Patent application title: NOVEL PEPTIDES THAT ENHANCE TIGHT JUNCTION PERMEABILITY
Inventors:
Amir Tamiz (Silver Spring, MD, US)
Min Li (Forest Park, IL, US)
Assignees:
Alba Therapeutics Corporation
IPC8 Class: AC07K706FI
USPC Class:
514 218
Class name: Designated organic active ingredient containing (doai) peptide (e.g., protein, etc.) containing doai 5 or 6 amino acid residues in the peptide chain
Publication date: 2014-06-19
Patent application number: 20140171377
Abstract:
The present invention provides novel peptides that facilitate the opening
of mammalian tight junctions, i.e. tight junction agonists. The present
invention also provides methods for the treatment of disease by
administering to a subject suffering from the disease a composition
comprising a peptide tight junction agonist of the invention in
combination with a therapeutically effective amount of an active agent.Claims:
1. A peptide tight junction agonist comprising the amino acid sequence of
SEQ ID NO:1, with at least one amino acid substitution, deletion, or
insertion, or at least one chemical modification, with respect to SEQ ID
NO: 1.
2.-4. (canceled)
5. The tight junction agonist of claim 1, wherein the position corresponding to position 2 of SEQ ID NO: 1 is AllylGly.
6.-9. (canceled)
10. The tight junction agonist of claim 1, wherein the tight junction agonist has a terminal basic group after the position corresponding to position 5 or 6 of SEQ ID NO: 1.
11. The tight junction agonist of claim 10, wherein the basic functional group is an amine.
12. The tight junction agonist of claim 1 comprising a substitution of at least one non-genetically encoded amino acid.
13.-14. (canceled)
15. The tight junction agonist of claim 1, wherein the agonist is from 3 to 10 amino acids in length.
16.-17. (canceled)
18. The peptide tight junction agonist of claim 1, wherein the peptide comprises an amino acid sequence selected from the group of SEQ ID NOs: 2-90.
19.-25. (canceled)
26. The peptide tight junction agonist of claim 1, wherein the peptide comprises an amino acid sequence selected from the group consisting of SEQ ID NOs: 73-90.
27. The peptide tight junction agonist of claim 26, wherein the peptide comprises an amino acid sequence selected from the group consisting of SEQ ID NOs:73, 74, 76, 85, and 88.
28. (canceled)
29. A composition comprising the peptide tight junction agonist of claim 1.
30.-34. (canceled)
35. A pharmaceutical composition comprising the peptide tight junction agonist of claim 1 and at least one pharmaceutically acceptable excipient.
36.-40. (canceled)
41. A method of treating a disease in a subject in need thereof, comprising: administering to the subject an effective dose of the peptide tight junction agonist of claim 1.
42. A method of treating a disease in a subject in need thereof, comprising: administering to the subject an effective dose of the composition of claim 29.
43. A method of treating a disease in a subject in need thereof, comprising: administering to the subject an effective dose of the pharmaceutical composition of claim 35.
44.-48. (canceled)
Description:
PRIORITY
[0001] This application claims priority to US Provisional Application No 60/952,144 filed Jul. 26, 2007, U.S. Provisional Application No. 60/953,398 filed Aug. 1, 2007, U.S. Provisional Application No. 60/953,403 filed Aug. 1, 2007, and U.S. Provisional Application No. 60/953,405 filed Aug. 1, 2007, each of which is hereby incorporated by reference in its entirety.
FIELD OF THE INVENTION
[0002] The present invention provides novel peptides that enhance tight junction permeability and their use as therapeutic agents, and their use in materials and methods to facilitate the delivery of therapeutic agents. In some embodiments, novel peptides that enhance tight junction permeability (i.e., peptide tight junction agonists) are used in compositions to facilitate the uptake of therapeutic agents across biological barriers comprising tight junctions. In some embodiments, such peptide tight junction agonists are used in compositions to modulate an immune response in a subject. In some embodiments, such peptide tight junction agonists are used in compositions to raise an immune response against an antigen.
BACKGROUND
[0003] The tight junctions (tj) or zonula occludens (ZO) are one of the hallmarks of absorptive and secretory epithelia (Madara, J. Clin. Invest., 83:1089-1094 (1989); and Madara, Textbook of Secretory Diarrhea Eds. Lebenthal et al, Chapter 11, pages 125-138 (1990)). Tight junctions act as a barrier between apical and basolateral compartments, selectively regulating the passive diffusion of ions and water-soluble solutes through the paracellular (between cells) pathway (Gumbiner, Am. J. Physiol., 253 (Cell Physiol. 22):C749-C758 (1987)). This barrier maintains any gradient generated by the activity of pathways associated with the transcellular route (Diamond, Physiologist, 20:10-18 (1977)).
[0004] Variations in transepithelial conductance can usually be attributed to changes in the permeability of the paracellular pathway, since the resistances of enterocyte plasma membranes are relatively high (Madara, supra). The ZO represents the major barrier in this paracellular pathway, and the electrical resistance of epithelial tissues seems to depend on the number of transmembrane protein strands, and their complexity in the ZO, as observed by freeze-fracture electron microscopy (Madara et al, J. Cell Biol., 101:2124-2133 (1985)).
[0005] Zonula occludens toxin (ZOT), which is produced by Vibrio cholerae, has been characterized by Fasano et al., (Proc. Natl. Acad. Sci., USA, 8:5242-5246 (1991)) and the sequence has been determined (GenBank accession no. A43864). ZOT is a tight junction agonist and increases the intestinal permeability of rabbit ileal mucosa by modulating the structure of intercellular tight junctions. U.S. Pat. Nos. 5,827,534, 5,665,389, 5,908,825 disclose the use of ZOT to facilitate the uptake of therapeutic agents. U.S. patent publication nos. US-2006-0276403-A1 and US 2006-0165722 A1, and application Ser. No. 11/673,192 disclose peptide tight junction agonists that can be used to facilitate the uptake of therapeutic agents.
Drug Delivery
[0006] The low bioavailability (BA) of efficacious pharmacotherapeutic drugs continues to be a major obstacle in drug development and in many instances may be the deciding factor on whether or not a potent agent is developed. Many therapeutic agents experience low BA after oral administration due to poor absorption or susceptibility to first pass metabolism. A means of enhancing the gastrointestinal absorption of such drugs would significantly extend their therapeutic usefulness while decreasing the dose required to produce efficacy.
[0007] Absorption enhancers, including surfactants, fatty acids, and chitosan derivatives, have been used to modify bioavailability by either disruption of the cell membrane or modulation of the tight junctions (TJ). In general, the optimal absorption enhancer should possess the following qualities: its effect should be reversible, it should provide a rapid permeation enhancing effect on the intestinal cellular membrane, it should be non-cytotoxic at the effective concentration level without deleterious and/or irreversible effects on the cellular membrane or cytoskeleton of the TJ. Zonula Occludens Toxin (Zot), a 44.8 kDa protein (399 amino acids; AA) located in the cell envelope of the bacterial strain Vibrio cholerae, is capable of reversibly opening the TJ between cells and increasing the paracellular transport of many drugs in a non-toxic manner. Intensive investigation of the biological activity of Zot as an absorption enhancer was triggered by reports of effective oral administration of insulin with Zot in diabetic rats. Recently, a smaller 12 kDa fragment (AA 265-399) of Zot, referred to as delta G (ΔG), was introduced as the biologically active fragment of Zot. Amino acid comparison between Zot active fragment and Zonulin, combined with site-directed mutagenesis experiments, confirmed the presence of an octapeptide receptor-binding domain toward the amino terminus of the processed Zot.
[0008] Applicants disclose novel peptides that enhance tight junction permeability, and methods of increasing bioavailability of pharmacotherapeutic drugs. The novel peptides facilitate transport of pharmacotherapeutic drugs across biological barriers whose permeability is regulated by tight junctions and thereby allows for increased bioavailability of such drugs. The novel peptides of the present invention are advantageous in that they are non-toxic, their effects are reversible, they are devoid of endotoxin contamination, readily synthesized and inexpensive to produce and purify.
Vaccines
[0009] Vaccines have proven to be successful, highly acceptable methods for the prevention of infectious diseases. They are cost effective, and do not induce antibiotic resistance to the target pathogen or affect normal flora present in the host. In many cases, such as when inducing anti-viral immunity, vaccines can prevent a disease for which there are no viable curative or ameliorative treatments available.
[0010] As is well known in the art, vaccines function by triggering the immune system to mount a response to an immunogenic agent, or antigen (antigenic agent), typically an infectious organism or a portion thereof that is introduced into the body in a non-infectious or non-pathogenic form. Once the immune system has been "primed" or sensitized to the organism, later exposure of the immune system to this organism as an infectious pathogen results in a rapid and robust immune response that destroys the pathogen before it can multiply and infect enough cells in the host organism to cause disease symptoms. The agent or antigen used to induce the immune system can be the entire organism in a less infectious state, known as an attenuated organism, or in some cases, components of the organism such as carbohydrates, proteins or peptides representing various structural components of the organism.
[0011] In many cases, it is necessary to enhance the immune response to the antigens present in a vaccine in order to stimulate the immune system to a sufficient extent to make a vaccine effective, i.e., to confer immunity. Many protein and most peptide and carbohydrate antigens, administered alone, do not elicit a sufficient antibody response to confer immunity. Such antigens need to be presented to the immune system in such a way that they will be recognized as foreign and will elicit an immune response. To this end, adjuvants have been devised which stimulate the immune response.
[0012] The best known adjuvant, Freund's complete adjuvant, consists of a mixture of mycobacteria in an oil/water emulsion. Freund's adjuvant works in two ways: first, by enhancing cell and humoral-mediated immunity, and second, by blocking rapid dispersal of the antigen challenge (the "depot effect"). However, due to frequent toxic physiological and immunological reactions to this material, Freund's adjuvant cannot be used in humans. Another molecule that has been shown to have immunostimulatory or adjuvant activity is endotoxin, also known as lipopolysaccharide (LPS). LPS stimulates the immune system by triggering an "innate" immune response--a response that has evolved to enable an organism to recognize endotoxin (and the invading bacteria of which it is a component) without the need for the organism to have been previously exposed. While LPS is too toxic to be a viable adjuvant, molecules that are structurally related to endotoxin, such as monophosphoryl lipid A ("MPL") are being tested as adjuvants in clinical trials. Currently, however, the only FDA-approved adjuvant for use in humans is aluminum salts (Alum) which are used to "depot" antigens by precipitation of the antigens. Alum also stimulates the immune response to antigens.
[0013] Thus, there is a recognized need in the art for compounds which can be co-administered with antigens in order to stimulate the immune system to generate a more robust antibody response to the antigen than would be seen if the antigen were injected alone or with Alum. Further, because development of mucosal vaccines requires the use of specific adjuvants, adjuvants that work for systemic immunization such as Alum are generally not effective for mucosal immunization. Despite intensive research on adjuvants for mucosal vaccines in the last decade, no adjuvants have been registered for human use so far. The main issues in adjuvant research are efficacy and toxicity, and candidate mucosal adjuvants do not completely satisfy the criteria of high efficacy and absence of toxicity. Furthermore, most of the proposed mucosal adjuvants are complex molecules whose mechanism of action is poorly understood. Applicants provide herein non-toxic alternative peptide tight junction agonist adjuvants for inducing immune responses to an antigen.
[0014] Zonula Occludens Toxin (ZOT) from Vibrio cholerae was identified as an adjuvant for mucosal vaccination (Infect. Immun. 1999, 67:1287; Infect. Immun. 2003, 71:1897). Intranasal administration of ZOT with a soluble antigen in mice stimulated systemic humoral and cell-mediated responses as well as mucosal responses specific for the antigen Ovalbumin (Infect. Immun. 2003, 71:1897). ZOT is a protein of 44.8 kDa that binds a receptor on epithelial cells and modulates tight junctions, inducing the increase of mucosal barrier permeability. The effect of ZOT on tight junctions is reversible and does not cause tissue damage (J. Clin. Invest. 1995, 96:710). The receptor for ZOT on epithelial cells has been partially characterized and recently a mammalian protein with homology to ZOT has been identified and named Zonulin. Interestingly, this protein has been shown to be an endogenous regulator of tight junctions that is released by epithelial cells and binds to the same receptor used by ZOT (Ann. NY. Acad Sci. 2000, 915:214). The mechanism of ZOT as an adjuvant may involve binding to its receptor on the nasal mucosa, modulation of tight junctions and antigen passage in the submucosa, with subsequent exposure to cells of the immune system.
