAVTSGNYPNWV QQKPGQAPRGLIGGTKFLVPGTPARFSGSLLGGKAALTLSGVQP EDEAEYYCTLWYSNRWVFGGGTKLTVLHHHHHH 152 C00410 PSMA Z2 EVQLVESGGGLVQPGGSLTLSCAASRFMISEYHMHWVRQAPGK TriTAC GLEWVSTINPAGTTDYAESVKGRFTISRDNAKNTLYLQMNSLRA EDTAVYYCDSYGYRGQGTLVTVSSGGGGSGGGSEVQLVESGGG LVQPGNSLRLSCAASGFTFSKFGMSWVRQAPGKGLEWVSSISGS GRDTLYADSVKGRFTISRDNAKTTLYLQMNSLRPEDTAVYYCTI GGSLSVSSQGTLVTVSSGGGGSGGGSEVQLVESGGGLVQPGGSL KLSCAASGFTFNKYAINWVRQAPGKGLEWVARIRSKYNNYATY YADQVKDRFTISRDDSKNTAYLQMNNLKTEDTAVYYCVRHANF GNSYISYWAYWGQGTLVTVSSGGGGSGGGGSGGGGSQTVVTQ EPSLTVSPGGTVTLTCASSTGAVTSGNYPNWVQQKPGQAPRGLI GGTKFLVPGTPARFSGSLLGGKAALTLSGVQPEDEAEYYCTLWY SNRWVFGGGTKLTVLHHHHHH

TABLE-US-00011 TABLE 11 PSMA Binding Domain CDR sequences SEQ ID Nos. Sequence SEQ ID No. 162 RFMISX.sub.1YX.sub.2MH SEQ ID No. 163 X.sub.3INPAX.sub.4X.sub.5TDYAEX.sub.6VKG SEQ ID No. 164 DX.sub.7YGY

TABLE-US-00012 TABLE 12 Exemplary Framework Sequences SEQ ID NO: Description Sequence 165 Framework (f1) EVQLVESGGGLVQPGGSLTLSCAAS 166 Framework (f2) WVRQAPGKGLEWVS 167 Framework (f3) RFTISRDNAKNTLYLQMNSLRAEDTAVYYC 168 Framework (f4) DGYGYRGQGTLVTVSS

[0145] While preferred embodiments of the present invention have been shown and described herein, it will be obvious to those skilled in the art that such embodiments are provided by way of example only. Numerous variations, changes, and substitutions will now occur to those skilled in the art without departing from the invention. It should be understood that various alternatives to the embodiments of the invention described herein may be employed in practicing the invention. It is intended that the following claims define the scope of the invention and that methods and structures within the scope of these claims and their equivalents be covered thereby.

Sequence CWU 1

1

1681249PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 1Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Asn Lys Tyr 20 25 30Ala Ile Asn Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ala Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Ala Thr Tyr Tyr Ala Asp 50 55 60Gln Val Lys Asp Arg Phe Thr Ile Ser Arg Asp Asp Ser Lys Asn Thr65 70 75 80Ala Tyr Leu Gln Met Asn Asn Leu Lys Thr Glu Asp Thr Ala Val Tyr 85 90 95Tyr Cys Val Arg His Ala Asn Phe Gly Asn Ser Tyr Ile Ser Tyr Trp 100 105 110Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly 115 120 125Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gln Thr Val Val 130 135 140Thr Gln Glu Pro Ser Leu Thr Val Ser Pro Gly Gly Thr Val Thr Leu145 150 155 160Thr Cys Ala Ser Ser Thr Gly Ala Val Thr Ser Gly Asn Tyr Pro Asn 165 170 175Trp Val Gln Gln Lys Pro Gly Gln Ala Pro Arg Gly Leu Ile Gly Gly 180 185 190Thr Lys Phe Leu Val Pro Gly Thr Pro Ala Arg Phe Ser Gly Ser Leu 195 200 205Leu Gly Gly Lys Ala Ala Leu Thr Leu Ser Gly Val Gln Pro Glu Asp 210 215 220Glu Ala Glu Tyr Tyr Cys Thr Leu Trp Tyr Ser Asn Arg Trp Val Phe225 230 235 240Gly Gly Gly Thr Lys Leu Thr Val Leu 2452249PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 2Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Glu Phe Asn Lys Tyr 20 25 30Ala Met Asn Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ala Arg Ile Arg Ser Lys Tyr Asn Lys Tyr Ala Thr Tyr Tyr Ala Asp 50 55 60Ser Val Lys Asp Arg Phe Thr Ile Ser Arg Asp Asp Ser Lys Asn Thr65 70 75 80Ala Tyr Leu Gln Met Asn Asn Leu Lys Thr Glu Asp Thr Ala Val Tyr 85 90 95Tyr Cys Val Arg His Gly Asn Phe Gly Asn Ser Tyr Ile Ser Tyr Trp 100 105 110Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly 115 120 125Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gln Thr Val Val 130 135 140Thr Gln Glu Pro Ser Leu Thr Val Ser Pro Gly Gly Thr Val Thr Leu145 150 155 160Thr Cys Gly Ser Ser Phe Gly Ala Val Thr Ser Gly Asn Tyr Pro Asn 165 170 175Trp Val Gln Gln Lys Pro Gly Gln Ala Pro Arg Gly Leu Ile Gly Gly 180 185 190Thr Lys Phe Leu Ala Pro Gly Thr Pro Ala Arg Phe Ser Gly Ser Leu 195 200 205Leu Gly Gly Lys Ala Ala Leu Thr Leu Ser Gly Val Gln Pro Glu Asp 210 215 220Glu Ala Glu Tyr Tyr Cys Val Leu Trp Tyr Asp Asn Arg Trp Val Phe225 230 235 240Gly Gly Gly Thr Lys Leu Thr Val Leu 2453249PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 3Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Asn Lys Tyr 20 25 30Ala Met Asn Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ala Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Ala Thr Tyr Tyr Ala Asp 50 55 60Ser Val Lys Asp Arg Phe Thr Ile Ser Arg Asp Asp Ser Lys Asn Thr65 70 75 80Ala Tyr Leu Gln Met Asn Asn Leu Lys Thr Glu Asp Thr Ala Val Tyr 85 90 95Tyr Cys Val Arg His Gly Asn Phe Gly Asn Ser His Ile Ser Tyr Trp 100 105 110Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly 115 120 125Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gln Thr Val Val 130 135 140Thr Gln Glu Pro Ser Leu Thr Val Ser Pro Gly Gly Thr Val Thr Leu145 150 155 160Thr Cys Gly Ser Ser Thr Gly Tyr Val Thr Ser Gly Asn Tyr Pro Asn 165 170 175Trp Val Gln Gln Lys Pro Gly Gln Ala Pro Arg Gly Leu Ile Gly Gly 180 185 190Thr Ser Phe Leu Ala Pro Gly Thr Pro Ala Arg Phe Ser Gly Ser Leu 195 200 205Leu Gly Gly Lys Ala Ala Leu Thr Leu Ser Gly Val Gln Pro Glu Asp 210 215 220Glu Ala Glu Tyr Tyr Cys Val Leu Trp Tyr Ser Asn Arg Trp Ile Phe225 230 235 240Gly Gly Gly Thr Lys Leu Thr Val Leu 2454249PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 4Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Met Phe Asn Lys Tyr 20 25 30Ala Met Asn Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ala Arg Ile Arg Ser Lys Ser Asn Asn Tyr Ala Thr Tyr Tyr Ala Asp 50 55 60Ser Val Lys Asp Arg Phe Thr Ile Ser Arg Asp Asp Ser Lys Asn Thr65 70 75 80Ala Tyr Leu Gln Met Asn Asn Leu Lys Thr Glu Asp Thr Ala Val Tyr 85 90 95Tyr Cys Val Arg His Gly Asn Phe Gly Asn Ser Tyr Ile Ser Tyr Trp 100 105 110Ala Thr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly 115 120 125Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gln Thr Val Val 130 135 140Thr Gln Glu Pro Ser Leu Thr Val Ser Pro Gly Gly Thr Val Thr Leu145 150 155 160Thr Cys Gly Ser Ser Phe Gly Ala Val Thr Ser Gly Asn Tyr Pro Asn 165 170 175Trp Val Gln Gln Lys Pro Gly Gln Ala Pro Arg Gly Leu Ile Gly Gly 180 185 190Thr Lys Leu Leu Ala Pro Gly Thr Pro Ala Arg Phe Ser Gly Ser Leu 195 200 205Leu Gly Gly Lys Ala Ala Leu Thr Leu Ser Gly Val Gln Pro Glu Asp 210 215 220Glu Ala Glu Tyr Tyr Cys Val Leu Trp Tyr Ser Asn Ser Trp Val Phe225 230 235 240Gly Gly Gly Thr Lys Leu Thr Val Leu 2455249PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 5Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Asn Thr Tyr 20 25 30Ala Met Asn Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ala Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Ala Thr Tyr Tyr Lys Asp 50 55 60Ser Val Lys Asp Arg Phe Thr Ile Ser Arg Asp Asp Ser Lys Asn Thr65 70 75 80Ala Tyr Leu Gln Met Asn Asn Leu Lys Thr Glu Asp Thr Ala Val Tyr 85 90 95Tyr Cys Val Arg His Gly Asn Phe Gly Asn Ser Pro Ile Ser Tyr Trp 100 105 110Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly 115 120 125Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gln Thr Val Val 130 135 140Thr Gln Glu Pro Ser Leu Thr Val Ser Pro Gly Gly Thr Val Thr Leu145 150 155 160Thr Cys Gly Ser Ser Thr Gly Ala Val Val Ser Gly Asn Tyr Pro Asn 165 170 175Trp Val Gln Gln Lys Pro Gly Gln Ala Pro Arg Gly Leu Ile Gly Gly 180 185 190Thr Glu Phe Leu Ala Pro Gly Thr Pro Ala Arg Phe Ser Gly Ser Leu 195 200 205Leu Gly Gly Lys Ala Ala Leu Thr Leu Ser Gly Val Gln Pro Glu Asp 210 215 220Glu Ala Glu Tyr Tyr Cys Val Leu Trp Tyr Ser Asn Arg Trp Val Phe225 230 235 240Gly Gly Gly Thr Lys Leu Thr Val Leu 2456249PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 6Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Thr Tyr Asn Lys Tyr 20 25 30Ala Met Asn Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ala Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Ala Thr Tyr Tyr Ala Asp 50 55 60Glu Val Lys Asp Arg Phe Thr Ile Ser Arg Asp Asp Ser Lys Asn Thr65 70 75 80Ala Tyr Leu Gln Met Asn Asn Leu Lys Thr Glu Asp Thr Ala Val Tyr 85 90 95Tyr Cys Val Arg His Gly Asn Phe Gly Asn Ser Pro Ile Ser Tyr Trp 100 105 110Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly 115 120 125Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gln Thr Val Val 130 135 140Thr Gln Glu Pro Ser Leu Thr Val Ser Pro Gly Gly Thr Val Thr Leu145 150 155 160Thr Cys Gly Ser Ser Lys Gly Ala Val Thr Ser Gly Asn Tyr Pro Asn 165 170 175Trp Val Gln Gln Lys Pro Gly Gln Ala Pro Arg Gly Leu Ile Gly Gly 180 185 190Thr Lys Glu Leu Ala Pro Gly Thr Pro Ala Arg Phe Ser Gly Ser Leu 195 200 205Leu Gly Gly Lys Ala Ala Leu Thr Leu Ser Gly Val Gln Pro Glu Asp 210 215 220Glu Ala Glu Tyr Tyr Cys Thr Leu Trp Tyr Ser Asn Arg Trp Val Phe225 230 235 240Gly Gly Gly Thr Lys Leu Thr Val Leu 2457249PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 7Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Asn Thr Phe Asn Lys Tyr 20 25 30Ala Met Asn Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ala Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Glu Thr Tyr Tyr Ala Asp 50 55 60Ser Val Lys Asp Arg Phe Thr Ile Ser Arg Asp Asp Ser Lys Asn Thr65 70 75 80Ala Tyr Leu Gln Met Asn Asn Leu Lys Thr Glu Asp Thr Ala Val Tyr 85 90 95Tyr Cys Val Arg His Thr Asn Phe Gly Asn Ser Tyr Ile Ser Tyr Trp 100 105 110Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly 115 120 125Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gln Thr Val Val 130 135 140Thr Gln Glu Pro Ser Leu Thr Val Ser Pro Gly Gly Thr Val Thr Leu145 150 155 160Thr Cys Gly Ser Ser Thr Gly Ala Val Thr Ser Gly Tyr Tyr Pro Asn 165 170 175Trp Val Gln Gln Lys Pro Gly Gln Ala Pro Arg Gly Leu Ile Gly Gly 180 185 190Thr Tyr Phe Leu Ala Pro Gly Thr Pro Ala Arg Phe Ser Gly Ser Leu 195 200 205Leu Gly Gly Lys Ala Ala Leu Thr Leu Ser Gly Val Gln Pro Glu Asp 210 215 220Glu Ala Glu Tyr Tyr Cys Val Leu Trp Tyr Ser Asn Arg Trp Val Phe225 230 235 240Gly Gly Gly Thr Lys Leu Thr Val Leu 2458249PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 8Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Asn Asn Tyr 20 25 30Ala Met Asn Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ala Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Ala Thr Tyr Tyr Ala Asp 50 55 60Ala Val Lys Asp Arg Phe Thr Ile Ser Arg Asp Asp Ser Lys Asn Thr65 70 75 80Ala Tyr Leu Gln Met Asn Asn Leu Lys Thr Glu Asp Thr Ala Val Tyr 85 90 95Tyr Cys Val Arg His Gly Asn Phe Gly Asn Ser Gln Ile Ser Tyr Trp 100 105 110Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly 115 120 125Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gln Thr Val Val 130 135 140Thr Gln Glu Pro Ser Leu Thr Val Ser Pro Gly Gly Thr Val Thr Leu145 150 155 160Thr Cys Gly Ser Ser Thr Gly Ala Val Thr Asp Gly Asn Tyr Pro Asn 165 170 175Trp Val Gln Gln Lys Pro Gly Gln Ala Pro Arg Gly Leu Ile Gly Gly 180 185 190Ile Lys Phe Leu Ala Pro Gly Thr Pro Ala Arg Phe Ser Gly Ser Leu 195 200 205Leu Gly Gly Lys Ala Ala Leu Thr Leu Ser Gly Val Gln Pro Glu Asp 210 215 220Glu Ala Glu Tyr Tyr Cys Val Leu Trp Tyr Ser Asn Arg Trp Val Phe225 230 235 240Gly Gly Gly Thr Lys Leu Thr Val Leu 2459249PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 9Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Asn Lys Tyr 20 25 30Ala Val Asn Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ala Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Ala Thr Tyr Tyr Ala Asp 50 55 60Ser Val Lys Asp Arg Phe Thr Ile Ser Arg Asp Asp Ser Lys Asn Thr65 70 75 80Ala Tyr Leu Gln Met Asn Asn Leu Lys Thr Glu Asp Thr Ala Val Tyr 85 90 95Tyr Cys Val Arg His Gly Asn Phe Gly Asn Ser Tyr Ile Ser Tyr Trp 100 105 110Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly 115 120 125Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gln Thr Val Val 130 135 140Thr Gln Glu Pro Ser Leu Thr Val Ser Pro Gly Gly Thr Val Thr Leu145 150 155 160Thr Cys Gly Glu Ser Thr Gly Ala Val Thr Ser Gly Asn Tyr Pro Asn 165 170 175Trp Val Gln Gln Lys Pro Gly Gln Ala Pro Arg Gly Leu Ile Gly Gly 180 185 190Thr Lys Ile Leu Ala Pro Gly Thr Pro Ala Arg Phe Ser Gly Ser Leu 195 200 205Leu Gly Gly Lys Ala Ala Leu Thr Leu Ser Gly Val Gln Pro Glu Asp 210 215 220Glu Ala Glu Tyr Tyr Cys Val Leu Trp Tyr Ser Asn Arg Trp Val Phe225 230 235 240Gly Gly Gly Thr Lys Leu Thr Val Leu 24510249PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 10Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Asn Lys Tyr 20 25 30Pro Met Asn Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ala Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Ala Thr Tyr Tyr Ala Asp 50 55 60Ser Val Lys Asp Arg Phe Thr Ile Ser Arg Asp Asp Ser Lys Asn Thr65 70 75 80Ala Tyr Leu Gln Met Asn Asn Leu Lys Asn Glu Asp Thr Ala Val Tyr 85 90 95Tyr Cys Val Arg His Gly Asn Phe Asn Asn Ser Tyr Ile Ser Tyr Trp 100 105 110Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly 115 120

125Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gln Thr Val Val 130 135 140Thr Gln Glu Pro Ser Leu Thr Val Ser Pro Gly Gly Thr Val Thr Leu145 150 155 160Thr Cys Gly Ser Ser Thr Gly Ala Val Thr Lys Gly Asn Tyr Pro Asn 165 170 175Trp Val Gln Gln Lys Pro Gly Gln Ala Pro Arg Gly Leu Ile Gly Gly 180 185 190Thr Lys Met Leu Ala Pro Gly Thr Pro Ala Arg Phe Ser Gly Ser Leu 195 200 205Leu Gly Gly Lys Ala Ala Leu Thr Leu Ser Gly Val Gln Pro Glu Asp 210 215 220Glu Ala Glu Tyr Tyr Cys Ala Leu Trp Tyr Ser Asn Arg Trp Val Phe225 230 235 240Gly Gly Gly Thr Lys Leu Thr Val Leu 24511249PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 11Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Asn Gly Tyr 20 25 30Ala Met Asn Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ala Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Ala Thr Tyr Tyr Ala Asp 50 55 60Glu Val Lys Asp Arg Phe Thr Ile Ser Arg Asp Asp Ser Lys Asn Thr65 70 75 80Ala Tyr Leu Gln Met Asn Asn Leu Lys Thr Glu Asp Thr Ala Val Tyr 85 90 95Tyr Cys Val Arg His Gly Asn Phe Gly Asn Ser Pro Ile Ser Tyr Trp 100 105 110Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly 115 120 125Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gln Thr Val Val 130 135 140Thr Gln Glu Pro Ser Leu Thr Val Ser Pro Gly Gly Thr Val Thr Leu145 150 155 160Thr Cys Gly Ser Ser Thr Gly Ala Val Val Ser Gly Asn Tyr Pro Asn 165 170 175Trp Val Gln Gln Lys Pro Gly Gln Ala Pro Arg Gly Leu Ile Gly Gly 180 185 190Thr Glu Phe Leu Ala Pro Gly Thr Pro Ala Arg Phe Ser Gly Ser Leu 195 200 205Leu Gly Gly Lys Ala Ala Leu Thr Leu Ser Gly Val Gln Pro Glu Asp 210 215 220Glu Ala Glu Tyr Tyr Cys Val Leu Trp Tyr Ser Asn Arg Trp Val Phe225 230 235 240Gly Gly Gly Thr Lys Leu Thr Val Leu 24512249PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 12Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Asn Thr Phe Asn Lys Tyr 20 25 30Ala Met Asn Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ala Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Ala Thr Tyr Tyr Ala Asp 50 55 60Ser Val Lys Asp Arg Phe Thr Ile Ser Arg Asp Asp Ser Lys Asn Thr65 70 75 80Ala Tyr Leu Gln Met Asn Asn Leu Lys Thr Glu Asp Thr Ala Val Tyr 85 90 95Tyr Cys Val Arg His Gly Asn Phe Gly Asp Ser Tyr Ile Ser Tyr Trp 100 105 110Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly 115 120 125Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gln Thr Val Val 130 135 140Thr Gln Glu Pro Ser Leu Thr Val Ser Pro Gly Gly Thr Val Thr Leu145 150 155 160Thr Cys Gly Ser Ser Thr Gly Ala Val Thr His Gly Asn Tyr Pro Asn 165 170 175Trp Val Gln Gln Lys Pro Gly Gln Ala Pro Arg Gly Leu Ile Gly Gly 180 185 190Thr Lys Val Leu Ala Pro Gly Thr Pro Ala Arg Phe Ser Gly Ser Leu 195 200 205Leu Gly Gly Lys Ala Ala Leu Thr Leu Ser Gly Val Gln Pro Glu Asp 210 215 220Glu Ala Glu Tyr Tyr Cys Val Leu Trp Tyr Ser Asn Arg Trp Val Phe225 230 235 240Gly Gly Gly Thr Lys Leu Thr Val Leu 24513249PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 13Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Asn Asn Tyr 20 25 30Ala Met Asn Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ala Arg Ile Arg Ser Gly Tyr Asn Asn Tyr Ala Thr Tyr Tyr Ala Asp 50 55 60Ser Val Lys Asp Arg Phe Thr Ile Ser Arg Asp Asp Ser Lys Asn Thr65 70 75 80Ala Tyr Leu Gln Met Asn Asn Leu Lys Thr Glu Asp Thr Ala Val Tyr 85 90 95Tyr Cys Val Arg His Gly Asn Phe Gly Asn Ser Tyr Ile Ser Tyr Trp 100 105 110Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly 115 120 125Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gln Thr Val Val 130 135 140Thr Gln Glu Pro Ser Leu Thr Val Ser Pro Gly Gly Thr Val Thr Leu145 150 155 160Thr Cys Gly Ser Tyr Thr Gly Ala Val Thr Ser Gly Asn Tyr Pro Asn 165 170 175Trp Val Gln Gln Lys Pro Gly Gln Ala Pro Arg Gly Leu Ile Gly Gly 180 185 190Thr Lys Phe Asn Ala Pro Gly Thr Pro Ala Arg Phe Ser Gly Ser Leu 195 200 205Leu Gly Gly Lys Ala Ala Leu Thr Leu Ser Gly Val Gln Pro Glu Asp 210 215 220Glu Ala Glu Tyr Tyr Cys Val Leu Trp Tyr Ala Asn Arg Trp Val Phe225 230 235 240Gly Gly Gly Thr Lys Leu Thr Val Leu 24514249PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 14Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Glu Phe Asn Lys Tyr 20 25 30Ala Met Asn Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ala Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Glu Thr Tyr Tyr Ala Asp 50 55 60Ser Val Lys Asp Arg Phe Thr Ile Ser Arg Asp Asp Ser Lys Asn Thr65 70 75 80Ala Tyr Leu Gln Met Asn Asn Leu Lys Thr Glu Asp Thr Ala Val Tyr 85 90 95Tyr Cys Val Arg His Gly Asn Phe Gly Asn Ser Leu Ile Ser Tyr Trp 100 105 110Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly 115 120 125Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gln Thr Val Val 130 135 140Thr Gln Glu Pro Ser Leu Thr Val Ser Pro Gly Gly Thr Val Thr Leu145 150 155 160Thr Cys Gly Ser Ser Ser Gly Ala Val Thr Ser Gly Asn Tyr Pro Asn 165 170 175Trp Val Gln Gln Lys Pro Gly Gln Ala Pro Arg Gly Leu Ile Gly Gly 180 185 190Thr Lys Phe Gly Ala Pro Gly Thr Pro Ala Arg Phe Ser Gly Ser Leu 195 200 205Leu Gly Gly Lys Ala Ala Leu Thr Leu Ser Gly Val Gln Pro Glu Asp 210 215 220Glu Ala Glu Tyr Tyr Cys Val Leu Trp Tyr Ser Asn Arg Trp Val Phe225 230 235 240Gly Gly Gly Thr Lys Leu Thr Val Leu 24515249PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 15Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Asn Lys Tyr 20 25 30Ala Met Asn Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ala Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Ala Thr Tyr Tyr Ala Asp 50 55 60Ser Val Lys Asp Arg Phe Thr Ile Ser Arg Asp Asp Ser Lys Asn Thr65 70 75 80Ala Tyr Leu Gln Met Asn Asn Leu Lys Thr Glu Asp Thr Ala Val Tyr 85 90 95Tyr Cys Val Arg His Gly Asn Phe Gly Asn Ser Tyr Ile Ser Tyr Trp 100 105 110Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly 115 120 125Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gln Thr Val Val 130 135 140Thr Gln Glu Pro Ser Leu Thr Val Ser Pro Gly Gly Thr Val Thr Leu145 150 155 160Thr Cys Gly Ser Ser Thr Gly Ala Val Thr Ser Gly Asn Tyr Pro Asn 165 170 175Trp Val Gln Gln Lys Pro Gly Gln Ala Pro Arg Gly Leu Ile Gly Gly 180 185 190Thr Lys Phe Leu Ala Pro Gly Thr Pro Ala Arg Phe Ser Gly Ser Leu 195 200 205Leu Gly Gly Lys Ala Ala Leu Thr Leu Ser Gly Val Gln Pro Glu Asp 210 215 220Glu Ala Glu Tyr Tyr Cys Val Leu Trp Tyr Ser Asn Arg Trp Val Phe225 230 235 240Gly Gly Gly Thr Lys Leu Thr Val Leu 2451610PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 16Gly Phe Thr Phe Asn Lys Tyr Ala Met Asn1 5 101718PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 17Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Ala Thr Tyr Tyr Ala Asp Ser1 5 10 15Val Lys1814PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 18His Gly Asn Phe Gly Asn Ser Tyr Ile Ser Tyr Trp Ala Tyr1 5 101914PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 19Gly Ser Ser Thr Gly Ala Val Thr Ser Gly Asn Tyr Pro Asn1 5 10207PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 20Gly Thr Lys Phe Leu Ala Pro1 5219PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 21Val Leu Trp Tyr Ser Asn Arg Trp Val1 52210PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 22Gly Asn Thr Phe Asn Lys Tyr Ala Met Asn1 5 102310PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 23Gly Phe Glu Phe Asn Lys Tyr Ala Met Asn1 5 102410PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 24Gly Phe Met Phe Asn Lys Tyr Ala Met Asn1 5 102510PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 25Gly Phe Thr Tyr Asn Lys Tyr Ala Met Asn1 5 102610PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 26Gly Phe Thr Phe Asn Asn Tyr Ala Met Asn1 5 102710PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 27Gly Phe Thr Phe Asn Gly Tyr Ala Met Asn1 5 102810PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 28Gly Phe Thr Phe Asn Thr Tyr Ala Met Asn1 5 102910PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 29Gly Phe Thr Phe Asn Glu Tyr Ala Met Asn1 5 103010PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 30Gly Phe Thr Phe Asn Lys Tyr Pro Met Asn1 5 103110PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 31Gly Phe Thr Phe Asn Lys Tyr Ala Val Asn1 5 103210PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 32Gly Phe Thr Phe Asn Lys Tyr Ala Ile Asn1 5 103310PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 33Gly Phe Thr Phe Asn Lys Tyr Ala Leu Asn1 5 103418PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 34Arg Ile Arg Ser Gly Tyr Asn Asn Tyr Ala Thr Tyr Tyr Ala Asp Ser1 5 10 15Val Lys3518PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 35Arg Ile Arg Ser Lys Ser Asn Asn Tyr Ala Thr Tyr Tyr Ala Asp Ser1 5 10 15Val Lys3618PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 36Arg Ile Arg Ser Lys Tyr Asn Lys Tyr Ala Thr Tyr Tyr Ala Asp Ser1 5 10 15Val Lys3718PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 37Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Glu Thr Tyr Tyr Ala Asp Ser1 5 10 15Val Lys3818PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 38Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Ala Thr Glu Tyr Ala Asp Ser1 5 10 15Val Lys3918PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 39Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Ala Thr Tyr Tyr Lys Asp Ser1 5 10 15Val Lys4018PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 40Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Ala Thr Tyr Tyr Ala Asp Glu1 5 10 15Val Lys4118PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 41Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Ala Thr Tyr Tyr Ala Asp Ala1 5 10 15Val Lys4218PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 42Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Ala Thr Tyr Tyr Ala Asp Gln1 5 10 15Val Lys4318PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 43Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Ala Thr Tyr Tyr Ala Asp Asp1 5 10 15Val Lys4414PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 44His Ala Asn Phe Gly Asn Ser Tyr Ile Ser Tyr Trp Ala Tyr1 5 104514PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 45His Thr Asn Phe Gly Asn Ser Tyr Ile Ser Tyr Trp Ala Tyr1 5 104614PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 46His Gly Asn Phe Asn Asn Ser Tyr Ile Ser Tyr Trp Ala Tyr1 5 104714PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 47His Gly Asn Phe Gly Asp Ser Tyr Ile Ser Tyr Trp Ala Tyr1 5 104814PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 48His Gly Asn Phe Gly Asn Ser His Ile Ser Tyr Trp Ala Tyr1 5 104914PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 49His Gly Asn Phe Gly Asn Ser Pro Ile Ser Tyr Trp Ala Tyr1 5 105014PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 50His Gly Asn Phe Gly Asn Ser Gln Ile Ser Tyr Trp Ala Tyr1 5 105114PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 51His Gly Asn Phe Gly Asn Ser Leu Ile Ser Tyr Trp Ala Tyr1 5 105214PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 52His Gly Asn Phe Gly Asn Ser Gly Ile Ser Tyr Trp Ala Tyr1 5 105314PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 53His Gly Asn Phe Gly Asn Ser Tyr Ile Ser Tyr Trp Ala Thr1 5 105414PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 54Ala Ser Ser Thr Gly Ala Val Thr Ser Gly Asn Tyr Pro Asn1 5 105514PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 55Gly Glu Ser Thr Gly Ala Val Thr Ser Gly Asn Tyr Pro Asn1 5 105614PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 56Gly Ser Tyr Thr Gly Ala Val Thr Ser Gly Asn Tyr Pro Asn1 5 105714PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 57Gly Ser Ser Phe Gly Ala Val