[0015] The development of mucosal vaccines for the prevention of infectious diseases is highly desirable. Mucosal vaccination has several advantages over parenteral vaccination. Mucosal immunization induces an immune response at the site of infection (locally). Furthermore, because of the intrinsic properties of the mucosal immune system, the immunization at one mucosal site can induce specific responses at distant sites (regionally). Such flexibility is important to address cultural and religious barriers to vaccination because protective immunity (for instance against sexually-transmitted diseases) may then be induced in segregated mucosal sites in a practical way. In addition to local responses against mucosally-acquired pathogens, mucosal vaccines induce systemic immunity, including humoral and cell-mediated responses. Thus, mucosal vaccination could be exploited for combating infections acquired through other routes (i.e., blood or skin). Finally, the administration of mucosal vaccines does not require the use of needles, which could increase vaccine compliance and negate concerns with blood transmissible infections. For all the above reasons mucosal vaccines may be used also to combat cancer, either with preventive or therapeutic vaccination. These vaccines may be both against cancers caused by infectious agents (such as Helicobacter pylori, Papilloma Virus, Herpes Virus) and cancers of different etiology (such as melanoma, colon cancer and others).
[0016] Interestingly, most human pathogens are acquired through the mucosal route, however, few mucosal vaccines are presently used. Of those currently used, the vaccine is based on a living attenuated microorganism. Further, purified antigens are not able to stimulate/induce an immune response per se when delivered at mucosal surfaces. Therefore, such vaccines require the use of specific adjuvants. Unfortunately, development of mucosal vaccines has been so far hampered by the lack of safe and effective adjuvants as described above. An effective mucosal adjuvant allows antigen (Ag) passage through a mucosal barrier and facilitates the induction of an Ag-specific immune response.
[0017] Applicants disclose novel peptides that enhance tight junction permeability, and methods of mucosal delivery of an antigen together with such peptides to induce systemic and/or mucosal responses specific for the antigen. The novel peptides facilitate delivery of the antigen through the mucosa and induce systemic and mucosal responses to the antigen. The novel peptides of the present invention are advantageous in that they are non-toxic, their effects are reversible, they are devoid of endotoxin contamination, readily synthesized and inexpensive to produce and purify.
[0018] There remains a need in the art for materials and methods to modulate immune responses and to facilitate the delivery of therapeutic agents. This need and others are met by the present invention.
SUMMARY OF THE INVENTION
[0019] The present invention provides novel peptide tight junction agonists (inducers). Generally, the peptide tight junction agonists comprise the amino acid sequence of SEQ ID NO:1, with at least one amino acid deletion, insertion, or substitution, or at least one chemical modification, with respect to SEQ ID NO: 1. For example, the peptide tight junction agonist may have from one to five amino acid substitutions with respect to SEQ ID NO: 1, while maintaining the activity as an agonist (inducer) of tight junction permeability. In certain embodiments, the tight junction agonist has an AllylGly at the position corresponding to position 2 of SEQ ID NO: 1.
[0020] Such peptide tight junction agonists of the invention may vary in length. In some embodiments, peptide tight junction agonists according to the invention may be from about three to about ten amino acids in length. In some embodiments, peptide tight junction agonists of the invention may comprise, consist essentially of, or consist of a peptide that comprises, consists essentially of, or consists of an amino acid sequence selected from the group consisting of SEQ ID NOs: 2-90. In some embodiments, peptide tight junction agonists of the invention may comprise, consist essentially of, or consist of a peptide that comprises, consists essentially of, or consists of the amino acid sequence of SEQ ID NO:2. In other embodiments, peptide tight junction agonists of the invention may comprise, consist essentially of, or consist of a peptide that comprises, consists essentially of, or consists of an amino acid sequence selected from the group consisting of SEQ ID NOs:5-21. In other embodiments, peptide tight junction agonists of the invention may comprise, consist essentially of, or consist of a peptide that comprises, consists essentially of, or consists of an amino acid sequence selected from the group consisting of SEQ ID NOs:22-38. In other embodiments, peptide tight junction agonists of the invention may comprise, consist essentially of, or consist of a peptide that comprises, consists essentially of, or consists of an amino acid sequence selected from the group consisting of SEQ ID NOs:39-54. In other embodiments, peptide tight junction agonists of the invention may comprise, consist essentially of, or consist of a peptide that comprises, consists essentially of, or consists of an amino acid sequence selected from the group consisting of SEQ ID NOs:55-72. In other embodiments, peptide tight junction agonists of the invention may comprise, consist essentially of, or consist of a peptide that comprises, consists essentially of, or consists of an amino acid sequence selected from the group consisting of SEQ ID NOs:73-90. In some embodiments, peptide tight junction agonists of the invention may comprise, consist essentially of, or consist of a peptide that comprises, consists essentially of, or consists of an amino acid sequence selected from the group consisting of SEQ ID NOs:15, 23, 25, 26, 27, 29, 30 and 42. Additional tight junction agonists of the invention are as shown in the sequence listing filed concurrently herewith.
[0021] The present invention also provides compositions, e.g., pharmaceutical compositions, comprising one or more peptide tight junction agonists of the invention. Suitable peptide tight junction agonists for use in the compositions of the invention include, but are not limited to, peptide tight junction agonists that comprise, consist essentially of, or consist of a peptide that comprises, consists essentially of, or consists of an amino acid sequence selected from the group consisting of SEQ ID NOs:2-90. In some embodiments, peptide tight junction agonists for use in the compositions of the invention may comprise, consist essentially of, or consist of a peptide that comprises, consists essentially of, or consists of the amino acid sequence of SEQ ID NO:2. In other embodiments, peptide tight junction agonists for use in the compositions of the invention may comprise, consist essentially of, or consist of a peptide that comprises, consists essentially of, or consists of an amino acid sequence selected from the group consisting of SEQ ID NOs:5-21. In other embodiments, peptide tight junction agonists for use in the compositions of the invention may comprise, consist essentially of, or consist of a peptide that comprises, consists essentially of, or consists of an amino acid sequence selected from the group consisting of SEQ ID NOs:22-38. In other embodiments, peptide tight junction agonists for use in the compositions of the invention may comprise, consist essentially of, or consist of a peptide that comprises, consists essentially of, or consists an amino acid sequence selected from the group consisting of SEQ ID NOs:39-54. In other embodiments, peptide tight junction agonists for use in the compositions of the invention may comprise, consist essentially of, or consist of a peptide that comprises, consists essentially of, or consists of an amino acid sequence selected from the group consisting of SEQ ID NOs:55-72. In other embodiments, peptide tight junction agonists for use in the compositions of the invention may comprise, consist essentially of, or consist of a peptide that comprises, consists essentially of, or consists of an amino acid sequence selected from the group consisting of SEQ ID NOs:73-90. In some embodiments, peptide tight junction agonists for use in the compositions of the invention include, but are not limited to, peptide tight junction agonists that comprise, consist essentially of, or consist of a peptide that comprises, consists essentially of, or consists of an amino acid sequence selected from the group consisting of SEQ ID NOs:15, 23, 25, 26, 27, 29, 30 and 42. Compositions of the invention may further comprise one or more additional active agents. Typically additional active agents may be therapeutic agents, imaging agents, and/or immunogenic agents. Examples of suitable additional therapeutic agents include, but are not limited to, glucose metabolism agents (e.g., insulin), antibiotics, antineoplastics, antihypertensives, antiepileptics, central nervous system agents, and immune system suppressants. Examples of suitable additional immunogenic agents include, but are not limited to, antigens. Suitable additional imaging agents include, but are not limited to, agents comprising one or more radioactive atoms. A pharmaceutical composition of the invention may comprise one or more pharmaceutically acceptable excipients.
[0022] Compositions of the invention, for example, pharmaceutical compositions, may be formulated for any type of delivery. For example, compositions of the invention may be formulated for intestinal delivery, e.g., may be delayed release compositions. Compositions of the invention may also be formulated for pulmonary delivery, oral delivery and/or transcutaneous delivery.
[0023] In one embodiment, the present invention provides a method of treating a disease in a subject in need thereof. Methods of the invention may comprise administering to the subject a pharmaceutical composition comprising one or more peptide tight junction agonists and one or more additional therapeutic agents. In one embodiment, the present invention provides a method of treating diabetes in a subject in need thereof. In another embodiment, the present invention provides a method of treating an excessive or undesirable immune response in a subject in need thereof. In another embodiment, the present invention provides a method of treating inflammation in a subject in need thereof. In specific embodiments, the present invention provides methods of treating inflammatory bowel disease in a subject in need thereof. Inflammatory bowel disease that can be treated using methods of the present invention may be Crohn's disease or ulcerative colitis. In another embodiment, the present invention provides methods of treating cancer in a subject in need thereof.
[0024] In certain embodiments, pharmaceutical compositions of the present invention may comprise one or more insulins and/or derivatives thereof. In other embodiments, pharmaceutical compositions of the present invention may comprise one or more anti-inflammatory agents. In other embodiments, pharmaceutical compositions of the present invention may comprise one or more immune-suppressive drugs, for example, cyclosporin A. In another embodiment, pharmaceutical compositions of the present invention may comprise one or more anticancer agents.
BRIEF DESCRIPTION OF THE DRAWINGS
[0025] FIG. 1 is a schematic showing the steps involved in solid phase synthesis of an exemplary tight junction agonist of the invention.
[0026] FIG. 2 is a bar graph showing the results of a Real-Time Cell Electronic Sensing assay comparing the activity of various compounds of the invention to known tight junction agonist peptide FCIGRL (SEQ ID NO: 1).
[0027] FIG. 3 is a fluorescence microscopy analysis of the effects of tight junction agonist FCIGRL (SEQ ID NO:1) on IEC6 cells grown in monolayer and stained for F-actin.
[0028] FIG. 4 is a fluorescence microscopy analysis of the effects of PT-gliadin, tight junction agonist FCIGRL (SEQ ID NO:1), and various doses of tight junction agonist FCIGR on IEC6 cells grown in monolayer and stained for F-actin.
[0029] FIG. 5 is a fluorescence microscopy analysis of the effects of tight junction agonist FCIGRL (SEQ ID NO:1) on CaCo-2 cells grown in monolayer and stained for tight junction protein ZO-1. Cells were grown 21 days in a 6 well filter and treated with the junction agonist (apical and basolateral) for 3 hours.
[0030] FIG. 6 is a fluorescence microscopy analysis of the effects of tight junction agonist FCIGR on CaCo-2 cells grown in monolayer and stained for tight junction protein ZO-1.
[0031] FIG. 7 is a dose response curve for the tight junction agonist of SEQ ID NO:2 in a Lucifer Yellow (LY) permeability assay as described in Example 1.
[0032] FIG. 8 is a fluorescence microscopy analysis comparing the effects of tight junction agonist FCIGRL (SEQ ID NO:1) and F-(Allyl)GIGRL (SEQ ID NO:2) on CaCo-2 cells grown in monolayer and stained for tight junction protein ZO-1. Cells were grown 21 days in a 6 well filter and treated with the junction agonist (apical and basolateral) for 3 hours.
[0033] FIG. 9 is a fluorescence microscopy analysis showing a dose response of F-(Allyl)GIGRL (SEQ ID NO:2) on redistribution of ZO-1 in CaCo-2 BBE (Brush Border Expressing) cells grown in monolayer.
[0034] FIG. 10 is a fluorescence microscopy analysis showing the effects of FCIGRL (SEQ ID NO:1) and F-(Allyl)GIGRL (SEQ ID NO:2) on actin rearrangement in HeLa cells after 15 minutes and 60 minutes.
[0035] FIG. 11 is a magnified version of the 60 minute panels of FIG. 10, showing actin cytoskeletal rearrangement to the borderline of cells with the tight junction agonists FCIGRL (SEQ ID NO:1) and F-(Allyl)GIGRL (SEQ ID NO:2).
DETAILED DESCRIPTION OF THE INVENTION
[0036] Tight Junction Agonists
[0037] As used herein, a "tight junction agonist" is a compound that mediates or induces or facilitates or augments the physiological, transient opening of tight junctions, for example, the tight junctions between adjacent epithelial cells. An example of a tight junction agonist is zonula occludens toxin (ZOT), which is produced by Vibrio cholerae. A ZOT receptor agonist is a compound which is believed to mediate tight junction opening through the same receptor utilized by ZOT. In some embodiments, a tight junction agonist may comprise a peptide.
[0038] As used herein a subject is any animal, e.g., mammal, upon which methods of the invention may be practiced and/or to which materials of the present invention may be administered. Subjects include, but are not limited to, humans.
[0039] Tight junction agonists of the invention may comprise peptide tight junction agonists. An exemplary peptide tight junction agonist is a peptide that comprises the amino acid sequence Phe Cys Ile Gly Arg Leu (SEQ ID NO:1). Additional examples of peptide tight junction agonists of the invention include, but are not limited to, peptides wherein one or more amino acids of SEQ ID NO:1 have been substituted with a different amino acid.
[0040] In certain embodiments, position 2 of SEQ ID NO:1 will be substituted. In preferred embodiments the Cysteine (Cys or C) residue at position 2 of SEQ ID NO:1 is replaced by an AllylGly residue. In such preferred embodiments the peptide tight junction agonist of the invention comprises the amino acids sequence Phe-AllylGly-Ile-Gly-Arg-Leu of SEQ ID NO:2. In some embodiments, more than one position of SEQ ID NO:2 will be substituted. Substitutions may be made at any of position(s) 1, 3, 4, 5 or 6 of SEQ ID NO:2. In some embodiments, substitutions are made at position 1 of SEQ ID NO:2. In some embodiments, substitutions are made at position 3 of SEQ ID NO:2. In some embodiments, substitutions are made at position 4 of SEQ ID NO:2. In some embodiments, substitutions are made at position 5 of SEQ ID NO:2. In some embodiments, substitutions are made at position 6 of SEQ ID NO:2. In some embodiments, additional substitutions may be made at positions 1, 3, 4, 5 and 6 of SEQ ID NO:2 In some embodiments, position 1 of SEQ ID NO:2 will be substituted with another naturally occurring amino acid. In some embodiments, position 1 of SEQ ID NO:2 will be substituted with a non-naturally occurring amino acid. In some embodiments, position 3 of SEQ ID NO:2 will be substituted with another naturally occurring amino acid. In some embodiments, position 3 of SEQ ID NO:2 will be substituted with a non-naturally occurring amino acid. In some embodiments, position 4 of SEQ ID NO:2 will be substituted with another naturally occurring amino acid. In some embodiments, position 4 of SEQ ID NO:2 will be substituted with a non-naturally occurring amino acid (e.g., non-genetically encoded). In some embodiments, position 5 of SEQ ID NO:2 will be substituted with another naturally occurring amino acid. In some embodiments, position 5 of SEQ ID NO:2 will be substituted with a non-naturally occurring amino acid. In some embodiments, position 6 of SEQ ID NO:2 will be substituted with another naturally occurring amino acid. In some embodiments, position 6 of SEQ ID NO:2 will be substituted with a non-naturally occurring amino acid. Non-naturally occurring amino acids of the present invention are listed in Table 7. In some embodiments, a peptide tight junction agonist may comprise one or more D-amino acids.
[0041] When the tight junction agonist is a peptide, any length of peptide may be used. Generally, the size of the peptide tight junction agonist will range from about 3 to about 100, from about 3 to about 90, from about 3 to about 80, from about 3 to about 70, from about 3 to about 60, from about 3 to about 50, from about 3 to about 40, from about 3 to about 30, from about 3 to about 25, from about 3 to about 20, from about 3 to about 15, from about 3 to about 10, from about 3 to about 9, from about 3 to about 8, from about 3 to about 7, from about 3 to about 6, from about 3 to about 5, or from about 3 to about 4 amino acids in length. As used herein, "about" used to modify a numerical value means within about 10% of the value. Peptide tight junction agonists of the invention may be about 3, 4, 5, 6, 7, 8, 9, 10 or more amino acids in length.
[0042] The peptide tight junction agonists can be chemically synthesized and purified using well-known techniques, such as described in High Performance Liquid Chromatography of Peptides and Proteins: Separation Analysis and Conformation, Eds. Mant et al., C.R.C. Press (1991), and a peptide synthesizer, such as Symphony (Protein Technologies, Inc); or by using recombinant DNA techniques, i.e., where the nucleotide sequence encoding the peptide is inserted in an appropriate expression vector, e.g., an E. coli or yeast expression vector, expressed in the respective host cell, and purified therefrom using well-known techniques. A schematic representation of a solid phase synthesis of an exemplary tight junction agonist of the invention is shown in FIG. 1.
[0043] As used herein, the term "peptide" includes molecules with conventional peptide backbones as well as peptidomimetics having modified backbones. Such modifications include, but are not limited to, cyclization, N-terminus modification and C-terminus modification (including addition or modification with a basic group such as an amine), peptide bond modification, including, but not limited to backbones containing CH2--NH, CH2--S, CH2--S--O, O═C--NH, CH2--O, CH2--CH2, S═C--NH, CH═CH or CF═CH. Methods for preparing peptidomimetic compounds are well known in the art and are specified in Quantitative Drug Design, C. A. Ramsden Gd., Chapter 17.2, F. Choplin Pergamon Press (1992), which is hereby incorporated by reference.
[0044] Compositions
[0045] Typically, compositions, such as pharmaceutical compositions, comprise a peptide tight junction agonist and optionally one or more additional active agents. Peptide tight junction agonists may be present in an amount sufficient to facilitate the opening of tight junctions, for example, the tight junctions between adjacent epithelial cells; or in amount sufficient to modulate an immune response to an antigen; or in an amount sufficient to reduce inflammation, in a subject in need thereof. The amount of agonist (e.g., peptide tight junction agonist) employed in any given composition may vary according to factors such as the disease state, age, sex, and weight of the subject. Dosage regimens may be adjusted to provide the optimum therapeutic response. For example, a single bolus may be administered, several divided doses may be administered over time or the dose may be proportionally reduced or increased as indicated by the exigencies of the therapeutic situation.
[0046] Generally, a pharmaceutical composition of the invention will comprise an amount of peptide tight junction agonist in the range of about 1 μg to about 1 g, preferably about 1 mg to about 1000 mg, from about 10 mg to about 100 mg, from about 10 mg to about 50 mg, or from about 10 mg to about 25 mg of peptide tight junction agonist. As used herein, "about" used to modify a numerical value means within 10% of the value.
[0047] Compositions of the invention may comprise one or more peptide tight junction agonists at a level of from about 0.1 wt % to about 20 wt %, from about 0.1 wt % to about 18 wt %, from about 0.1 wt % to about 16 wt %, from about 0.1 wt % to about 14 wt %, from about 0.1 wt % to about 12 wt %, from about 0.1 wt % to about 10 wt %, from about 0.1 wt % to about 8 wt %, from about 0.1 wt % to about 6 wt %, from about 0.1 wt % to about 4 wt %, from about 0.1 wt % to about 2 wt %, from about 0.1 wt % to about 1 wt %, from about 0.1 wt % to about 0.9 wt %, from about 0.1 wt % to about 0.8 wt %, from about 0.1 wt % to about 0.7 wt %, from about 0.1 wt % to about 0.6 wt %, from about 0.1 wt % to about 0.5 wt %, from about 0.1 wt % to about 0.4 wt %, from about 0.1 wt % to about 0.3 wt %, or from about 0.1 wt % to about 0.2 wt % of the total weight of the composition. As used herein, "about" used to modify a numerical value means within 10% of the value. Compositions of the invention may comprise one or more peptide tight junction agonists at a level of about 0.1 wt %, about 0.2 wt %, about 0.3 wt %, about 0.4 wt %, about 0.5 wt %, about 0.6 wt %, about 0.7 wt %, about 0.8 wt %, or about 0.9 wt % based on the total weight of the composition.
[0048] Compositions of the invention may comprise one or more peptide tight junction agonists at a level of from about 1 wt % to about 20 wt %, from about 1 wt % to about 18 wt %, from about 1 wt % to about 16 wt %, from about 1 wt % to about 14 wt %, from about 1 wt % to about 12 wt %, from about 1 wt % to about 10 wt %, from about 1 wt % to about 9 wt %, from about 1 wt % to about 8 wt %, from about 1 wt % to about 7 wt %, from about 1 wt % to about 6 wt %, from about 1 wt % to about 5 wt %, from about 1 wt % to about 4 wt %, from about 1 wt % to about 3 wt %, or from about 1 wt % to about 2 wt % of the total weight of the composition. As used herein, "about" used to modify a numerical value means within 10% of the value. Compositions of the invention may comprise one or more peptide tight junction agonists at a level of about 1 wt %, about 2 wt %, about 3 wt %, about 4 wt %, about 5 wt %, about 6 wt %, about 7 wt %, about 8 wt %, or about 9 wt % based on the total weight of the composition.
[0049] Compositions of the invention, for example, pharmaceutical compositions comprising one or more peptide tight junction agonists and one or more additional active agents, may be formulated for pulmonary delivery (e.g., may be pulmonary dosage forms). Typically such compositions may be provided as pharmaceutical aerosols, e.g., solution aerosols or powder aerosols. Those of skill in the art are aware of many different methods and devices for the formation of pharmaceutical aerosols, for example, those disclosed by Sciarra and Sciarra, Aerosols, in Remington: The Science and Practice of Pharmacy, 20th Ed., Chapter 50, Gennaro et al. Eds., Lippincott, Williams and Wilkins Publishing Co., (2000).
[0050] In one embodiment, the dosage forms are in the form of a powder aerosol (i.e, comprise particles). These are particularly suitable for use in inhalation delivery systems. Powders may comprise particles of any size suitable for administration to the lung.
[0051] Powder formulations may optionally contain at least one particulate pharmaceutically acceptable carrier known to those of skill in the art. Examples of suitable pharmaceutical carriers include, but are not limited to, saccharides, including monosaccharides, disaccharides, polysaccharides and sugar alcohols such as arabinose, glucose, fructose, ribose, mannose, sucrose, trehalose, lactose, maltose, starches, dextran, mannitol or sorbitol. In one embodiment, a powder formulation may comprise lactose as a carrier.
[0052] Powder formulations may be contained in any container known to those in the art. Containers may be capsules of, for example, gelatin or plastic, or in blisters (e.g. of aluminum or plastic), for use in a dry powder inhalation device. In some embodiments, the total weight of the formulation in the container may be from about 5 mg to about 50 mg. In other embodiments, powder formulations may be contained in a reservoir in a multi-dose dry powder inhalation device adapted to deliver a suitable amount per actuation.