Thr Ser Gly Asn Tyr Pro Asn1 5 105814PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 58Gly Ser Ser Lys Gly Ala Val Thr Ser Gly Asn Tyr Pro Asn1 5 105914PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 59Gly Ser Ser Ser Gly Ala Val Thr Ser Gly Asn Tyr Pro Asn1 5 106014PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 60Gly Ser Ser Thr Gly Tyr Val Thr Ser Gly Asn Tyr Pro Asn1 5 106114PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 61Gly Ser Ser Thr Gly Ala Val Val Ser Gly Asn Tyr Pro Asn1 5 106214PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 62Gly Ser Ser Thr Gly Ala Val Thr Asp Gly Asn Tyr Pro Asn1 5 106314PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 63Gly Ser Ser Thr Gly Ala Val Thr Lys Gly Asn Tyr Pro Asn1 5 106414PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 64Gly Ser Ser Thr Gly Ala Val Thr His Gly Asn Tyr Pro Asn1 5 106514PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 65Gly Ser Ser Thr Gly Ala Val Thr Val Gly Asn Tyr Pro Asn1 5 106614PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 66Gly Ser Ser Thr Gly Ala Val Thr Ser Gly Tyr Tyr Pro Asn1 5 10677PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 67Gly Ile Lys Phe Leu Ala Pro1 5687PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 68Gly Thr Glu Phe Leu Ala Pro1 5697PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 69Gly Thr Tyr Phe Leu Ala Pro1 5707PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 70Gly Thr Ser Phe Leu Ala Pro1 5717PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 71Gly Thr Asn Phe Leu Ala Pro1 5727PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 72Gly Thr Lys Leu Leu Ala Pro1 5737PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 73Gly Thr Lys Glu Leu Ala Pro1 5747PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 74Gly Thr Lys Ile Leu Ala Pro1 5757PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 75Gly Thr Lys Met Leu Ala Pro1 5767PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 76Gly Thr Lys Val Leu Ala Pro1 5777PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 77Gly Thr Lys Phe Asn Ala Pro1 5787PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 78Gly Thr Lys Phe Gly Ala Pro1 5797PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 79Gly Thr Lys Phe Leu Val Pro1 5809PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 80Thr Leu Trp Tyr Ser Asn Arg Trp Val1 5819PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 81Ala Leu Trp Tyr Ser Asn Arg Trp Val1 5829PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 82Val Leu Trp Tyr Asp Asn Arg Trp Val1 5839PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 83Val Leu Trp Tyr Ala Asn Arg Trp Val1 5849PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 84Val Leu Trp Tyr Ser Asn Ser Trp Val1 5859PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 85Val Leu Trp Tyr Ser Asn Arg Trp Ile1 5869PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 86Val Leu Trp Tyr Ser Asn Arg Trp Ala1 587249PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 87Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Asn Lys Tyr 20 25 30Ala Leu Asn Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ala Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Ala Thr Glu Tyr Ala Asp 50 55 60Ser Val Lys Asp Arg Phe Thr Ile Ser Arg Asp Asp Ser Lys Asn Thr65 70 75 80Ala Tyr Leu Gln Met Asn Asn Leu Lys Thr Glu Asp Thr Ala Val Tyr 85 90 95Tyr Cys Val Arg His Gly Asn Phe Gly Asn Ser Pro Ile Ser Tyr Trp 100 105 110Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly 115 120 125Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gln Thr Val Val 130 135 140Thr Gln Glu Pro Ser Leu Thr Val Ser Pro Gly Gly Thr Val Thr Leu145 150 155 160Thr Cys Gly Ser Ser Thr Gly Ala Val Thr Ser Gly Asn Tyr Pro Asn 165 170 175Trp Val Gln Gln Lys Pro Gly Gln Ala Pro Arg Gly Leu Ile Gly Gly 180 185 190Thr Asn Phe Leu Ala Pro Gly Thr Pro Glu Arg Phe Ser Gly Ser Leu 195 200 205Leu Gly Gly Lys Ala Ala Leu Thr Leu Ser Gly Val Gln Pro Glu Asp 210 215 220Glu Ala Glu Tyr Tyr Cys Val Leu Trp Tyr Ser Asn Arg Trp Ala Phe225 230 235 240Gly Gly Gly Thr Lys Leu Thr Val Leu 24588249PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 88Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Asn Glu Tyr 20 25 30Ala Met Asn Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ala Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Ala Thr Tyr Tyr Ala Asp 50 55 60Asp Val Lys Asp Arg Phe Thr Ile Ser Arg Asp Asp Ser Lys Asn Thr65 70 75 80Ala Tyr Leu Gln Met Asn Asn Leu Lys Thr Glu Asp Thr Ala Val Tyr 85 90 95Tyr Cys Val Arg His Gly Asn Phe Gly Asn Ser Gly Ile Ser Tyr Trp 100 105 110Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly 115 120 125Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gln Thr Val Val 130 135 140Thr Gln Glu Pro Ser Leu Thr Val Ser Pro Gly Gly Thr Val Thr Leu145 150 155 160Thr Cys Gly Ser Ser Thr Gly Ala Val Thr Val Gly Asn Tyr Pro Asn 165 170 175Trp Val Gln Gln Lys Pro Gly Gln Ala Pro Arg Gly Leu Ile Gly Gly 180 185 190Thr Glu Phe Leu Ala Pro Gly Thr Pro Ala Arg Phe Ser Gly Ser Leu 195 200 205Leu Gly Gly Lys Ala Ala Leu Thr Leu Ser Gly Val Gln Pro Glu Asp 210 215 220Glu Ala Glu Tyr Tyr Cys Val Leu Trp Tyr Ser Asn Arg Trp Val Phe225 230 235 240Gly Gly Gly Thr Lys Leu Thr Val Leu 24589115PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 89Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Asn1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Arg Phe 20 25 30Gly Met Ser Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Ser Ile Ser Gly Ser Gly Ser Asp Thr Leu Tyr Ala Asp Ser Val 50 55 60Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Thr Thr Leu Tyr65 70 75 80Leu Gln Met Asn Ser Leu Arg Pro Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Thr Ile Gly Gly Ser Leu Ser Arg Ser Ser Gln Gly Thr Leu Val Thr 100 105 110Val Ser Ser 11590115PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 90Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Asn1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Lys Phe 20 25 30Gly Met Ser Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Ser Ile Ser Gly Ser Gly Ala Asp Thr Leu Tyr Ala Asp Ser Leu 50 55 60Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Thr Thr Leu Tyr65 70 75 80Leu Gln Met Asn Ser Leu Arg Pro Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Thr Ile Gly Gly Ser Leu Ser Lys Ser Ser Gln Gly Thr Leu Val Thr 100 105 110Val Ser Ser 11591115PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 91Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Asn1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Tyr Ser Ser Phe 20 25 30Gly Met Ser Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Ser Ile Ser Gly Ser Gly Ser Asp Thr Leu Tyr Ala Asp Ser Val 50 55 60Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Thr Thr Leu Tyr65 70 75 80Leu Gln Met Asn Ser Leu Arg Pro Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Thr Ile Gly Gly Ser Leu Ser Lys Ser Ser Gln Gly Thr Leu Val Thr 100 105 110Val Ser Ser 11592115PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 92Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Asn1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Lys Phe 20 25 30Gly Met Ser Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Ser Ile Ser Gly Ser Gly Thr Asp Thr Leu Tyr Ala Asp Ser Val 50 55 60Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Thr Thr Leu Tyr65 70 75 80Leu Gln Met Asn Ser Leu Arg Pro Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Thr Ile Gly Gly Ser Leu Ser Arg Ser Ser Gln Gly Thr Leu Val Thr 100 105 110Val Ser Ser 11593115PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 93Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Asn1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Arg Phe 20 25 30Gly Met Ser Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Ser Ile Ser Gly Ser Gly Ser Asp Thr Leu Tyr Ala Asp Ser Val 50 55 60Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Thr Thr Leu Tyr65 70 75 80Leu Gln Met Asn Ser Leu Arg Pro Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Thr Ile Gly Gly Ser Leu Ser Lys Ser Ser Gln Gly Thr Leu Val Thr 100 105 110Val Ser Ser 11594115PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 94Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Asn1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Lys Phe 20 25 30Gly Met Ser Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Ser Ile Ser Gly Ser Gly Arg Asp Thr Leu Tyr Ala Asp Ser Val 50 55 60Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Thr Thr Leu Tyr65 70 75 80Leu Gln Met Asn Ser Leu Arg Pro Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Thr Ile Gly Gly Ser Leu Ser Val Ser Ser Gln Gly Thr Leu Val Thr 100 105 110Val Ser Ser 11595115PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 95Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Asn1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Ser Phe 20 25 30Gly Met Ser Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Ser Ile Ser Gly Ser Gly Ser Asp Thr Leu Tyr Ala Asp Ser Val 50 55 60Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Thr Thr Leu Tyr65 70 75 80Leu Gln Met Asn Ser Leu Arg Pro Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Thr Ile Gly Gly Ser Leu Ser Arg Ser Ser Gln Gly Thr Leu Val Thr 100 105 110Val Ser Ser 1159610PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 96Gly Phe Thr Phe Ser Ser Phe Gly Met Ser1 5 109716PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 97Ser Ile Ser Gly Ser Gly Ser Asp Thr Leu Tyr Ala Asp Ser Val Lys1 5 10 15986PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 98Gly Gly Ser Leu Ser Arg1 59910PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 99Gly Phe Thr Phe Ser Arg Phe Gly Met Ser1 5 1010010PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 100Gly Phe Thr Phe Ser Lys Phe Gly Met Ser1 5 1010110PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 101Gly Phe Thr Tyr Ser Ser Phe Gly Met Ser1 5 1010216PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 102Ser Ile Ser Gly Ser Gly Ala Asp Thr Leu Tyr Ala Asp Ser Leu Lys1 5 10 1510316PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 103Ser Ile Ser Gly Ser Gly Thr Asp Thr Leu Tyr Ala Asp Ser Val Lys1 5 10 1510416PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 104Ser Ile Ser Gly Ser Gly Arg Asp Thr Leu Tyr Ala Asp Ser Val Lys1 5 10 1510516PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 105Ser Ile Ser Gly Ser Gly Ser Asp Thr Leu Tyr Ala Glu Ser Val Lys1 5 10 1510616PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 106Ser Ile Ser Gly Ser Gly Thr Asp Thr Leu Tyr Ala Glu Ser Val Lys1 5 10 1510716PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 107Ser Ile Ser Gly Ser Gly Arg Asp Thr Leu Tyr Ala Glu Ser Val Lys1 5 10 151086PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 108Gly Gly Ser Leu Ser Lys1 51096PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 109Gly Gly Ser Leu Ser Val1 5110115PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 110Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Asn1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Arg Phe 20 25 30Gly Met Ser Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Ser Ile Ser Gly Ser Gly Ser Asp Thr Leu Tyr Ala Glu Ser Val 50 55 60Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Thr Thr Leu Tyr65 70 75