[0053] Powder formulations typically comprise small particles. Suitable particles can be prepared using any means known in the art, for example, by grinding in an airjet mill, ball mill or vibrator mill, sieving, microprecipitation, spray-drying, lyophilisation or controlled crystallisation. Typically, particles will be about 10 microns or less in diameter. Particles for use in the compositions of the invention may have a diameter of from about 0.1 microns to about 10 microns, from about 0.1 microns to about 9 microns, from about 0.1 microns to about 8 microns, from about 0.1 microns to about 7 microns, from about 0.1 microns to about 6 microns, from about 0.1 microns to about 5 microns, from about 0.1 microns to about 4 microns, from about 0.1 microns to about 3 microns, from about 0.1 microns to about 2 microns, from about 0.1 microns to about 1 micron, from about 0.1 microns to about 0.5 microns, from about 1 micron to about 10 microns, from about 1 micron to about 9 microns, from about 1 micron to about 8 microns, from about 1 micron to about 7 microns, from about 1 micron to about 6 microns, from about 1 micron to about 5 microns, from about 1 micron to about 4 microns, from about 1 micron to about 3 microns, from about 1 micron to about 2 microns, from about 2 microns to about 10 microns, from about 2 microns to about 9 microns, from about 2 microns to about 8 microns, from about 2 microns to about 7 microns, from about 2 microns to about 6 microns, from about 2 microns to about 5 microns, from about 2 microns to about 4 microns, or from about 2 microns to about 3 microns. As used herein, "about" used to modify a numerical value means within 10% of the value. In some embodiments, particles for use in the invention may be about 1 micron, about 2 microns, about 3 microns, about 4 microns, about 5 microns, about 6 microns, about 7 microns, about 8 microns, about 9 microns, or about 10 microns in diameter.
[0054] In one embodiment, the dosage forms are in the form of a solution aerosol (i.e., comprise droplets). Typically, droplets will be about 10 microns or less in diameter. Droplets for use in the compositions of the invention may have a diameter of from about 0.1 microns to about 10 microns, from about 0.1 microns to about 9 microns, from about 0.1 microns to about 8 microns, from about 0.1 microns to about 7 microns, from about 0.1 microns to about 6 microns, from about 0.1 microns to about 5 microns, from about 0.1 microns to about 4 microns, from about 0.1 microns to about 3 microns, from about 0.1 microns to about 2 microns, from about 0.1 microns to about 1 micron, from about 0.1 microns to about 0.5 microns, from about 1 micron to about 10 microns, from about 1 micron to about 9 microns, from about 1 micron to about 8 microns, from about 1 micron to about 7 microns, from about 1 micron to about 6 microns, from about 1 micron to about 5 microns, from about 1 micron to about 4 microns, from about 1 micron to about 3 microns, from about 1 micron to about 2 microns, from about 2 microns to about 10 microns, from about 2 microns to about 9 microns, from about 2 microns to about 8 microns, from about 2 microns to about 7 microns, from about 2 microns to about 6 microns, from about 2 microns to about 5 microns, from about 2 microns to about 4 microns, or from about 2 microns to about 3 microns. As used herein, "about" used to modify a numerical value means within 10% of the value. In some embodiments, particles and/or droplets for use in the invention may be about 1 micron, about 2 microns, about 3 microns, about 4 microns, about 5 microns, about 6 microns, about 7 microns, about 8 microns, about 9 microns, or about 10 microns in diameter.
[0055] The compositions of the invention may be formulated for enteric delivery, for example, may comprise one or more coatings including, for example, a delayed release coating containing one or more enteric agents. A delayed release coating is typically substantially stable in gastric fluid and substantially unstable (e.g., dissolves rapidly or is physically unstable) in intestinal fluid, thus providing for substantial release of the peptide tight junction agonist and/or active agent from the composition in the duodenum or the jejunum.
[0056] The term "stable in gastric fluid" refers to a composition that releases 30% or less by weight of the total peptide tight junction agonist and/or active agent in the composition in gastric fluid with a pH of 5 or less, or simulated gastric fluid with a pH of 5 or less, in approximately sixty minutes. Examples of simulated gastric fluid and simulated intestinal fluid include, but are not limited to, those disclosed in the 2005 Pharmacopeia 23NF/28USP in Test Solutions at page 2858 and/or other simulated gastric fluids and simulated intestinal fluids known to those of skill in the art, for example, simulated gastric fluid and/or intestinal fluid prepared without enzymes.
[0057] Compositions of the of the invention may release from about 0% to about 30%, from about 0% to about 25%, from about 0% to about 20%, from about 0% to about 15%, from about 0% to about 10%, from about 5% to about 30%, from about 5% to about 25%, from about 5% to about 20%, from about 5% to about 15%, from about 5% to about 10% by weight of the total peptide tight junction agonist and/or active agent in the composition in gastric fluid with a pH of 5 or less, or simulated gastric fluid with a pH of 5 or less, in approximately sixty minutes. As used herein, "about" used to modify a numerical value means within 10% of the value. Compositions of the invention may release about 1%, about 2%, about 3%, about 4%, about 5%, about 6%, about 7%, about 8%, about 9%, or about 10% by weight of the total peptide tight junction agonist in the composition in gastric fluid with a pH of 5 or less, or simulated gastric fluid with a pH of 5 or less, in approximately sixty minutes.
[0058] The term "unstable in intestinal fluid" refers to a composition that releases 70% or more by weight of the total peptide tight junction agonist and/or active agent in the composition in intestinal fluid or simulated intestinal fluid in approximately sixty minutes. The term "unstable in near neutral to alkaline environments" refers to a composition that releases 70% or more by weight of the total amount of tight junction agonist and/or active agent in the composition in intestinal fluid with a pH of 5 or greater, or simulated intestinal fluid with a pH of 5 or greater, in approximately ninety minutes. For example, a composition that is unstable in near neutral or alkaline environments may release 70% or more by weight of a tight junction agonist and/or active agent in a fluid having a pH greater than about 5 (e.g., a fluid having a pH of from about 5 to about 14, from about 6 to about 14, from about 7 to about 14, from about 8 to about 14, from about 9 to about 14, from about 10 to about 14, or from about 11 to about 14) in from about 5 minutes to about 90 minutes, from about 10 minutes to about 90 minutes, from about 15 minutes to about 90 minutes, from about 20 minutes to about 90 minutes, from about 25 minutes to about 90 minutes, from about 30 minutes to about 90 minutes, from about 5 minutes to about 60 minutes, from about 10 minutes to about 60 minutes, from about 15 minutes to about 60 minutes, from about 20 minutes to about 60 minutes, from about 25 minutes to about 60 minutes, or from about 30 minutes to about 60 minutes. As used herein, "about" used to modify a numerical value means within 10% of the value.
[0059] Compositions of the invention may be formulated for transcutaneous delivery (e.g., may be transcutaneous dosage forms). Typically such compositions may be provided as topical solutions and/or gels. Those of skill in the art are aware of many different methods and devices for the formation of topical medications, for example, those disclosed by Block, Medicated Topicals, in Remington: The Science and Practice of Pharmacy, 20th Ed., Chapter 44, Gennaro et al. Eds., Lippincott, Williams and Wilkins Publishing Co., (2000).
[0060] Additional Active Agents
[0061] In addition to one or more peptide tight junction agonists, compositions of the invention may further comprise one or more additional active agents, e.g., therapeutic agents, immunogenic agents and/or imaging agents.
[0062] Additional therapeutic agents that can be used in the compositions of the invention include agents that act on any organ of the body, such as heart, brain, intestine, or kidneys. Suitable additional therapeutic agents include, but are not limited to, glucose metabolism agents (e.g., insulin), antibiotics, antineoplastics, antihypertensives, antiepileptics, central nervous system agents, anti-inflammatory agents and immune system suppressants.
[0063] Additional therapeutic agents that can be used in the compositions of the invention include immunosuppressive agents. Such immunosuppressants used in the method and composition of the invention can be any agent which tends to attenuate the activity of the humoral or cellular immune systems. In particular, in one aspect the invention comprises compositions wherein the immunosuppressant is selected from the group consisting of cyclosporin A, FK506, prednisone, methylprednisolone, cyclophosphamide, thalidomide, azathioprine, and daclizumab, physalin B, physalin F, physalin G, seco-steroids purified from Physalis angulata L., 15-deoxyspergualin (DSG, 15-dos), MMF, rapamycin and its derivatives, CCI-779, FR 900520, FR 900523, NK86-1086, depsidomycin, kanglemycin-C, spergualin, prodigiosin25-c, cammunomicin, demethomycin, tetranactin, tranilast, stevastelins, myriocin, gliooxin, FR 651814, SDZ214-104, bredinin, WS9482, mycophenolic acid, mimoribine, misoprostol, OKT3, anti-IL-2 receptor antibodies, azasporine, leflunomide, mizoribine, azaspirane (SKF 105685), paclitaxel, altretamine, busulfan, chlorambucil, ifosfamide, mechlorethamine, melphalan, thiotepa, cladribine, fluorouracil, floxuridine, gemcitabine, thioguanine, pentostatin, methotrexate, 6-mercaptopurine, cytarabine, carmustine, lomustine, streptozotocin, carboplatin, cisplatin, oxaliplatin, iproplatin, tetraplatin, lobaplatin, JM216, JM335, fludarabine, aminoglutethimide, flutamide, goserelin, leuprolide, megestrol acetate, cyproterone acetate, tamoxifen, anastrozole, bicalutamide, dexamethasone, diethylstilbestrol, bleomycin, dactinomycin, daunorubicin, doxirubicin, idarubicin, mitoxantrone, losoxantrone, mitomycin-c, plicamycin, paclitaxel, docetaxel, topotecan, irinotecan, 9-amino camptothecan, 9-nitro camptothecan, GS-211, etoposide, teniposide, vinblastine, vincristine, vinorelbine, procarbazine, asparaginase, pegaspargase, octreotide, estramustine, and hydroxyurea, and combinations thereof. In one more particular aspect, the immunosuppressant is cyclosporin A.
[0064] Furthermore, the additional therapeutic agent can be selected from the group consisting of a chemotherapeutic, a gene therapy vector, a growth factor, a contrast agent, an angiogenesis factor, a radionuclide, an anti-infection agent, an anti-tumor compound, a receptor-bound agent, a hormone, a steroid, a protein, a complexing agent, a polymer, a thrombin inhibitor, an antithrombogenic agent, a tissue plasminogen activator, a thrombolytic agent, a fibrinolytic agent, a vasospasm inhibitor, a calcium channel blocker, a nitrate, a nitric oxide promoter, a vasodilator, an antihypertensive agent, an antimicrobial agent, an antibiotic, a glycoprotein IIb/IIIa inhibitor, an inhibitor of surface glycoprotein receptors, an antiplatelet agent, an antimitotic, a microtubule inhibitor, a retinoid, an antisecretory agent, an actin inhibitor, a remodeling inhibitor, an antisense nucleotide, an agent for molecular genetic intervention, an antimetabolite, an antiproliferative agent, an anti-cancer agent, a dexamethasone derivative, an anti-inflammatory steroid, a non-steroidal anti-inflammatory agent, an immunosuppressive agent, a PDGF antagonist, a growth hormone antagonist, a growth factor antibody, an anti-growth factor antibody, a growth factor antagonist, a dopamine agonist, a radiotherapeutic agent, an iodine-containing compound, a barium-containing compound, a heavy metal functioning as a radiopaque agent, a peptide, a protein, an enzyme, an extracellular matrix component, a cellular component, an angiotensin converting enzyme inhibitor, a 21-aminosteroid, a free radical scavenger, an iron chelator, an antioxidant, a sex hormone, an antipolymerase, an antiviral agent, an IgG2 Kappa antibody against Pseudomonas aeruginosa exotoxin A and reactive with A431 epidermoid carcinoma cells, monoclonal antibody against the noradrenergic enzyme dopamine beta-hydroxylase conjugated to saporin or other antibody targeted therapy agents, gene therapy agents, a prodrug, a photodynamic therapy agent, and an agent for treating benign prostatic hyperplasia (BHP), a 14C--, 3H--, 131I--, 32P-- or 36S-radiolabelled form or other radiolabelled form of any of the foregoing, and combinations thereof.
[0065] More particularly, the additional therapeutic agent can be selected from the group consisting of parathyroid hormone, heparin, human growth hormone, covalent heparin, hirudin, hirulog, argatroban, D-phenylalanyl-L-poly-L-arginyl chloromethyl ketone, urokinase, streptokinase, nitric oxide, triclopidine, aspirin, colchicine, dimethyl sulfoxide, cytochalasin, deoxyribonucleic acid, methotrexate, tamoxifen citrate, dexamethasone, dexamethasone sodium phosphate, dexamethasone acetate, cyclosporin, trapidal, angiopeptin, angiogenin, dopamine, 60Co, 192Ir, 32P, 111In, 90Y, 99mTc, pergolide mesylate, bromocriptine mesylate, gold, tantalum, platinum, tungsten, captopril, enalapril, ascorbic acid, α-tocopherol, superoxide dismutase, deferoxamine, estrogen, azidothymidine (AZT), acyclovir, famciclovir, rimantadine hydrochloride, ganciclovir sodium, 5-aminolevulinic acid, meta-tetrahydroxyphenylchlorin, hexadecafluoro zinc phthalocyanine, tetramethyl hematoporphyrin, and rhodamine 123, and combinations thereof.
[0066] Compositions of the invention may comprise one or more immunogenic agents, for example, antigens. Examples of antigens that can be used in the compositions of the invention (e.g., immunogenic and/or vaccine compositions) include peptides, proteins, microorganisms (e.g., attenuated and/or recombinant microorganisms), cells (e.g., cancer cells and/or recombinant cells) and viruses (e.g., attenuated and/or recombinant viruses). Examples of peptide antigens include the B subunit of the heat-labile enterotoxin of enterotoxigenic E. coli, the B subunit of cholera toxin, capsular antigens of enteric pathogens, fimbriae or pili of enteric pathogens, HIV surface antigens, cancer antigens (e.g., cancer cells comprising antigens, isolated antigens, etc.), dust allergens, and acari allergens. Other immunogenic compounds as are known in the art can also be used.
[0067] Examples of attenuated microorganisms and viruses that can be used in the compositions of the invention (e.g., vaccine compositions) include those of enterotoxigenic Escherichia coli, enteropathogenic Escherichia coli, Vibrio cholerae, Shigella flexneri, Salmonella typhi and rotavirus (Fasano et al, In: Le Vaccinazioni in Pediatria, Eds. Vierucci et al, CSH, Milan, pages 109-121 (1991); Guandalini et al, In: Management of Digestive and Liver Disorders in Infants and Children, Elsevior, Eds. Butz et al, Amsterdam, Chapter 25 (1993); Levine et al, Sem. Ped. Infect. Dis., 5.243-250 (1994); and Kaper et al, Clin. Micrbiol. Rev., 8:48-86 (1995), each of which is incorporated by reference herein in its entirety).
[0068] Any antigen capable of inducing a protective immune response may be used in the vaccine compositions of the invention. Examples of suitable antigens include, but are not limited to, measles virus antigens, mumps virus antigens, rubella virus antigens, Corynebacterium diphtheriae antigens, Bordetella pertussis antigens, Clostridium tetani antigens, Bacillus anthracis antigens, Haemophilus influenzae antigens, smallpox virus antigens, and influenza virus antigens.
[0069] Compositions of the invention may further comprise one or more protease inhibitors. Any protease inhibitor can be used, including, but not limited to, a proteinase, peptidase, endopeptidase, or exopeptidase inhibitor. A cocktail of inhibitors can also be used. Alternatively, the protease inhibitors can be selected from the group consisting of bestatin, L-trans-3-carboxyoxiran-2-carbonyl-L-leucylagmatine, ethylenediaminetetraacetic acid (EDTA), phenylmethylsulfonylfluoride (PMSF), aprotinin, amyloid protein precursor (APP), amyloid beta precursor protein, α1-proteinase inhibitor, collagen VI, bovine pancreatic trypsin inhibitor (BPTI), 4-(2-aminoethyl)-benzenesulfonyl fluoride (AEBSF), antipain, benzamidine, chymostatin, ε-aminocaproate, N-ethylmaleimide, leupeptin, pepstatin A, phosphoramidon, and combinations thereof. Novel protease inhibitors can also be used. Indeed, protease inhibitors can be specifically designed or selected to decrease the proteolysis of the tight junction agonist and/or the therapeutic agent.
[0070] Compositions of the invention may also comprise one or more pharmaceutically acceptable excipients. Suitable excipients include, but are not limited to, buffers, buffer salts, bulking agents, salts, surface active agents, acids, bases, sugars, binders, and the like.
[0071] Methods of Treatment
[0072] Peptide tight junction agonists and pharmaceutical compositions of the invention can be used for treating, ameliorating, and/or preventing a disease. Any disease may be treated using the compositions of the invention by selection of an appropriate active agent, e.g., therapeutic and/or immunogenic agent. In one embodiment, the present invention provides a method of treating diabetes response in a subject (e.g., a mammal such as a human) by administering a composition comprising one or more peptide tight junction agonists together with one or more insulins and/or derivatives thereof. In another embodiment, the invention provides a method of suppressing an excessive or undesirable immune response in a subject (e.g., a mammal such as a human) by administering a composition comprising one or more peptide tight junction agonists together with one or more immune-suppressive drugs that may include, for example, cyclosporin A.
[0073] Examples of diseases that can be treated using the compositions of the invention include, but are not limited to, cancer, autoimmune diseases, vascular disease, bacterial infections, gastritis, gastric cancer, collagenous colitis, inflammatory bowel disease, osteoporosis, systemic lupus erythematosus, food allergy, asthma, and irritable bowel syndrome. For example, to treat inflammatory bowel disease, a composition comprising one or more peptide tight junction agonists may be administered to the subject (e.g., a mammal such as a human) in need thereof.
[0074] In another example, to treat cancer of the colon or rectal area, a composition comprising a therapeutically effective amount of Erbitux® (Cetuximab) together with an absorption enhancing amount of one or more peptide tight junction agonists may be administered to the subject (e.g., a mammal such as a human) in need thereof. In another example, to treat breast cancer, a composition comprising a therapeutically effective amount of Herceptin® (Trastuzumab) together with an absorption enhancing amount of one or more peptide tight junction agonists may be administered to the subject (e.g., a mammal such as a human) in need thereof. In another example, to treat various types of cancer, a composition comprising a therapeutically effective amount of Avastin® (Bevacizumab) together with an absorption enhancing amount of one or more peptide tight junction agonists may be administered to the subject (e.g., a mammal such as a human) in need thereof. Another example involves treatment of osteoporosis by administration of a composition comprising one or more peptide tight junction agonists together with a therapeutically effective amount of Fosamax® (Alendronate) to the subject in need thereof. Another example involves treatment of transplant rejection by administration of a composition comprising one or more peptide tight junction agonists together with a therapeutically effective amount of Cyclosporin A to the subject in need thereof. Another example involves treatment of anemia by administration of a composition comprising one or more peptide tight junction agonists together with a therapeutically effective amount of erythropoietin to the subject in need thereof. Another example involves treatment of hemophilia by administration of a composition comprising one or more peptide tight junction agonists together with a therapeutically effective amount of Factor VIII to the subject in need thereof.
[0075] In some embodiments, compositions of the invention (e.g., pharmaceutical compositions) may be given repeatedly over a protracted period, i.e., may be chronically administered. Typically, compositions may be administered one or more times each day in an amount suitable to prevent, reduce the likelihood of an attack of, or reduce the severity of an attack of the underlying disease condition (e.g., diabetes, cancer, transplant rejection, etc). Such compositions may be administered chronically, for example, one or more times daily over a plurality of days.
[0076] In some embodiments, compositions of the invention (e.g., pharmaceutical compositions) may be used to treat acute attacks of the underlying disease (e.g., diabetes, cancer, transplant rejection, etc). Typically, embodiments of this type will require administration of the compositions of the invention to a subject undergoing an attack in an amount suitable to reduce the severity of the attack. One or more administrations may be used.
[0077] In some embodiments, peptide tight junction agonists of the invention may be used in the manufacture of compositions and pharmaceutical compositions for use in the methods described above.
[0078] The following examples are provided for illustrative purposes only, and are in no way intended to limit the scope of the present invention.
EXAMPLES
Example 1
Measurement of Trans Epithelial Electric Resistance (TEER) and Epithelial Flux of a Fluorescent Marker Lucifer Yellow
[0079] CaCo2 cells form monolayers that exhibit tight junctions between adjacent cells. Agonists of tight junctions can be identified by their ability to enhance the flux of compounds (e.g. ions, Lucifer Yellow) through a cell monolayer that comprises tight junctions; or by their ability to reduce TEER across a cell monolayer that comprises tight junctions. Treatment of CaCo2 monolayers with peptide FCIGRL (SEQ ID NO: 1) led to a 51-fold enhancement of Lucifer Yellow permeability through CaCo2 monolayers compared to vehicle alone. Further, FIG. 7 shows a dose response curve for the tight junction agonist of SEQ ID NO:2 in the Lucifer Yellow (LY) permeability assay.
[0080] Treatment of CaCo2 monolayers with peptide FCIGRL led to a 16-fold decrease in TEER across CaCo2 monolayers compared to vehicle alone.
[0081] Tight Junction Agonists can be Identified and Tested Using the Following Method:
[0082] Determination of TEER and Lucifer Yellow Flux
[0083] Prepare Modified Hank's Balanced Salt Solution (MHBSS) by obtaining 1 L bottle of HBSS removing 10 ml of HBSS and replacing it with 10 ml HEPES buffer pH 7.0. Adjust pH to 7.4±0.1 using concentrated NaOH (10N).
[0084] Remove CaCo-2 cells from incubator, grown on 12-well, 3.0 μM, polycarbonate Transwell® filters (Corning) and record passage#, date cells seeded and age in days.
[0085] Aspirate cell culture medium from both the apical (AP) and basolateral (BL) compartments, replacing with 0.5 ml and 1.5 ml of MHBSS, respectively. Incubate cells at 37° C. for 30 minutes.
[0086] Using the MilliCell®-ERS instrument (Millipore), measure and record the transepithelial electrical resistance (TEER) across each filter and record.
[0087] Aspirate solution from the apical compartment of each filter (n=3 per condition) and replace with 0.5 ml of control and test solutions containing Lucifer Yellow and test compound if appropriate.
[0088] Place all plates into incubator set at 37° C. (±0.2), 50 RPM (±5) for a total of 180 minutes.
[0089] At t=30, 60, 120 and 180 minutes, measure and record the transepithelial electrical resistance (TEER) across each filter using the MilliCell-ERS instrument.
[0090] At t=60, 120 and 180 minutes remove 1000 from each basolateral compartment and place it in a 96-well plate for Lucifer Yellow analysis, replace with 100 μl of MHBSS.
[0091] Make a Lucifer Yellow standard curve with the following dilutions (7500 μM, 3750 μM, 750 μM, 375 μM, 75 μM, 37.5 μM, 7.5 μM, 3.75 μM, 0.75 μM) and pipette 100 μL of each into a 96-well plate except for the first three standards mentioned above which require a 1:10 dilutions prior to transferring to the 96-well plate.
[0092] Harvest the remaining start solutions and what is left in each apical compartment into 1.5 ml vials. Freeze at -20° C. for future analysis.
[0093] Analyze each 96-well plate in a Tecan Spectra Fluor Plus using Magellan at 485 and 535 nm.
[0094] Materials:
[0095] Cells: CaCo-2 cells passage 40-60 grown on Transwell® plates for 21-28 days
[0096] Culture Medium: DMEM supplemented with 10% fetal bovine serum, 1% NEAA, 1% Penn/Strep
[0097] Buffers: Hank's Balanced Salt Solution (HBSS) without calcium and magnesium
[0098] Flasks: 100×20 mm Tissue culture dish Falcon.
[0099] Plates: 12 well polycarbonate Transwell® filters; 0.3 uM pore size
Example 2
Identification of Tight Junction Agonists Using Real-Time Cell Electronic Sensing (RT-CES)
[0100] IEC6 cells form monolayers that exhibit tight junctions between adjacent cells. Agonists of tight junctions can be identified by their ability to induce changes in morphology of cells in a monolayer of cells that comprise tight junctions. Such changes in the morphology of IEC6 cells may be measured using a Real-Time Cell Electronic Sensing protocol as described below.