80Leu Gln Met Asn Ser Leu Arg Pro Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Thr Ile Gly Gly Ser Leu Ser Arg Ser Ser Gln Gly Thr Leu Val Thr 100 105 110Val Ser Ser 115111115PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 111Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Asn1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Lys Phe 20 25 30Gly Met Ser Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Ser Ile Ser Gly Ser Gly Thr Asp Thr Leu Tyr Ala Glu Ser Val 50 55 60Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Thr Thr Leu Tyr65 70 75 80Leu Gln Met Asn Ser Leu Arg Pro Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Thr Ile Gly Gly Ser Leu Ser Arg Ser Ser Gln Gly Thr Leu Val Thr 100 105 110Val Ser Ser 115112115PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 112Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Asn1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Lys Phe 20 25 30Gly Met Ser Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Ser Ile Ser Gly Ser Gly Arg Asp Thr Leu Tyr Ala Glu Ser Val 50 55 60Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Thr Thr Leu Tyr65 70 75 80Leu Gln Met Asn Ser Leu Arg Pro Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Thr Ile Gly Gly Ser Leu Ser Val Ser Ser Gln Gly Thr Leu Val Thr 100 105 110Val Ser Ser 115113111PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 113Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Thr Leu Ser Cys Ala Ala Ser Arg Phe Met Ile Ser Glu Tyr 20 25 30Ser Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Thr Ile Asn Pro Ala Gly Thr Thr Asp Tyr Ala Glu Ser Val Lys 50 55 60Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr Leu65 70 75 80Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Tyr Cys Asp 85 90 95Gly Tyr Gly Tyr Arg Gly Gln Gly Thr Gln Val Thr Val Ser Ser 100 105 11011410PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 114Arg Phe Met Ile Ser Glu Tyr His Met His1 5 1011510PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 115Arg Phe Met Ile Ser Pro Tyr Ser Met His1 5 1011610PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 116Arg Phe Met Ile Ser Pro Tyr His Met His1 5 1011716PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 117Asp Ile Asn Pro Ala Gly Thr Thr Asp Tyr Ala Glu Ser Val Lys Gly1 5 10 1511816PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 118Thr Ile Asn Pro Ala Lys Thr Thr Asp Tyr Ala Glu Ser Val Lys Gly1 5 10 1511916PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 119Thr Ile Asn Pro Ala Gly Gln Thr Asp Tyr Ala Glu Ser Val Lys Gly1 5 10 1512016PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 120Thr Ile Asn Pro Ala Gly Thr Thr Asp Tyr Ala Glu Tyr Val Lys Gly1 5 10 1512116PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 121Asp Ile Asn Pro Ala Lys Thr Thr Asp Tyr Ala Glu Ser Val Lys Gly1 5 10 1512216PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 122Asp Ile Asn Pro Ala Gly Gln Thr Asp Tyr Ala Glu Ser Val Lys Gly1 5 10 1512316PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 123Asp Ile Asn Pro Ala Gly Thr Thr Asp Tyr Ala Glu Tyr Val Lys Gly1 5 10 151245PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 124Asp Ser Tyr Gly Tyr1 512510PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 125Arg Phe Met Ile Ser Glu Tyr Ser Met His1 5 1012616PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 126Thr Ile Asn Pro Ala Gly Thr Thr Asp Tyr Ala Glu Ser Val Lys Gly1 5 10 151275PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 127Asp Gly Tyr Gly Tyr1 5128111PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 128Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser Arg Phe Met Ile Ser Glu Tyr 20 25 30Ser Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Thr Ile Asn Pro Ala Gly Thr Thr Asp Tyr Ala Glu Ser Val Lys 50 55 60Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr Leu65 70 75 80Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys Asp 85 90 95Gly Tyr Gly Tyr Arg Gly Gln Gly Thr Leu Val Thr Val Ser Ser 100 105 110129111PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 129Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser Arg Phe Met Ile Ser Glu Tyr 20 25 30His Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Asp Ile Asn Pro Ala Gly Thr Thr Asp Tyr Ala Glu Ser Val Lys 50 55 60Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr Leu65 70 75 80Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys Asp 85 90 95Ser Tyr Gly Tyr Arg Gly Gln Gly Thr Leu Val Thr Val Ser Ser 100 105 110130111PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 130Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser Arg Phe Met Ile Ser Glu Tyr 20 25 30His Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Thr Ile Asn Pro Ala Gly Thr Thr Asp Tyr Ala Glu Ser Val Lys 50 55 60Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr Leu65 70 75 80Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys Asp 85 90 95Ser Tyr Gly Tyr Arg Gly Gln Gly Thr Leu Val Thr Val Ser Ser 100 105 110131111PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 131Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser Arg Phe Met Ile Ser Glu Tyr 20 25 30Ser Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Thr Ile Asn Pro Ala Lys Thr Thr Asp Tyr Ala Glu Ser Val Lys 50 55 60Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr Leu65 70 75 80Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys Asp 85 90 95Ser Tyr Gly Tyr Arg Gly Gln Gly Thr Leu Val Thr Val Ser Ser 100 105 110132111PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 132Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser Arg Phe Met Ile Ser Pro Tyr 20 25 30Ser Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Thr Ile Asn Pro Ala Gly Thr Thr Asp Tyr Ala Glu Ser Val Lys 50 55 60Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr Leu65 70 75 80Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys Asp 85 90 95Gly Tyr Gly Tyr Arg Gly Gln Gly Thr Leu Val Thr Val Ser Ser 100 105 110133111PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 133Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser Arg Phe Met Ile Ser Glu Tyr 20 25 30Ser Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Thr Ile Asn Pro Ala Gly Gln Thr Asp Tyr Ala Glu Ser Val Lys 50 55 60Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr Leu65 70 75 80Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys Asp 85 90 95Gly Tyr Gly Tyr Arg Gly Gln Gly Thr Leu Val Thr Val Ser Ser 100 105 110134111PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 134Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser Arg Phe Met Ile Ser Glu Tyr 20 25 30Ser Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Thr Ile Asn Pro Ala Gly Thr Thr Asp Tyr Ala Glu Tyr Val Lys 50 55 60Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr Leu65 70 75 80Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys Asp 85 90 95Gly Tyr Gly Tyr Arg Gly Gln Gly Thr Leu Val Thr Val Ser Ser 100 105 110135111PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 135Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser Arg Phe Met Ile Ser Glu Tyr 20 25 30His Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Asp Ile Asn Pro Ala Lys Thr Thr Asp Tyr Ala Glu Ser Val Lys 50 55 60Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr Leu65 70 75 80Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys Asp 85 90 95Ser Tyr Gly Tyr Arg Gly Gln Gly Thr Leu Val Thr Val Ser Ser 100 105 110136111PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 136Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser Arg Phe Met Ile Ser Pro Tyr 20 25 30His Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Asp Ile Asn Pro Ala Gly Thr Thr Asp Tyr Ala Glu Ser Val Lys 50 55 60Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr Leu65 70 75 80Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys Asp 85 90 95Ser Tyr Gly Tyr Arg Gly Gln Gly Thr Leu Val Thr Val Ser Ser 100 105 110137111PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 137Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser Arg Phe Met Ile Ser Glu Tyr 20 25 30His Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Asp Ile Asn Pro Ala Gly Gln Thr Asp Tyr Ala Glu Ser Val Lys 50 55 60Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr Leu65 70 75 80Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys Asp 85 90 95Ser Tyr Gly Tyr Arg Gly Gln Gly Thr Leu Val Thr Val Ser Ser 100 105 110138111PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 138Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser Arg Phe Met Ile Ser Glu Tyr 20 25 30His Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Asp Ile Asn Pro Ala Gly Thr Thr Asp Tyr Ala Glu Tyr Val Lys 50 55 60Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr Leu65 70 75 80Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys Asp 85 90 95Ser Tyr Gly Tyr Arg Gly Gln Gly Thr Leu Val Thr Val Ser Ser 100 105 110139111PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 139Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Thr Leu Ser Cys Ala Ala Ser Arg Phe Met Ile Ser Glu Tyr 20 25 30His Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Asp Ile Asn Pro Ala Gly Thr Thr Asp Tyr Ala Glu Ser Val Lys 50 55 60Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr Leu65 70 75 80Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Tyr Cys Asp 85 90 95Ser Tyr Gly Tyr Arg Gly Gln Gly Thr Gln Val Thr Val Ser Ser 100 105 110140111PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 140Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Thr Leu Ser Cys Ala Ala Ser Arg Phe Met Ile Ser Glu Tyr 20 25 30His Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Thr Ile Asn Pro Ala Gly Thr Thr Asp Tyr Ala Glu Ser Val Lys 50 55 60Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr Leu65 70 75 80Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Tyr Cys Asp 85 90 95Ser Tyr Gly Tyr Arg Gly Gln Gly Thr Gln Val Thr Val Ser Ser 100 105 110141499PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 141Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Thr Leu Ser Cys Ala Ala Ser Arg Phe Met Ile Ser Glu Tyr 20 25 30Ser Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Thr Ile Asn Pro Ala Gly Thr Thr Asp Tyr Ala Glu Ser Val Lys 50 55 60Gly Arg

Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr Leu65 70 75 80Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Tyr Cys Asp 85 90 95Gly Tyr Gly Tyr Arg Gly Gln Gly Thr Gln Val Thr Val Ser Ser Gly 100 105 110Gly Gly Gly Ser Gly Gly Gly Ser Glu Val Gln Leu Val Glu Ser Gly 115 120 125Gly Gly Leu Val Gln Pro Gly Asn Ser Leu Arg Leu Ser Cys Ala Ala 130 135 140Ser Gly Phe Thr Phe Ser Lys Phe Gly Met Ser Trp Val Arg Gln Ala145 150 155 160Pro Gly Lys Gly Leu Glu Trp Val Ser Ser Ile Ser Gly Ser Gly Arg 165 170 175Asp Thr Leu Tyr Ala Asp Ser Val Lys Gly Arg Phe Thr Ile Ser Arg 180 185 190Asp Asn Ala Lys Thr Thr Leu Tyr Leu Gln Met Asn Ser Leu Arg Pro 195 200 205Glu Asp Thr Ala Val Tyr Tyr Cys Thr Ile Gly Gly Ser Leu Ser Val 210 215 220Ser Ser Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly Gly Ser225 230 235 240Gly Gly Gly Ser Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val 245 250 255Gln Pro Gly Gly Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Thr 260 265 270Phe Asn Lys Tyr Ala Ile Asn Trp Val Arg Gln Ala Pro Gly Lys Gly 275 280 285Leu Glu Trp Val Ala Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Ala Thr 290 295 300Tyr Tyr Ala Asp Gln Val Lys Asp Arg Phe Thr Ile Ser Arg Asp Asp305 310 315 320Ser Lys Asn Thr Ala Tyr Leu Gln Met Asn Asn Leu Lys Thr Glu Asp 325 330 335Thr Ala Val Tyr Tyr Cys Val Arg His Ala Asn Phe Gly Asn Ser Tyr 340 345 350Ile Ser Tyr Trp Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser 355 360 365Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser 370 375 380Gln Thr Val Val Thr Gln Glu Pro Ser Leu Thr Val Ser Pro Gly Gly385 390 395 400Thr Val Thr Leu Thr Cys Ala Ser Ser Thr Gly Ala Val Thr Ser Gly 405 410 415Asn Tyr Pro Asn Trp Val Gln Gln Lys Pro Gly Gln Ala Pro Arg Gly 420 425 430Leu Ile Gly Gly Thr Lys Phe Leu Val Pro Gly Thr Pro Ala Arg Phe 435 440 445Ser Gly Ser Leu Leu Gly Gly Lys Ala Ala Leu Thr Leu Ser Gly Val 450 455 460Gln Pro Glu Asp Glu Ala Glu Tyr Tyr Cys Thr Leu Trp Tyr Ser Asn465 470 475 480Arg Trp Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu His His His 485 490 495His His His142499PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 142Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Thr Leu Ser Cys Ala Ala Ser Arg Phe Met Ile Ser Glu Tyr 20 25 30Ser Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Thr Ile Asn Pro Ala Gly Thr Thr Asp Tyr Ala Glu Ser Val Lys 50 55 60Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr Leu65 70 75 80Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Tyr Cys Asp 85 90 95Gly Tyr Gly Tyr Arg Gly Gln Gly Thr Gln Val Thr Val Ser Ser Gly 100 105 110Gly Gly Gly Ser Gly Gly Gly Ser Glu Val Gln Leu Val Glu Ser Gly 115 120 125Gly Gly Leu Val Gln Pro Gly Asn Ser Leu Arg Leu Ser Cys Ala Ala 130 135 140Ser Gly Phe Thr Phe Ser Lys Phe Gly Met Ser Trp Val Arg Gln Ala145 150 155 160Pro Gly Lys Gly Leu Glu Trp Val Ser Ser Ile Ser Gly Ser Gly Arg 165 170 175Asp Thr Leu Tyr Ala Asp Ser Val Lys Gly Arg Phe Thr Ile Ser Arg 180 185 190Asp Asn Ala Lys Thr Thr Leu Tyr Leu Gln Met Asn Ser Leu Arg Pro 195 200 205Glu Asp Thr Ala Val Tyr Tyr Cys Thr Ile Gly Gly Ser Leu Ser Val 210 215 220Ser Ser Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly Gly Ser225 230 235 240Gly Gly Gly Ser Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val 245 250 255Gln Pro Gly Gly Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Thr 260 265 270Phe Asn Asn Tyr Ala Met Asn Trp Val Arg Gln Ala Pro Gly Lys Gly 275 280 285Leu Glu Trp Val Ala Arg Ile Arg Ser Gly Tyr Asn Asn Tyr Ala Thr 290 295 300Tyr Tyr Ala Asp Ser Val Lys Asp Arg Phe Thr Ile Ser Arg Asp Asp305 310 315 320Ser Lys Asn Thr Ala Tyr Leu Gln Met Asn Asn Leu Lys Thr Glu Asp 325 330 335Thr Ala Val Tyr Tyr Cys Val Arg His Gly Asn Phe Gly Asn Ser Tyr 340 345 350Ile Ser Tyr Trp Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser 355 360 365Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser 370 375 380Gln Thr Val Val Thr Gln Glu Pro Ser Leu Thr Val Ser Pro Gly Gly385 390 395 400Thr Val Thr Leu Thr Cys Gly Ser Tyr Thr Gly Ala Val Thr Ser Gly 405 410 415Asn Tyr Pro Asn Trp Val Gln Gln Lys Pro Gly Gln Ala Pro Arg Gly 420 425 430Leu Ile Gly Gly Thr Lys Phe Asn Ala Pro Gly Thr Pro Ala Arg Phe 435 440 445Ser Gly Ser Leu Leu Gly Gly Lys Ala Ala Leu Thr Leu Ser Gly Val 450 455 460Gln Pro Glu Asp Glu Ala Glu Tyr Tyr Cys Val Leu Trp Tyr Ala Asn465 470 475 480Arg Trp Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu His His His 485 490 495His His His143499PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 143Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Thr Leu Ser Cys Ala Ala Ser Arg Phe Met Ile Ser Glu Tyr 20 25 30Ser Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Thr Ile Asn Pro Ala Gly Thr Thr Asp Tyr Ala Glu Ser Val Lys 50 55 60Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr Leu65 70 75 80Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Tyr Cys Asp 85 90 95Gly Tyr Gly Tyr Arg Gly Gln Gly Thr Gln Val Thr Val Ser Ser Gly 100 105 110Gly Gly Gly Ser Gly Gly Gly Ser Glu Val Gln Leu Val Glu Ser Gly 115 120 125Gly Gly Leu Val Gln Pro Gly Asn Ser Leu Arg Leu Ser Cys Ala Ala 130 135 140Ser Gly Phe Thr Phe Ser Lys Phe Gly Met Ser Trp Val Arg Gln Ala145 150 155 160Pro Gly Lys Gly Leu Glu Trp Val Ser Ser Ile Ser Gly Ser Gly Arg 165 170 175Asp Thr Leu Tyr Ala Asp Ser Val Lys Gly Arg Phe Thr Ile Ser Arg 180 185 190Asp Asn Ala Lys Thr Thr Leu Tyr Leu Gln Met Asn Ser Leu Arg Pro 195 200 205Glu Asp Thr Ala Val Tyr Tyr Cys Thr Ile Gly Gly Ser Leu Ser Val 210 215 220Ser Ser Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly Gly Ser225 230 235 240Gly Gly Gly Ser Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val 245 250 255Gln Pro Gly Gly Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Glu 260 265 270Phe Asn Lys Tyr Ala Met Asn Trp Val Arg Gln Ala Pro Gly Lys Gly 275 280 285Leu Glu Trp Val Ala Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Glu Thr 290 295 300Tyr Tyr Ala Asp Ser Val Lys Asp Arg Phe Thr Ile Ser Arg Asp Asp305 310 315 320Ser Lys Asn Thr Ala Tyr Leu Gln Met Asn Asn Leu Lys Thr Glu Asp 325 330 335Thr Ala Val Tyr Tyr Cys Val Arg His Gly Asn Phe Gly Asn Ser Leu 340 345 350Ile Ser Tyr Trp Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser 355 360 365Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser 370 375 380Gln Thr Val Val Thr Gln Glu Pro Ser Leu Thr Val Ser Pro Gly Gly385 390 395 400Thr Val Thr Leu Thr Cys Gly Ser Ser Ser Gly Ala Val Thr Ser Gly 405 410 415Asn Tyr Pro Asn Trp Val Gln Gln Lys Pro Gly Gln Ala Pro Arg Gly 420 425 430Leu Ile Gly Gly Thr Lys Phe Gly Ala Pro Gly Thr Pro Ala Arg Phe 435 440 445Ser Gly Ser Leu Leu Gly Gly Lys Ala Ala Leu Thr Leu Ser Gly Val 450 455 460Gln Pro Glu Asp Glu Ala Glu Tyr Tyr Cys Val Leu Trp Tyr Ser Asn465 470 475 480Arg Trp Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu His His His 485 490 495His His His144499PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 144Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Thr Leu Ser Cys Ala Ala Ser Arg Phe Met Ile Ser Glu Tyr 20 25 30Ser Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Thr Ile Asn Pro Ala Gly Thr Thr Asp Tyr Ala Glu Ser Val Lys 50 55 60Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr Leu65 70 75 80Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Tyr Cys Asp 85 90 95Gly Tyr Gly Tyr Arg Gly Gln Gly Thr Gln Val Thr Val Ser Ser Gly 100 105 110Gly Gly Gly Ser Gly Gly Gly Ser Glu Val Gln Leu Val Glu Ser Gly 115 120 125Gly Gly Leu Val Gln Pro Gly Asn Ser Leu Arg Leu Ser Cys Ala Ala 130 135 140Ser Gly Phe Thr Phe Ser Ser Phe Gly Met Ser Trp Val Arg Gln Ala145 150 155 160Pro Gly Lys Gly Leu Glu Trp Val Ser Ser Ile Ser Gly Ser Gly Ser 165 170 175Asp Thr Leu Tyr Ala Asp Ser Val Lys Gly Arg Phe Thr Ile Ser Arg 180 185 190Asp Asn Ala Lys Thr Thr Leu Tyr Leu Gln Met Asn Ser Leu Arg Pro 195 200 205Glu Asp Thr Ala Val Tyr Tyr Cys Thr Ile Gly Gly Ser Leu Ser Arg 210 215 220Ser Ser Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly Gly Ser225 230 235 240Gly Gly Gly Ser Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val 245 250 255Gln Pro Gly Gly Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Thr 260 265 270Phe Asn Lys Tyr Ala Met Asn Trp Val Arg Gln Ala Pro Gly Lys Gly 275 280 285Leu Glu Trp Val Ala Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Ala Thr 290 295 300Tyr Tyr Ala Asp Ser Val Lys Asp Arg Phe Thr Ile Ser Arg Asp Asp305 310 315 320Ser Lys Asn Thr Ala Tyr Leu Gln Met Asn Asn Leu Lys Thr Glu Asp 325 330 335Thr Ala Val Tyr Tyr Cys Val Arg His Gly Asn Phe Gly Asn Ser Tyr 340 345 350Ile Ser Tyr Trp Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser 355 360 365Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser 370 375 380Gln Thr Val Val Thr Gln Glu Pro Ser Leu Thr Val Ser Pro Gly Gly385 390 395 400Thr Val Thr Leu Thr Cys Gly Ser Ser Thr Gly Ala Val Thr Ser Gly 405 410 415Asn Tyr Pro Asn Trp Val Gln Gln Lys Pro Gly Gln Ala Pro Arg Gly 420 425 430Leu Ile Gly Gly Thr Lys Phe Leu Ala Pro Gly Thr Pro Ala Arg Phe 435 440 445Ser Gly Ser Leu Leu Gly Gly Lys Ala Ala Leu Thr Leu Ser Gly Val 450 455 460Gln Pro Glu Asp Glu Ala Glu Tyr Tyr Cys Val Leu Trp Tyr Ser Asn465 470 475 480Arg Trp Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu His His His 485 490 495His His His145499PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 145Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser Arg Phe Met Ile Ser Glu Tyr 20 25 30Ser Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Thr Ile Asn Pro Ala Gly Thr Thr Asp Tyr Ala Glu Ser Val Lys 50 55 60Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr Leu65 70 75 80Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys Asp 85 90 95Gly Tyr Gly Tyr Arg Gly Gln Gly Thr Leu Val Thr Val Ser Ser Gly 100 105 110Gly Gly Gly Ser Gly Gly Gly Ser Glu Val Gln Leu Val Glu Ser Gly 115 120 125Gly Gly Leu Val Gln Pro Gly Asn Ser Leu Arg Leu Ser Cys Ala Ala 130 135 140Ser Gly Phe Thr Phe Ser Lys Phe Gly Met Ser Trp Val Arg Gln Ala145 150 155 160Pro Gly Lys Gly Leu Glu Trp Val Ser Ser Ile Ser Gly Ser Gly Arg 165 170 175Asp Thr Leu Tyr Ala Asp Ser Val Lys Gly Arg Phe Thr Ile Ser Arg 180 185 190Asp Asn Ala Lys Thr Thr Leu Tyr Leu Gln Met Asn Ser Leu Arg Pro 195 200 205Glu Asp Thr Ala Val Tyr Tyr Cys Thr Ile Gly Gly Ser Leu Ser Val 210 215 220Ser Ser Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly Gly Ser225 230 235 240Gly Gly Gly Ser Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val 245 250 255Gln Pro Gly Gly Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Thr 260 265 270Phe Asn Lys Tyr Ala Ile Asn Trp Val Arg Gln Ala Pro Gly Lys Gly 275 280 285Leu Glu Trp Val Ala Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Ala Thr 290 295 300Tyr Tyr Ala Asp Gln Val Lys Asp Arg Phe Thr Ile Ser Arg Asp Asp305 310 315 320Ser Lys Asn Thr Ala Tyr Leu Gln Met Asn Asn Leu Lys Thr Glu Asp 325 330 335Thr Ala Val Tyr Tyr Cys Val Arg His Ala Asn Phe Gly Asn Ser Tyr 340 345 350Ile Ser Tyr Trp Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser 355 360 365Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser 370 375 380Gln Thr Val Val Thr Gln Glu Pro Ser Leu Thr Val Ser Pro Gly Gly385 390 395 400Thr Val Thr Leu Thr Cys Ala Ser Ser Thr Gly Ala Val Thr Ser Gly 405 410 415Asn Tyr Pro Asn Trp Val Gln Gln Lys Pro Gly Gln Ala Pro Arg Gly 420 425 430Leu Ile Gly Gly Thr Lys Phe Leu Val Pro Gly Thr Pro Ala Arg Phe 435 440 445Ser Gly Ser Leu Leu Gly Gly Lys Ala Ala Leu Thr Leu Ser Gly Val 450 455 460Gln Pro Glu Asp Glu Ala Glu Tyr Tyr Cys Thr Leu Trp Tyr Ser Asn465 470 475 480Arg Trp Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu His His His