[0101] Tight junction agonists can be identified using the following method:
[0102] Materials: cells: IEC6 passage 30-50, medium: DMEM 10% no calcium no magnesium, foetal bovine serum 0.1 unit per ml bovine insulin, buffers: phosphate buffered saline (PBS) no calcium no magnesium, trypsin: 0.25% porcine trypsin in HBSS no calcium no magnesium, flasks: 100×20 mm Tissue culture dish Falcon, plates: 16× E-Plate, machine: RT-CEST® 16× system (ACEA Biosciences, Inc., San Diego, Calif.)
[0103] Wash a 75 cm2 flask of confluent IEC6 cells twice with 25 ml of PBS.
[0104] Add 2.5 ml of trypsin to the flask and place back in the incubator at 37° C.
[0105] Wash cells from the surface of the flask with 10 ml of serum containing media to quench the trypsin.
[0106] Pellet the cells by centrifugation at 1500 rpm for 5 minutes aspirate the media.
[0107] Resuspend the cell pellet in 10 ml of serum free media and centrifuge at 1500 rpm for 5 minutes aspirate the media and repeat for a total of 5 washes.
[0108] Take 100 μl of cells and mix with 100 μl of trypan blue.
[0109] Count the cells four times and use the average cell concentration.
[0110] Dilute the cells to 1×106 per ml in serum free media.
[0111] Add 100 μl of serum free media to each well of the ACEA plates to be used.
[0112] Insert the ACEA plate and press scan.
[0113] Run step 1 of the program to measure background.
[0114] Add 50 μl of cells to each well of the ACEA plate tap each slide of the plate 10 times and place the cells on the bench for 15 minutes to allow the cells to settle.
[0115] Insert the ACEA plate and run the scan step to check connections and run step 2-1 and 2-2 overnight.
[0116] Step 2-1 sample every 2 minutes 30 times.
[0117] Step 2-2 sample every 15 minutes 100 times.
[0118] The cell indices should be between 6-10 after the overnight run and should have reached a plateau.
[0119] Remove 100 μl of media carefully from each well.
[0120] Make up the compounds to be tested so that 50 μl contains 2× the desired final concentration.
[0121] Add 50 μl of compounds to the designated wells.
[0122] Scan the plate to check connections.
[0123] Run steps 3-1 and 3-2.
[0124] Step 3-1 sample every 2 minutes 30 times.
[0125] Step 3-2 sample every 15 minutes 100 times.
[0126] FIG. 2 shows a comparison of ACEA data for the indicated tight junction agonists.
Example 3
Assay of Cytoskeletal Rearrangement Induced by Tight Junction Agonists
[0127] Gliadin treated with the peptidases pepsin and trypsin (termed PT-gliadin or PTG) induces a cytoskeletal arrangement in CaCo2 cells grown in monolayers. The rearrangement can be visualized using a Nikon-TE2000 epifluorescence microscope and a 40× objective and Alexa Fluor 555 conjugated phalloidin (Invitrogen, Carlsbad, Calif.), which binds specifically to F-actin. Exposure times were identical for control and agonist treated samples. The figures were generated using Adobe Photoshop CS2 v 9.0.2. The concentration of agonist was as indicated. Tight junction agonists can be identified by their ability to induce the cytoskeletal rearrangement as shown by the effects of peptide FCIGRL, a known tight junction agonist. FIGS. 3-6 and 8-11 show the cytoskeletal rearrangements induced by exemplary tight junction agonists of the invention, including with respect to the distribution of F-actin and the tight junction protein ZO-1.
[0128] Additional results are provided in the following tables. The first column of the table provides SEQ ID NO: of the peptide, the second column provides the sequence of the peptides tested, the third column provides the results of the indicated assay (i.e., ACEA, TEER reduction, or Lucifer Yellow flux).
[0129] In the following tables + indicates an enhancement of the permeability of the tight junctions were observed and - indicates no enhancement of permeability was observed.
TABLE-US-00001 TABLE 1 Amino acid substitutions at position 2 of SEQ ID NO: l. SEQ Enhanced ID LY Reduced NO: Sequence permeability TEER 1 Phe-Cys-Ile-Gly-Arg-Leu + + 2 Phe-AllylGly-Ile-Gly-Arg-Leu-OH + + 3 Phe-AllylGly-Ile-Gly-Arg-NH2 - - 4 Phe-(d)AllylGly-Ile-Gly-Arg-NH2 - -
TABLE-US-00002 TABLE 2 Amino acid substitutions at position 1 of SEQ ID NO: 2. SEQ Enhanced ID LY Reduced NO: Sequence permeability TEER 1 Phe-Cys-Ile-Gly-Arg-Leu + + 5 Met-AllylGly-Ile-Gly-Arg-Leu-NH2 + - 6 Gln-AllylGly-Ile-Gly-Arg-Leu-NH2 - - 7 Leu-AllylGly-Ile-Gly-Arg-Leu-NH2 + - 8 Ser-AllylGly-Ile-Gly-Arg-Leu-NH2 - - 9 Thr-AllylGly-Ile-Gly-Arg-Leu-NH2 - - 10 Glu-AllylGly-Ile-Gly-Arg-Leu-NH2 - - 11 Val-AllylGly-Ile-Gly-Arg-Leu-NH2 - - 12 Tyr-AllylGly-Ile-Gly-Arg-Leu-NH2 - - 13 Gly-AllylGly-Ile-Gly-Arg-Leu-NH2 - - 14 Asp-AllylGly-Ile-Gly-Arg-Leu-NH2 - - 15 Trp-AllylGly-Ile-Gly-Arg-Leu-NH2 + - 16 Lys-AllylGly-Ile-Gly-Arg-Leu-NH2 - - 17 Ala-AllylGly-Ile-Gly-Arg-Leu-NH2 - - 18 His-AllylGly-Ile-Gly-Arg-Leu-NH2 - - 19 Pro-AllylGly-Ile-Gly-Arg-Leu-NH2 - - 20 Arg-AllylGly-Ile-Gly-Arg-Leu-NH2 + - 21 Ile-AllylGly-Ile-Gly-Arg-Leu-NH2 - -
TABLE-US-00003 TABLE 3 Amino acid substitutions at position 3 of SEQ ID NO: 2. SEQ Enhanced ID LY Reduced NO: Sequence permeability TEER 1 Phe-Cys-Ile-Gly-Arg-Leu + + 22 Phe-AllylGly-Pro-Gly-Arg-Leu-NH2 - - 23 Phe-AllylGly-Phe-Gly-Arg-Leu-NH2 + + 24 Phe-AllylGly-Thr-Gly-Arg-Leu-NH2 - - 25 Phe-AllylGly-Leu-Gly-Arg-Leu-NH2 + + 26 Phe-AllylGly-Ser-Gly-Arg-Leu-NH2 + + 27 Phe-AllylGly-Phe-Gly-Arg-Leu-NH2 + + 28 Phe-AllylGly-Val-Gly-Arg-Leu-NH2 - - 29 Phe-AllylGly-Gly-Gly-Arg-Leu-NH2 + + 30 Phe-AllylGly-Ala-Gly-Arg-Leu-NH2 + + 31 Phe-AllylGly-His-Gly-Arg-Leu-NH2 + + 32 Phe-AllylGly-Asp-Gly-Arg-Leu-NH2 + + 33 Phe-AllylGly-Glu-Gly-Arg-Leu-NH2 + + 34 Phe-AllylGly-Gln-Gly-Arg-Leu-NH2 + + 35 Phe-AllylGly-Arg-Gly-Arg-Leu-NH2 + + 36 Phe-AllylGly-Lys-Gly-Arg-Leu-NH2 + + 37 Phe-AllylGly-Asn-Gly-Arg-Leu-NH2 + + 38 Phe-AllylGly-Tyr-Gly-Arg-Leu-NH2 + +
TABLE-US-00004 TABLE 4 Amino acid substitutions at position 4 of SEQ ID NO: 2. SEQ Enhanced ID LY Reduced NO: Sequence permeability TEER 1 Phe-Cys-Ile-Gly-Arg-Leu + + 39 Phe-AllylGly-Ile-Thr-Arg-Leu-NH2 + + 40 Phe-AllylGly-Ile-Leu-Arg-Leu-NH2 41 Phe-AllylGly-Ile-Ile-Arg-Leu-NH2 42 Phe-AllylGly-Ile-Ala-Arg-Leu-NH2 + + 43 Phe-AllylGly-Ile-Pro-Arg-Leu-NH2 - - 44 Phe-AllylGly-Ile-Gly-Arg-Leu-NH2 45 Phe-AllylGly-Ile-His-Arg-Leu-NH2 + + 46 Phe-AllylGly-Ile-Asp-Arg-Leu-NH2 + + 47 Phe-AllylGly-Ile-Glu-Arg-Leu-NH2 + + 48 Phe-AllylGly-Ile-Gln-Arg-Leu-NH2 + + 49 Phe-AllylGly-Ile-Phe-Arg-Leu-NH2 + + 50 Phe-AllylGly-Ile-Arg-Arg-Leu-NH2 51 Phe-AllylGly-Ile-Lys-Arg-Leu-NH2 - - 52 Phe-AllylGly-Ile-Asn-Arg-Leu-NH2 + + 53 Phe-AllylGly-Ile-Ser-Arg-Leu-NH2 + + 54 Phe-AllylGly-Ile-Val-Arg-Leu-NH2 - +
TABLE-US-00005 TABLE 5 Amino acid substitutions at position 5 of SEQ ID NO: 2. SEQ Enhanced ID LY Reduced NO: Sequence permeability TEER 1 Phe-Cys-Ile-Gly-Arg-Leu + + 55 Phe-AllylGly-Ile-Gly-His-Leu-NH2 - - 56 Phe-AllylGly-Ile-Gly-Asp-Leu-NH2 + + 57 Phe-AllylGly-Ile-Gly-Glu-Leu-NH2 - - 58 Phe-AllylGly-Ile-Gly-Gln-Leu-NH2 - - 59 Phe-AllylGly-Ile-Gly-Gly-Leu-NH2 + + 60 Phe-AllylGly-Ile-Gly-Ala-Leu-NH2 + 61 Phe-AllylGly-Ile-Gly-Phe-Leu-NH2 62 Phe-AllylGly-Ile-Gly-Lys-Leu-NH2 + + 63 Phe-AllylGly-Ile-Gly-Leu-Leu-NH2 64 Phe-AllylGly-Ile-Gly-Met-Leu-NH2 65 Phe-AllylGly-Ile-Gly-Asn-Leu-NH2 66 Phe-AllylGly-Ile-Gly-Ser-Leu-NH2 67 Phe-AllylGly-Ile-Gly-Tyr-Leu-NH2 68 Phe-AllylGly-Ile-Gly-Thr-Leu-NH2 + 69 Phe-AllylGly-Ile-Gly-Ile-Leu-NH2 - 70 Phe-AllylGly-Ile-Gly-Trp-Leu-NH2 + + 71 Phe-AllylGly-Ile-Gly-Pro-Leu-NH2 + - 72 Phe-AllylGly-Ile-Gly-Val-Leu-NH2 - +
TABLE-US-00006 TABLE 6 Amino acid substitutions at position 6 of SEQ ID NO: 2. SEQ Enhanced ID LY Reduced NO: Sequence permeability TEER 1 Phe-Cys-Ile-Gly-Arg-Leu + + 73 Phe-AllylGly-Ile-Gly-Arg-His-NH2 + + 74 Phe-AllylGly-Ile-Gly-Arg-Asp-NH2 + + 75 Phe-AllylGly-Ile-Gly-Arg-Arg-NH2 + - 76 Phe-AllylGly-Ile-Gly-Arg-Phe-NH2 + + 77 Phe-AllylGly-Ile-Gly-Arg-Ala-NH2 + - 78 Phe-AllylGly-Ile-Gly-Arg-Gly-NH2 + - 79 Phe-AllylGly-Ile-Gly-Arg-Gln-NH2 - - 80 Phe-AllylGly-Ile-Gly-Arg-Glu-NH2 + + 81 Phe-AllylGly-Ile-Gly-Arg-Thr-NH2 - + 82 Phe-AllylGly-Ile-Gly-Arg-Tyr-NH2 + + 83 Phe-AllylGly-Ile-Gly-Arg-Ser-NH2 - - 84 Phe-AllylGly-Ile-Gly-Arg-Asn-NH2 + + 85 Phe-AllylGly-Ile-Gly-Arg-Met-NH2 + + 86 Phe-AllylGly-Ile-Gly-Arg-Lys-NH2 + - 87 Phe-AllylGly-Ile-Gly-Arg-Ile-NH2 + + 88 Phe-AllylGly-Ile-Gly-Arg-Trp-NH2 + + 89 Phe-Allylaly-Ile-Gly-Arg-Pro-NH2 - - 90 Phe-AllylGly-Ile-Gly-Arg-Val-NH2 + +
TABLE-US-00007 TABLE 7 Abbreviations and Structures of Non-Naturally Occurring Amino Acids. Abbreviation IUPAC Name Chemical Structure Sar Sarcosine ##STR00001## Aib alpha-aminoisobutyric acid ##STR00002## Tle L-tert-Leucine ##STR00003## MeAla L-N-methyl Alanine ##STR00004## Abu L-alpha-aminobutyric acid ##STR00005## Phe(4-NO2) L-4-nitro-phenylalanine ##STR00006## Phe(4-Cl) L-4-chlorophenylalanine ##STR00007## Tic L-1,2,3,4-tetrahydroisoquinoline-3- carboxylic acid ##STR00008## Thi L-beta-(2-thienyl)-alanine ##STR00009## Met(O) L-methionine-sulfoxide ##STR00010## Met(O)2 L-methionine-sulfone ##STR00011## Nle L-norleucine ##STR00012## Cys(S-benzyl) L-S-benzyl-cysteine ##STR00013## Cys(t-buthiol) L-S-tert-butylthio-cysteine ##STR00014## Phg L-phenylglycine ##STR00015## Cha L-beta-cyclohexyl-alanine ##STR00016## (Allyl)Gly L-allylglycine ##STR00017## (t-Bu)Gly L-tert-butylglycine ##STR00018## Dab L-1,4-diaminobutyric acid ##STR00019## (cyclopropane)Pro L-(R,S)-3,4-cis-methanoproline ##STR00020## Dap/Dpr L-1,3-diaminopropionic acid ##STR00021## Pen(Acm) L-S-acetamidomethyl-penicillamine ##STR00022## (2-pyridyl)Ala L-beta-(2-pyridyl)-alanine ##STR00023## (4, 5-dehydro)Leu L-4,5-dehydro-leucine ##STR00024## Phe(4-CN) L-4-cyano-phenylalanine ##STR00025## Phe(3-Me) L-3-methyl-phenylalanine ##STR00026## (cyclopropyl)Ala L-beta-cyclopropyl-alanine ##STR00027## Pra L-propargylglycine ##STR00028## (2-furyl)Ala L-beta-(2-furyl)-alanine ##STR00029## Thh 1,2,3,4-tetrahydroharmane-3- carboxylic acid ##STR00030## (styryl)Gly L-beta-styryl-alanine ##STR00031## HOCit Homocitrulline ##STR00032##
[0130] All publications, patents and patent applications mentioned in this specification are indicative of the level of skill of those skilled in the art to which this invention pertains, and 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.
Sequence CWU
1
1
27416PRTUnknownPeptide tight junction agonist 1Phe Cys Ile Gly Arg Leu 1
5 26PRTUnknownPeptide tight junction agonist 2Phe Xaa
Ile Gly Arg Leu 1 5 35PRTUnknownPeptide tight
junction agonist 3Phe Xaa Ile Gly Arg 1 5
45PRTUnknownPeptide tight junction agonist 4Phe Xaa Ile Gly Arg 1
5 56PRTUnknownPeptide tight junction agonist 5Met Xaa Ile Gly Arg
Leu 1 5 66PRTUnknownPeptide tight junction agonist
6Gln Xaa Ile Gly Arg Leu 1 5 76PRTUnknownPeptide
tight junction agonist 7Leu Xaa Ile Gly Arg Leu 1 5
86PRTUnknownPeptide tight junction agonist 8Ser Xaa Ile Gly Arg Leu 1
5 96PRTUnknownPeptide tight junction agonist 9Thr Xaa Ile
Gly Arg Leu 1 5 106PRTUnknownPeptide tight junction
agonist 10Glu Xaa Ile Gly Arg Leu 1 5
116PRTUnknownPeptide tight junction agonist 11Val Xaa Ile Gly Arg Leu 1
5 126PRTUnknownPeptide tight junction agonist 12Tyr Xaa
Ile Gly Arg Leu 1 5 136PRTUnknownPeptide tight
junction agonist 13Gly Xaa Ile Gly Arg Leu 1 5
146PRTUnknownPeptide tight junction agonist 14Asp Xaa Ile Gly Arg Leu 1
5 156PRTUnknownPeptide tight junction agonist 15Trp Xaa
Ile Gly Arg Leu 1 5 166PRTUnknownPeptide tight
junction agonist 16Lys Xaa Ile Gly Arg Leu 1 5
176PRTUnknownPeptide tight junction agonist 17Ala Xaa Ile Gly Arg Leu 1
5 186PRTUnknownPeptide tight junction agonist 18His Xaa
Ile Gly Arg Leu 1 5 196PRTUnknownPeptide tight
junction agonist 19Pro Xaa Ile Gly Arg Leu 1 5
206PRTUnknownPeptide tight junction agonist 20Arg Xaa Ile Gly Arg Leu 1
5 216PRTUnknownPeptide tight junction agonist 21Ile Xaa
Ile Gly Arg Leu 1 5 226PRTUnknownPeptide tight
junction agonist 22Phe Xaa Pro Gly Arg Leu 1 5
236PRTUnknownPeptide tight junction agonist 23Phe Xaa Phe Gly Arg Leu 1
5 246PRTUnknownPeptide tight junction agonist 24Phe Xaa
Thr Gly Arg Leu 1 5 256PRTUnknownPeptide tight
junction agonist 25Phe Xaa Leu Gly Arg Leu 1 5
266PRTUnknownPeptide tight junction agonist 26Phe Xaa Ser Gly Arg Leu 1
5 276PRTUnknownPeptide tight junction agonist 27Phe Xaa
Phe Gly Arg Leu 1 5 286PRTUnknownPeptide tight
junction agonist 28Phe Xaa Val Gly Arg Leu 1 5
296PRTUnknownPeptide tight junction agonist 29Phe Xaa Gly Gly Arg Leu 1
5 306PRTUnknownPeptide tight junction agonist 30Phe Xaa
Ala Gly Arg Leu 1 5 316PRTUnknownPeptide tight
junction agonist 31Phe Xaa His Gly Arg Leu 1 5
326PRTUnknownPeptide tight junction agonist 32Phe Xaa Asp Gly Arg Leu 1
5 336PRTUnknownPeptide tight junction agonist 33Phe Xaa
Glu Gly Arg Leu 1 5 346PRTUnknownPeptide tight
junction agonist 34Phe Xaa Gln Gly Arg Leu 1 5
356PRTUnknownPeptide tight junction agonist 35Phe Xaa Arg Gly Arg Leu 1
5 366PRTUnknownPeptide tight junction agonist 36Phe Xaa
Lys Gly Arg Leu 1 5 376PRTUnknownPeptide tight
junction agonist 37Phe Xaa Asn Gly Arg Leu 1 5
386PRTUnknownPeptide tight junction agonist 38Phe Xaa Tyr Gly Arg Leu 1
5 396PRTUnknownPeptide tight junction agonist 39Phe Xaa
Ile Thr Arg Leu 1 5 406PRTUnknownPeptide tight
junction agonist 40Phe Xaa Ile Leu Arg Leu 1 5
416PRTUnknownPeptide tight junction agonist 41Phe Xaa Ile Ile Arg Leu 1
5 426PRTUnknownPeptide tight junction agonist 42Phe Xaa
Ile Ala Arg Leu 1 5 436PRTUnknownPeptide tight
junction agonist 43Phe Xaa Ile Pro Arg Leu 1 5
446PRTUnknownPeptide tight junction agonist 44Phe Xaa Ile Gly Arg Leu 1
5 456PRTUnknownPeptide tight junction agonist 45Phe Xaa
Ile His Arg Leu 1 5 466PRTUnknownPeptide tight
junction agonist 46Phe Xaa Ile Asp Arg Leu 1 5
476PRTUnknownPeptide tight junction agonist 47Phe Xaa Ile Glu Arg Leu 1
5 486PRTUnknownPeptide tight junction agonist 48Phe Xaa
Ile Gln Arg Leu 1 5 496PRTUnknownPeptide tight
junction agonist 49Phe Xaa Ile Phe Arg Leu 1 5
506PRTUnknownPeptide tight junction agonist 50Phe Xaa Ile Arg Arg Leu 1
5 516PRTUnknownPeptide tight junction agonist 51Phe Xaa
Ile Lys Arg Leu 1 5 526PRTUnknownPeptide tight
junction agonist 52Phe Xaa Ile Asn Arg Leu 1 5
536PRTUnknownPeptide tight junction agonist 53Phe Xaa Ile Ser Arg Leu 1
5 546PRTUnknownPeptide tight junction agonist 54Phe Xaa
Ile Val Arg Leu 1 5 556PRTUnknownPeptide tight
junction agonist 55Phe Xaa Ile Gly His Leu 1 5
566PRTUnknownPeptide tight junction agonist 56Phe Xaa Ile Gly Asp Leu 1
5 576PRTUnknownPeptide tight junction agonist 57Phe Xaa
Ile Gly Glu Leu 1 5 586PRTUnknownPeptide tight
junction agonist 58Phe Xaa Ile Gly Gln Leu 1 5
596PRTUnknownPeptide tight junction agonist 59Phe Xaa Ile Gly Gly Leu 1
5 606PRTUnknownPeptide tight junction agonist 60Phe Xaa
Ile Gly Ala Leu 1 5 616PRTUnknownPeptide tight
junction agonist 61Phe Xaa Ile Gly Phe Leu 1 5
626PRTUnknownPeptide tight junction agonist 62Phe Xaa Ile Gly Lys Leu 1
5 636PRTUnknownPeptide tight junction agonist 63Phe Xaa
Ile Gly Leu Leu 1 5 646PRTUnknownPeptide tight
junction agonist 64Phe Xaa Ile Gly Met Leu 1 5
656PRTUnknownPeptide tight junction agonist 65Phe Xaa Ile Gly Asn Leu 1
5 666PRTUnknownPeptide tight junction agonist 66Phe Xaa
Ile Gly Ser Leu 1 5 676PRTUnknownPeptide tight
junction agonist 67Phe Xaa Ile Gly Tyr Leu 1 5
686PRTUnknownPeptide tight junction agonist 68Phe Xaa Ile Gly Thr Leu 1
5 696PRTUnknownPeptide tight junction agonist 69Phe Xaa
Ile Gly Ile Leu 1 5 706PRTUnknownPeptide tight
junction agonist 70Phe Xaa Ile Gly Trp Leu 1 5
716PRTUnknownPeptide tight junction agonist 71Phe Xaa Ile Gly Pro Leu 1
5 726PRTUnknownPeptide tight junction agonist 72Phe Xaa
Ile Gly Val Leu 1 5 736PRTUnknownPeptide tight
junction agonist 73Phe Xaa Ile Gly Arg His 1 5
746PRTUnknownPeptide tight junction agonist 74Phe Xaa Ile Gly Arg Asp 1
5 756PRTUnknownPeptide tight junction agonist 75Phe Xaa
Ile Gly Arg Arg 1 5 766PRTUnknownPeptide tight