485 490 495His His His146499PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 146Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Thr Leu Ser Cys Ala Ala Ser Arg Phe Met Ile Ser Glu Tyr 20 25 30His Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Asp Ile Asn Pro Ala Gly Thr Thr Asp Tyr Ala Glu Ser Val Lys 50 55 60Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr Leu65 70 75 80Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Tyr Cys Asp 85 90 95Ser Tyr Gly Tyr Arg Gly Gln Gly Thr Gln Val Thr Val Ser Ser Gly 100 105 110Gly Gly Gly Ser Gly Gly Gly Ser Glu Val Gln Leu Val Glu Ser Gly 115 120 125Gly Gly Leu Val Gln Pro Gly Asn Ser Leu Arg Leu Ser Cys Ala Ala 130 135 140Ser Gly Phe Thr Phe Ser Lys Phe Gly Met Ser Trp Val Arg Gln Ala145 150 155 160Pro Gly Lys Gly Leu Glu Trp Val Ser Ser Ile Ser Gly Ser Gly Arg 165 170 175Asp Thr Leu Tyr Ala Asp Ser Val Lys Gly Arg Phe Thr Ile Ser Arg 180 185 190Asp Asn Ala Lys Thr Thr Leu Tyr Leu Gln Met Asn Ser Leu Arg Pro 195 200 205Glu Asp Thr Ala Val Tyr Tyr Cys Thr Ile Gly Gly Ser Leu Ser Val 210 215 220Ser Ser Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly Gly Ser225 230 235 240Gly Gly Gly Ser Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val 245 250 255Gln Pro Gly Gly Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Thr 260 265 270Phe Asn Lys Tyr Ala Ile Asn Trp Val Arg Gln Ala Pro Gly Lys Gly 275 280 285Leu Glu Trp Val Ala Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Ala Thr 290 295 300Tyr Tyr Ala Asp Gln Val Lys Asp Arg Phe Thr Ile Ser Arg Asp Asp305 310 315 320Ser Lys Asn Thr Ala Tyr Leu Gln Met Asn Asn Leu Lys Thr Glu Asp 325 330 335Thr Ala Val Tyr Tyr Cys Val Arg His Ala Asn Phe Gly Asn Ser Tyr 340 345 350Ile Ser Tyr Trp Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser 355 360 365Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser 370 375 380Gln Thr Val Val Thr Gln Glu Pro Ser Leu Thr Val Ser Pro Gly Gly385 390 395 400Thr Val Thr Leu Thr Cys Ala Ser Ser Thr Gly Ala Val Thr Ser Gly 405 410 415Asn Tyr Pro Asn Trp Val Gln Gln Lys Pro Gly Gln Ala Pro Arg Gly 420 425 430Leu Ile Gly Gly Thr Lys Phe Leu Val Pro Gly Thr Pro Ala Arg Phe 435 440 445Ser Gly Ser Leu Leu Gly Gly Lys Ala Ala Leu Thr Leu Ser Gly Val 450 455 460Gln Pro Glu Asp Glu Ala Glu Tyr Tyr Cys Thr Leu Trp Tyr Ser Asn465 470 475 480Arg Trp Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu His His His 485 490 495His His His147499PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 147Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Thr Leu Ser Cys Ala Ala Ser Arg Phe Met Ile Ser Glu Tyr 20 25 30His Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Thr Ile Asn Pro Ala Gly Thr Thr Asp Tyr Ala Glu Ser Val Lys 50 55 60Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr Leu65 70 75 80Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Tyr Cys Asp 85 90 95Ser Tyr Gly Tyr Arg Gly Gln Gly Thr Gln Val Thr Val Ser Ser Gly 100 105 110Gly Gly Gly Ser Gly Gly Gly Ser Glu Val Gln Leu Val Glu Ser Gly 115 120 125Gly Gly Leu Val Gln Pro Gly Asn Ser Leu Arg Leu Ser Cys Ala Ala 130 135 140Ser Gly Phe Thr Phe Ser Lys Phe Gly Met Ser Trp Val Arg Gln Ala145 150 155 160Pro Gly Lys Gly Leu Glu Trp Val Ser Ser Ile Ser Gly Ser Gly Arg 165 170 175Asp Thr Leu Tyr Ala Asp Ser Val Lys Gly Arg Phe Thr Ile Ser Arg 180 185 190Asp Asn Ala Lys Thr Thr Leu Tyr Leu Gln Met Asn Ser Leu Arg Pro 195 200 205Glu Asp Thr Ala Val Tyr Tyr Cys Thr Ile Gly Gly Ser Leu Ser Val 210 215 220Ser Ser Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly Gly Ser225 230 235 240Gly Gly Gly Ser Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val 245 250 255Gln Pro Gly Gly Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Thr 260 265 270Phe Asn Lys Tyr Ala Ile Asn Trp Val Arg Gln Ala Pro Gly Lys Gly 275 280 285Leu Glu Trp Val Ala Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Ala Thr 290 295 300Tyr Tyr Ala Asp Gln Val Lys Asp Arg Phe Thr Ile Ser Arg Asp Asp305 310 315 320Ser Lys Asn Thr Ala Tyr Leu Gln Met Asn Asn Leu Lys Thr Glu Asp 325 330 335Thr Ala Val Tyr Tyr Cys Val Arg His Ala Asn Phe Gly Asn Ser Tyr 340 345 350Ile Ser Tyr Trp Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser 355 360 365Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser 370 375 380Gln Thr Val Val Thr Gln Glu Pro Ser Leu Thr Val Ser Pro Gly Gly385 390 395 400Thr Val Thr Leu Thr Cys Ala Ser Ser Thr Gly Ala Val Thr Ser Gly 405 410 415Asn Tyr Pro Asn Trp Val Gln Gln Lys Pro Gly Gln Ala Pro Arg Gly 420 425 430Leu Ile Gly Gly Thr Lys Phe Leu Val Pro Gly Thr Pro Ala Arg Phe 435 440 445Ser Gly Ser Leu Leu Gly Gly Lys Ala Ala Leu Thr Leu Ser Gly Val 450 455 460Gln Pro Glu Asp Glu Ala Glu Tyr Tyr Cys Thr Leu Trp Tyr Ser Asn465 470 475 480Arg Trp Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu His His His 485 490 495His His His148504PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 148Gln Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Lys Pro Gly Glu1 5 10 15Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Asp Tyr 20 25 30Tyr Met Tyr Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ala Ile Ile Ser Asp Gly Gly Tyr Tyr Thr Tyr Tyr Ser Asp Ile Ile 50 55 60Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Ser Leu Tyr65 70 75 80Leu Gln Met Asn Ser Leu Lys Ala Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala Arg Gly Phe Pro Leu Leu Arg His Gly Ala Met Asp Tyr Trp Gly 100 105 110Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly Gly Ser Gly Gly 115 120 125Gly Gly Ser Gly Gly Gly Gly Ser Asp Ile Gln Met Thr Gln Ser Pro 130 135 140Ser Ser Leu Ser Ala Ser Val Gly Asp Arg Val Thr Ile Thr Cys Lys145 150 155 160Ala Ser Gln Asn Val Asp Thr Asn Val Ala Trp Tyr Gln Gln Lys Pro 165 170 175Gly Gln Ala Pro Lys Ser Leu Ile Tyr Ser Ala Ser Tyr Arg Tyr Ser 180 185 190Asp Val Pro Ser Arg Phe Ser Gly Ser Ala Ser Gly Thr Asp Phe Thr 195 200 205Leu Thr Ile Ser Ser Val Gln Ser Glu Asp Phe Ala Thr Tyr Tyr Cys 210 215 220Gln Gln Tyr Asp Ser Tyr Pro Tyr Thr Phe Gly Gly Gly Thr Lys Leu225 230 235 240Glu Ile Lys Ser Gly Gly Gly Gly Ser Glu Val Gln Leu Val Glu Ser 245 250 255Gly Gly Gly Leu Val Gln Pro Gly Gly Ser Leu Lys Leu Ser Cys Ala 260 265 270Ala Ser Gly Phe Thr Phe Asn Lys Tyr Ala Met Asn Trp Val Arg Gln 275 280 285Ala Pro Gly Lys Gly Leu Glu Trp Val Ala Arg Ile Arg Ser Lys Tyr 290 295 300Asn Asn Tyr Ala Thr Tyr Tyr Ala Asp Ser Val Lys Asp Arg Phe Thr305 310 315 320Ile Ser Arg Asp Asp Ser Lys Asn Thr Ala Tyr Leu Gln Met Asn Asn 325 330 335Leu Lys Thr Glu Asp Thr Ala Val Tyr Tyr Cys Val Arg His Gly Asn 340 345 350Phe Gly Asn Ser Tyr Ile Ser Tyr Trp Ala Tyr Trp Gly Gln Gly Thr 355 360 365Leu Val Thr Val Ser Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser 370 375 380Gly Gly Gly Gly Ser Gln Thr Val Val Thr Gln Glu Pro Ser Leu Thr385 390 395 400Val Ser Pro Gly Gly Thr Val Thr Leu Thr Cys Gly Ser Ser Thr Gly 405 410 415Ala Val Thr Ser Gly Asn Tyr Pro Asn Trp Val Gln Gln Lys Pro Gly 420 425 430Gln Ala Pro Arg Gly Leu Ile Gly Gly Thr Lys Phe Leu Ala Pro Gly 435 440 445Thr Pro Ala Arg Phe Ser Gly Ser Leu Leu Gly Gly Lys Ala Ala Leu 450 455 460Thr Leu Ser Gly Val Gln Pro Glu Asp Glu Ala Glu Tyr Tyr Cys Val465 470 475 480Leu Trp Tyr Ser Asn Arg Trp Val Phe Gly Gly Gly Thr Lys Leu Thr 485 490 495Val Leu His His His His His His 500149512PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 149Gln Val Lys Leu Glu Glu Ser Gly Gly Gly Ser Val Gln Thr Gly Gly1 5 10 15Ser Leu Arg Leu Thr Cys Ala Ala Ser Gly Arg Thr Ser Arg Ser Tyr 20 25 30Gly Met Gly Trp Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu Phe Val 35 40 45Ser Gly Ile Ser Trp Arg Gly Asp Ser Thr Gly Tyr Ala Asp Ser Val 50 55 60Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Val Asp65 70 75 80Leu Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Ile Tyr Tyr Cys 85 90 95Ala Ala Ala Ala Gly Ser Ala Trp Tyr Gly Thr Leu Tyr Glu Tyr Asp 100 105 110Tyr Trp Gly Gln Gly Thr Gln Val Thr Val Ser Ser Gly Gly Gly Gly 115 120 125Ser Gly Gly Gly Ser Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu 130 135 140Val Gln Pro Gly Asn Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe145 150 155 160Thr Phe Ser Ser Phe Gly Met Ser Trp Val Arg Gln Ala Pro Gly Lys 165 170 175Gly Leu Glu Trp Val Ser Ser Ile Ser Gly Ser Gly Ser Asp Thr Leu 180 185 190Tyr Ala Asp Ser Val Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala 195 200 205Lys Thr Thr Leu Tyr Leu Gln Met Asn Ser Leu Arg Pro Glu Asp Thr 210 215 220Ala Val Tyr Tyr Cys Thr Ile Gly Gly Ser Leu Ser Arg Ser Ser Gln225 230 235 240Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly Gly Ser Gly Gly Gly 245 250 255Ser Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly 260 265 270Gly Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Asn Lys 275 280 285Tyr Ala Met Asn Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp 290 295 300Val Ala Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Ala Thr Tyr Tyr Ala305 310 315 320Asp Ser Val Lys Asp Arg Phe Thr Ile Ser Arg Asp Asp Ser Lys Asn 325 330 335Thr Ala Tyr Leu Gln Met Asn Asn Leu Lys Thr Glu Asp Thr Ala Val 340 345 350Tyr Tyr Cys Val Arg His Gly Asn Phe Gly Asn Ser Tyr Ile Ser Tyr 355 360 365Trp Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly 370 375 380Gly Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gln Thr Val385 390 395 400Val Thr Gln Glu Pro Ser Leu Thr Val Ser Pro Gly Gly Thr Val Thr 405 410 415Leu Thr Cys Gly Ser Ser Thr Gly Ala Val Thr Ser Gly Asn Tyr Pro 420 425 430Asn Trp Val Gln Gln Lys Pro Gly Gln Ala Pro Arg Gly Leu Ile Gly 435 440 445Gly Thr Lys Phe Leu Ala Pro Gly Thr Pro Ala Arg Phe Ser Gly Ser 450 455 460Leu Leu Gly Gly Lys Ala Ala Leu Thr Leu Ser Gly Val Gln Pro Glu465 470 475 480Asp Glu Ala Glu Tyr Tyr Cys Val Leu Trp Tyr Ser Asn Arg Trp Val 485 490 495Phe Gly Gly Gly Thr Lys Leu Thr Val Leu His His His His His His 500 505 510150508PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 150Gln Val Gln Leu Val Glu Ser Gly Gly Gly Val Val Gln Ala Gly Arg1 5 10 15Ser Leu Thr Leu Ser Cys Ala Tyr Ser Gly Val Thr Val Asn Val Tyr 20 25 30Arg Met Gly Trp Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu Phe Val 35 40 45Ala Asn Ile Asn Trp Ser Gly Asn Asn Arg Asp Tyr Ala Asp Ser Val 50 55 60Arg Gly Arg Phe Thr Ile Ser Arg Asp Asn Ser Lys Asn Thr Leu Tyr65 70 75 80Leu Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala Ser Glu Lys Pro Gly Arg Leu Gly Glu Tyr Asp Tyr Gly Ser Gln 100 105 110Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly Gly Ser Gly Gly Gly 115 120 125Ser Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly 130 135 140Asn Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Lys145 150 155 160Phe Gly Met Ser Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp 165 170 175Val Ser Ser Ile Ser Gly Ser Gly Arg Asp Thr Leu Tyr Ala Asp Ser 180 185 190Val Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Thr Thr Leu 195 200 205Tyr Leu Gln Met Asn Ser Leu Arg Pro Glu Asp Thr Ala Val Tyr Tyr 210 215 220Cys Thr Ile Gly Gly Ser Leu Ser Val Ser Ser Gln Gly Thr Leu Val225 230 235 240Thr Val Ser Ser Gly Gly Gly Gly Ser Gly Gly Gly Ser Glu Val Gln 245 250 255Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly Ser Leu Lys 260 265 270Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Asn Lys Tyr Ala Ile Asn 275 280 285Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val Ala Arg Ile 290 295 300Arg Ser Lys Tyr Asn Asn Tyr Ala Thr Tyr Tyr Ala Asp Gln Val Lys305 310 315 320Asp Arg Phe Thr Ile Ser Arg Asp Asp Ser Lys Asn Thr Ala Tyr Leu 325 330 335Gln Met Asn Asn Leu Lys Thr Glu Asp Thr Ala Val Tyr Tyr Cys Val 340 345 350Arg His Ala Asn Phe Gly Asn Ser Tyr Ile Ser Tyr Trp Ala Tyr Trp 355 360 365Gly Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly Gly Ser Gly 370 375 380Gly Gly Gly Ser Gly

Gly Gly Gly Ser Gln Thr Val Val Thr Gln Glu385 390 395 400Pro Ser Leu Thr Val Ser Pro Gly Gly Thr Val Thr Leu Thr Cys Ala 405 410 415Ser Ser Thr Gly Ala Val Thr Ser Gly Asn Tyr Pro Asn Trp Val Gln 420 425 430Gln Lys Pro Gly Gln Ala Pro Arg Gly Leu Ile Gly Gly Thr Lys Phe 435 440 445Leu Val Pro Gly Thr Pro Ala Arg Phe Ser Gly Ser Leu Leu Gly Gly 450 455 460Lys Ala Ala Leu Thr Leu Ser Gly Val Gln Pro Glu Asp Glu Ala Glu465 470 475 480Tyr Tyr Cys Thr Leu Trp Tyr Ser Asn Arg Trp Val Phe Gly Gly Gly 485 490 495Thr Lys Leu Thr Val Leu His His His His His His 500 505151508PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 151Gln Val Gln Leu Val Glu Ser Gly Gly Gly Val Val Gln Ala Gly Arg1 5 10 15Ser Leu Arg Leu Ser Cys Ala Tyr Ser Gly Val Thr Val Asn Val Tyr 20 25 30Arg Met Gly Trp Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu Phe Val 35 40 45Ala Asn Ile Asn Trp Ser Gly Asn Asn Arg Asp Tyr Ala Asp Ser Val 50 55 60Arg Gly Arg Phe Thr Ile Ser Arg Asp Asn Ser Lys Asn Thr Leu Tyr65 70 75 80Leu Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys 85 90 95Ala Ser Glu Lys Pro Gly Arg Leu Gly Glu Tyr Asp Tyr Gly Ser Gln 100 105 110Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly Gly Ser Gly Gly Gly 115 120 125Ser Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly 130 135 140Asn Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Lys145 150 155 160Phe Gly Met Ser Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp 165 170 175Val Ser Ser Ile Ser Gly Ser Gly Arg Asp Thr Leu Tyr Ala Asp Ser 180 185 190Val Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Thr Thr Leu 195 200 205Tyr Leu Gln Met Asn Ser Leu Arg Pro Glu Asp Thr Ala Val Tyr Tyr 210 215 220Cys Thr Ile Gly Gly Ser Leu Ser Val Ser Ser Gln Gly Thr Leu Val225 230 235 240Thr Val Ser Ser Gly Gly Gly Gly Ser Gly Gly Gly Ser Glu Val Gln 245 250 255Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly Ser Leu Lys 260 265 270Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Asn Lys Tyr Ala Ile Asn 275 280 285Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val Ala Arg Ile 290 295 300Arg Ser Lys Tyr Asn Asn Tyr Ala Thr Tyr Tyr Ala Asp Gln Val Lys305 310 315 320Asp Arg Phe Thr Ile Ser Arg Asp Asp Ser Lys Asn Thr Ala Tyr Leu 325 330 335Gln Met Asn Asn Leu Lys Thr Glu Asp Thr Ala Val Tyr Tyr Cys Val 340 345 350Arg His Ala Asn Phe Gly Asn Ser Tyr Ile Ser Tyr Trp Ala Tyr Trp 355 360 365Gly Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly Gly Ser Gly 370 375 380Gly Gly Gly Ser Gly Gly Gly Gly Ser Gln Thr Val Val Thr Gln Glu385 390 395 400Pro Ser Leu Thr Val Ser Pro Gly Gly Thr Val Thr Leu Thr Cys Ala 405 410 415Ser Ser Thr Gly Ala Val Thr Ser Gly Asn Tyr Pro Asn Trp Val Gln 420 425 430Gln Lys Pro Gly Gln Ala Pro Arg Gly Leu Ile Gly Gly Thr Lys Phe 435 440 445Leu Val Pro Gly Thr Pro Ala Arg Phe Ser Gly Ser Leu Leu Gly Gly 450 455 460Lys Ala Ala Leu Thr Leu Ser Gly Val Gln Pro Glu Asp Glu Ala Glu465 470 475 480Tyr Tyr Cys Thr Leu Trp Tyr Ser Asn Arg Trp Val Phe Gly Gly Gly 485 490 495Thr Lys Leu Thr Val Leu His His His His His His 500 505152499PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 152Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Thr Leu Ser Cys Ala Ala Ser Arg Phe Met Ile Ser Glu Tyr 20 25 30His Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45Ser Thr Ile Asn Pro Ala Gly Thr Thr Asp Tyr Ala Glu Ser Val Lys 50 55 60Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr Leu65 70 75 80Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys Asp 85 90 95Ser Tyr Gly Tyr Arg Gly Gln Gly Thr Leu Val Thr Val Ser Ser Gly 100 105 110Gly Gly Gly Ser Gly Gly Gly Ser Glu Val Gln Leu Val Glu Ser Gly 115 120 125Gly Gly Leu Val Gln Pro Gly Asn Ser Leu Arg Leu Ser Cys Ala Ala 130 135 140Ser Gly Phe Thr Phe Ser Lys Phe Gly Met Ser Trp Val Arg Gln Ala145 150 155 160Pro Gly Lys Gly Leu Glu Trp Val Ser Ser Ile Ser Gly Ser Gly Arg 165 170 175Asp Thr Leu Tyr Ala Asp Ser Val Lys Gly Arg Phe Thr Ile Ser Arg 180 185 190Asp Asn Ala Lys Thr Thr Leu Tyr Leu Gln Met Asn Ser Leu Arg Pro 195 200 205Glu Asp Thr Ala Val Tyr Tyr Cys Thr Ile Gly Gly Ser Leu Ser Val 210 215 220Ser Ser Gln Gly Thr Leu Val Thr Val Ser Ser Gly Gly Gly Gly Ser225 230 235 240Gly Gly Gly Ser Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val 245 250 255Gln Pro Gly Gly Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Phe Thr 260 265 270Phe Asn Lys Tyr Ala Ile Asn Trp Val Arg Gln Ala Pro Gly Lys Gly 275 280 285Leu Glu Trp Val Ala Arg Ile Arg Ser Lys Tyr Asn Asn Tyr Ala Thr 290 295 300Tyr Tyr Ala Asp Gln Val Lys Asp Arg Phe Thr Ile Ser Arg Asp Asp305 310 315 320Ser Lys Asn Thr Ala Tyr Leu Gln Met Asn Asn Leu Lys Thr Glu Asp 325 330 335Thr Ala Val Tyr Tyr Cys Val Arg His Ala Asn Phe Gly Asn Ser Tyr 340 345 350Ile Ser Tyr Trp Ala Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser 355 360 365Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser 370 375 380Gln Thr Val Val Thr Gln Glu Pro Ser Leu Thr Val Ser Pro Gly Gly385 390 395 400Thr Val Thr Leu Thr Cys Ala Ser Ser Thr Gly Ala Val Thr Ser Gly 405 410 415Asn Tyr Pro Asn Trp Val Gln Gln Lys Pro Gly Gln Ala Pro Arg Gly 420 425 430Leu Ile Gly Gly Thr Lys Phe Leu Val Pro Gly Thr Pro Ala Arg Phe 435 440 445Ser Gly Ser Leu Leu Gly Gly Lys Ala Ala Leu Thr Leu Ser Gly Val 450 455 460Gln Pro Glu Asp Glu Ala Glu Tyr Tyr Cys Thr Leu Trp Tyr Ser Asn465 470 475 480Arg Trp Val Phe Gly Gly Gly Thr Lys Leu Thr Val Leu His His His 485 490 495His His His15320PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptideMISC_FEATURE(1)..(20)This sequence may encompass 1-10 "Gly Ser" repeating units 153Gly Ser Gly Ser Gly Ser Gly Ser Gly Ser Gly Ser Gly Ser Gly Ser1 5 10 15Gly Ser Gly Ser 2015430PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptideMISC_FEATURE(1)..(30)This sequence may encompass 1-10 "Gly Gly Ser" repeating units 154Gly Gly Ser Gly Gly Ser Gly Gly Ser Gly Gly Ser Gly Gly Ser Gly1 5 10 15Gly Ser Gly Gly Ser Gly Gly Ser Gly Gly Ser Gly Gly Ser 20 25 3015540PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptideMISC_FEATURE(1)..(40)This sequence may encompass 1-10 "Gly Gly Gly Ser" repeating units 155Gly Gly Gly Ser Gly Gly Gly Ser Gly Gly Gly Ser Gly Gly Gly Ser1 5 10 15Gly Gly Gly Ser Gly Gly Gly Ser Gly Gly Gly Ser Gly Gly Gly Ser 20 25 30Gly Gly Gly Ser Gly Gly Gly Ser 35 4015640PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptideMISC_FEATURE(1)..(40)This sequence may encompass 1-10 "Gly Gly Ser Gly" repeating units 156Gly Gly Ser Gly Gly Gly Ser Gly Gly Gly Ser Gly Gly Gly Ser Gly1 5 10 15Gly Gly Ser Gly Gly Gly Ser Gly Gly Gly Ser Gly Gly Gly Ser Gly 20 25 30Gly Gly Ser Gly Gly Gly Ser Gly 35 4015750PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptideMISC_FEATURE(1)..(50)This sequence may encompass 1-10 "Gly Gly Ser Gly Gly" repeating units 157Gly Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly1 5 10 15Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly 20 25 30Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser 35 40 45Gly Gly 5015850PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptideMISC_FEATURE(1)..(50)This sequence may encompass 1-10 "Gly Gly Gly Gly Ser" repeating units 158Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gly1 5 10 15Gly Gly Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gly Gly 20 25 30Gly Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly 35 40 45Gly Ser 5015920PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 159Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gly1 5 10 15Gly Gly Gly Ser 2016015PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 160Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser1 5 10 151616PRTArtificial SequenceDescription of Artificial Sequence Synthetic 6xHis tag 161His His His His His His1 516210PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptideMOD_RES(6)..(6)Glu, Pro, Ser, His, Thr, Asp, Gly, Lys, Gln or TyrMOD_RES(8)..(8)Glu, Pro, Ser, His, Thr, Asp, Gly, Lys, Gln or Tyr 162Arg Phe Met Ile Ser Xaa Tyr Xaa Met His1 5 1016316PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptideMOD_RES(1)..(1)Glu, Pro, Ser, His, Thr, Asp, Gly, Lys, Gln or TyrMOD_RES(6)..(7)Glu, Pro, Ser, His, Thr, Asp, Gly, Lys, Gln or TyrMOD_RES(13)..(13)Glu, Pro, Ser, His, Thr, Asp, Gly, Lys, Gln or Tyr 163Xaa Ile Asn Pro Ala Xaa Xaa Thr Asp Tyr Ala Glu Xaa Val Lys Gly1 5 10 151645PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptideMOD_RES(2)..(2)Glu, Pro, Ser, His, Thr, Asp, Gly, Lys, Gln or Tyr 164Asp Xaa Tyr Gly Tyr1 516525PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 165Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly1 5 10 15Ser Leu Thr Leu Ser Cys Ala Ala Ser 20 2516614PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 166Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val Ser1 5 1016730PRTArtificial SequenceDescription of Artificial Sequence Synthetic polypeptide 167Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Leu Tyr Leu Gln1 5 10 15Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys 20 25 3016816PRTArtificial SequenceDescription of Artificial Sequence Synthetic peptide 168Asp Gly Tyr Gly Tyr Arg Gly Gln Gly Thr Leu Val Thr Val Ser Ser1 5 10 15

Claims

1. A trispecific protein targeting an epitope within a human prostate specific membrane antigen (PSMA), wherein said protein comprises (a) a first domain (A) which is a single chain variable fragment (scFv) that specifically binds to a human CD3, comprising a heavy chain complementarity determining region (HC CDR) 1, a HC CDR2, a HC CDR3, a light chain complementarity determining region (LC CDR) 1, a LC CDR 2, and a LC CDR 3, wherein the HC CDR1 comprises the amino acid sequence of SEQ ID NO: 32; the HC CDR2 comprises the amino acid sequence of SEQ ID NO: 42; the HC CDR3 comprises the amino acid sequence of SEQ ID NO: 44, the LC CDR1 comprises the amino acid sequence of SEQ ID NO: 54; the LC CDR2 comprises the amino acid sequence of SEQ ID NO: 79; and the LC CDR3 comprises the amino acid sequence of SEQ ID NO: 80; (b) a second domain (B) which is a single domain antibody (sdAb) comprising a CDR1, a CDR2 and a CDR3, wherein the CDR1 comprises the amino acid sequence of SEQ ID NO: 100; the CDR2 comprises the amino acid sequence of SEQ ID NO: 104; and the CDR3 comprises the amino acid sequence of SEQ ID NO: 109; and (c) a third domain (C) which is a sdAb that specifically binds to the human PSMA, comprising a CDR1, a CDR2, and a CDR3, wherein the CDR1 comprises the amino acid sequence of SEQ ID NO: 114; the CDR2 comprises the amino acid sequence of SEQ ID NO: 126; and the CDR3 comprises the amino acid sequence of SEQ ID NO: 124; and wherein the human PSMA is a 100 kD Type II membrane glycoprotein expressed in prostate tissue.

2. (canceled)

3. The trispecific protein of claim 1, wherein the first domain comprises the amino acid sequence of SEQ ID NO: 1.

4. The PSMA targeting trispecific protein of claim 1, wherein the first domain is humanized or human.

5. The PSMA targeting trispecific protein of claim 1, wherein the first domain has a K.sub.D binding of 150 nM or less to CD3 on CD3 expressing cells.

6-7. (canceled)

8. The PSMA targeting trispecific protein of claim 1, wherein the second domain comprises the amino acid sequence of SEQ ID NO: 94.

9. The PSMA targeting trispecific protein of claim 1, wherein the third domain comprises the amino acid sequence of SEQ ID No: 130 or 140.

10. The PSMA targeting trispecific protein of claim 1, wherein the domains are linked by linkers L1 and L2, and wherein linkers L1 and L2 are each independently selected from (GS)n (SEQ ID NO: 153), (GGS)n (SEQ ID NO: 154), (GGGS)n (SEQ ID NO: 155), (GGSG)n (SEQ ID NO: 156), (GGSGG)n (SEQ ID NO: 157), or (GGGGS)n (SEQ ID NO: 158), wherein n is 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10.

11. The PSMA targeting trispecific protein of claim 10, wherein linkers L1 and L2 are each independently (GGGGS).sub.4 (SEQ ID NO: 159) or (GGGGS).sub.3 (SEQ ID NO: 160).

12. The PSMA targeting trispecific protein of claim 10, wherein the domains are linked in the order H.sub.2N-(C)-L1-(B)-L2-(A)-COOH.

13. The PSMA targeting trispecific protein of claim 1, wherein the protein is less than about 80 kDa.

14. The PSMA targeting trispecific protein of claim 1, wherein the protein is about 50 to about 75 kDa.

15. The PSMA targeting trispecific protein of claim 1, wherein the protein is less than about 60 kDa.

16. The PSMA targeting trispecific protein of claim 1, wherein the protein has an elimination half-time of at least about 50 hours.

17. The PSMA targeting trispecific protein of claim 1, wherein the protein has an elimination half-time of at least about 100 hours.

18. The PSMA targeting trispecific protein of claim 1, wherein the protein has increased tissue penetration as compared to an IgG to the same PSMA.

19. The PSMA targeting trispecific protein of claim 1, wherein the protein comprises an amino acid sequence of SEQ ID NO: 147 or 152.

20. (canceled)

21. A pharmaceutical composition comprising (i) the PSMA targeting trispecific protein according to claim 1, and (ii) a pharmaceutically acceptable carrier.

22-28. (canceled)

29. A method of treating prostate cancer expressing a PSMA, the method comprising administration of an effective amount of the pharmaceutical composition of claim 21 to a subject having said prostate cancer, wherein said human PSMA is a 100 kD type II membrane glycoprotein expressed in prostate tissue.

30. (canceled)