junction agonist 76Phe Xaa Ile Gly Arg Phe 1 5
776PRTUnknownPeptide tight junction agonist 77Phe Xaa Ile Gly Arg Ala 1
5 786PRTUnknownPeptide tight junction agonist 78Phe Xaa
Ile Gly Arg Gly 1 5 796PRTUnknownPeptide tight
junction agonist 79Phe Xaa Ile Gly Arg Gln 1 5
806PRTUnknownPeptide tight junction agonist 80Phe Xaa Ile Gly Arg Glu 1
5 816PRTUnknownPeptide tight junction agonist 81Phe Xaa
Ile Gly Arg Thr 1 5 826PRTUnknownPeptide tight
junction agonist 82Phe Xaa Ile Gly Arg Tyr 1 5
836PRTUnknownPeptide tight junction agonist 83Phe Xaa Ile Gly Arg Ser 1
5 846PRTUnknownPeptide tight junction agonist 84Phe Xaa
Ile Gly Arg Asn 1 5 856PRTUnknownPeptide tight
junction agonist 85Phe Xaa Ile Gly Arg Met 1 5
866PRTUnknownPeptide tight junction agonist 86Phe Xaa Ile Gly Arg Lys 1
5 876PRTUnknownPeptide tight junction agonist 87Phe Xaa
Ile Gly Arg Ile 1 5 886PRTUnknownPeptide tight
junction agonist 88Phe Xaa Ile Gly Arg Trp 1 5
896PRTUnknownPeptide tight junction agonist 89Phe Xaa Ile Gly Arg Pro 1
5 906PRTUnknownPeptide tight junction agonist 90Phe Xaa
Ile Gly Arg Val 1 5 916PRTUnknownPeptide tight
junction agonist 91Phe Cys Ile Gly Arg Leu 1 5
926PRTUnknownPeptide tight junction agonist 92Phe Thr Ile Gly Arg Leu 1
5 936PRTUnknownPeptide tight junction agonist 93Phe Ser
Ile Gly Arg Leu 1 5 946PRTUnknownPeptide tight
junction agonist 94Phe Met Ile Gly Arg Leu 1 5
956PRTUnknownPeptide tight junction agonist 95Phe Leu Ile Gly Arg Leu 1
5 967PRTUnknownPeptide tight junction agonist 96Phe Phe
Leu Ile Gly Arg Leu 1 5 976PRTUnknownPeptide
tight junction agonist 97Phe Phe Ile Gly Arg Leu 1 5
986PRTUnknownPeptide tight junction agonist 98Phe Pro Ile Gly Arg Leu 1
5 996PRTUnknownPeptide tight junction agonist 99Phe Trp
Ile Gly Arg Leu 1 5 1006PRTUnknownPeptide tight
junction agonist 100Phe His Ile Gly Arg Leu 1 5
1016PRTUnknownPeptide tight junction agonist 101Phe Pro Ile Gly Arg Leu 1
5 1026PRTUnknownPeptide tight junction agonist 102Phe
Asp Ile Gly Arg Leu 1 5 1036PRTUnknownPeptide tight
junction agonist 103Phe Leu Ile Gly Arg Leu 1 5
1046PRTUnknownPeptide tight junction agonist 104Phe Phe Ile Gly Arg Leu 1
5 1056PRTUnknownPeptide tight junction agonist 105Phe
Arg Ile Gly Arg Leu 1 5 1066PRTUnknownPeptide tight
junction agonist 106Phe Gly Ile Gly Arg Leu 1 5
1076PRTUnknownPeptide tight junction agonist 107Phe Gln Ile Gly Arg Leu 1
5 1086PRTUnknownPeptide tight junction agonist 108Phe
Glu Ile Gly Arg Leu 1 5 1096PRTUnknownPeptide tight
junction agonist 109Phe Lys Ile Gly Arg Leu 1 5
1106PRTUnknownPeptide tight junction agonist 110Phe Asn Ile Gly Arg Leu 1
5 1116PRTUnknownPeptide tight junction agonist 111Phe
Tyr Ile Gly Arg Leu 1 5 1126PRTUnknownPeptide tight
junction agonist 112Phe Leu Ile Gly Arg Leu 1 5
1136PRTUnknownPeptide tight junction agonist 113Phe Val Ile Gly Arg Leu 1
5 1146PRTUnknownPeptide tight junction agonist 114Phe
Ile Ile Gly Arg Leu 1 5 1156PRTUnknownPeptide tight
junction agonist 115Ser Leu Ile Gly Arg Leu 1 5
1166PRTUnknownPeptide tight junction agonist 116Leu Arg Gly Ile Leu Phe 1
5 1175PRTUnknownPeptide tight junction agonist 117Phe
Leu Ile Gly Arg 1 5 1186PRTUnknownPeptide tight junction
agonist 118Phe Xaa Ile Gly Arg Leu 1 5
1196PRTUnknownPeptide tight junction agonist 119Phe Xaa Ile Gly Arg Leu 1
5 1206PRTUnknownPeptide tight junction agonist 120Phe
Xaa Ile Gly Arg Leu 1 5 1216PRTUnknownPeptide tight
junction agonist 121Phe Xaa Ile Gly Arg Leu 1 5
1226PRTUnknownPeptide tight junction agonist 122Phe Xaa Ile Gly Arg Leu 1
5 1236PRTUnknownPeptide tight junction agonist 123Phe
Cys Ile Gly Arg Leu 1 5 1246PRTUnknownPeptide tight
junction agonist 124Phe Xaa Ile Gly Arg Leu 1 5
1256PRTUnknownPeptide tight junction agonist 125Phe Xaa Ile Gly Arg Leu 1
5 1266PRTUnknownPeptide tight junction agonist 126Phe
Xaa Ile Gly Arg Ala 1 5 1276PRTUnknownPeptide tight
junction agonist 127Phe Xaa Ile Gly Arg Ser 1 5
1286PRTUnknownPeptide tight junction agonist 128Phe Xaa Ile Gly Arg Phe 1
5 1296PRTUnknownPeptide tight junction agonist 129Phe
Xaa Ile Gly Arg Phe 1 5 1306PRTUnknownPeptide tight
junction agonist 130Phe Xaa Ile Gly Arg Leu 1 5
1316PRTUnknownPeptide tight junction agonist 131Phe Xaa Ile Gly Arg Leu 1
5 1326PRTUnknownPeptide tight junction agonist 132Phe
Xaa Ile Gly Arg Leu 1 5 1336PRTUnknownPeptide tight
junction agonist 133Phe Val Ile Gly Arg Leu 1 5
1346PRTUnknownPeptide tight junction agonist 134Phe Xaa Ile Gly Arg Leu 1
5 1356PRTUnknownPeptide tight junction agonist 135Phe
Xaa Ile Gly Arg Leu 1 5 1366PRTUnknownPeptide tight
junction agonist 136Phe Xaa Ile Gly Arg Leu 1 5
1376PRTUnknownPeptide tight junction agonist 137Phe Xaa Ile Gly Arg Leu 1
5 1386PRTUnknownPeptide tight junction agonist 138Phe
Xaa Ile Gly Arg Leu 1 5 1396PRTUnknownPeptide tight
junction agonist 139Phe Xaa Ile Gly Arg Leu 1 5
1406PRTUnknownPeptide tight junction agonist 140Phe Xaa Ile Gly Arg Leu 1
5 1416PRTUnknownPeptide tight junction agonist 141Phe
Xaa Ile Gly Arg Leu 1 5 1426PRTUnknownPeptide tight
junction agonist 142Phe Leu Ile Gly Arg Leu 1 5
1436PRTUnknownPeptide tight junction agonist 143Phe Leu Ile Gly Arg Leu 1
5 1446PRTUnknownPeptide tight junction agonist 144Leu
Arg Gly Ile Leu Phe 1 5 1456PRTUnknownPeptide tight
junction agonist 145Phe Xaa Ile Gly Arg Leu 1 5
1466PRTUnknownPeptide tight junction agonist 146Phe Xaa Ile Gly Arg Leu 1
5 1475PRTUnknownPeptide tight junction agonist 147Phe
Xaa Ile Gly Arg 1 5 1485PRTUnknownPeptide tight junction
agonist 148Phe Xaa Ile Gly Arg 1 5 1496PRTUnknownPeptide
tight junction agonist 149Phe Xaa Ile Gly Arg Leu 1 5
1506PRTUnknownPeptide tight junction agonist 150Phe Xaa Ile Gly Arg Leu 1
5 1516PRTUnknownPeptide tight junction agonist 151Xaa
Phe Ile Gly Arg Leu 1 5 1526PRTUnknownPeptide tight
junction agonist 152Xaa Phe Ile Gly Arg Leu 1 5
1536PRTUnknownPeptide tight junction agonist 153Phe Xaa Ile Gly Arg Leu 1
5 1545PRTUnknownPeptide tight junction agonist 154Phe
Xaa Ile Gly Arg 1 5 1555PRTUnknownPeptide tight junction
agonist 155Phe Xaa Ile Gly Arg 1 5 1565PRTUnknownPeptide
tight junction agonist 156Phe Xaa Ile Gly Arg 1 5
1576PRTUnknownPeptide tight junction agonist 157Phe Xaa Ile Gly Arg Leu 1
5 1586PRTUnknownPeptide tight junction agonist 158Phe
Xaa Ile Gly Arg Leu 1 5 1596PRTUnknownPeptide tight
junction agonist 159Phe Xaa Ile Gly Arg Leu 1 5
1606PRTUnknownPeptide tight junction agonist 160Phe Xaa Ile Gly Arg Leu 1
5 1616PRTUnknownPeptide tight junction agonist 161Phe
Cys Ile Gly Arg Leu 1 5 1626PRTUnknownPeptide tight
junction agonist 162Phe Cys Ala Gly Met Ser 1 5
1636PRTUnknownPeptide tight junction agonist 163Phe Cys Val Gly Met Ser 1
5 1646PRTUnknownPeptide tight junction agonist 164Pro
Cys Ile Gly Arg Leu 1 5 1656PRTUnknownPeptide tight
junction agonist 165Gln Cys Ile Gly Arg Leu 1 5
1666PRTUnknownPeptide tight junction agonist 166Gly Cys Ile Gly Arg Leu 1
5 1676PRTUnknownPeptide tight junction agonist 167Thr
Cys Ile Gly Arg Leu 1 5 1686PRTUnknownPeptide tight
junction agonist 168Ser Cys Ile Gly Arg Leu 1 5
1696PRTUnknownPeptide tight junction agonist 169Asn Cys Ile Gly Arg Leu 1
5 1706PRTUnknownPeptide tight junction agonist 170Arg
Cys Ile Gly Arg Leu 1 5 1716PRTUnknownPeptide tight
junction agonist 171Val Cys Ile Gly Arg Leu 1 5
1726PRTUnknownPeptide tight junction agonist 172Phe Cys Ile Gly Arg Gly 1
5 1736PRTUnknownPeptide tight junction agonist 173Ala
Cys Ile Gly Arg Gly 1 5 1746PRTUnknownPeptide tight
junction agonist 174Ala Cys Ile Gly Arg Gly 1 5
1756PRTUnknownPeptide tight junction agonist 175Phe Cys Ile Gly Arg Gly 1
5 1766PRTUnknownPeptide tight junction agonist 176Phe
Cys Ile Gly Arg Gly 1 5 1776PRTUnknownPeptide tight
junction agonist 177Phe Cys Ile Gly Arg Ser 1 5
1786PRTUnknownPeptide tight junction agonist 178Phe Cys Ile Gly Arg Gln 1
5 1796PRTUnknownPeptide tight junction agonist 179Phe
Cys Ile Gly Arg Lys 1 5 1806PRTUnknownPeptide tight
junction agonist 180Phe Cys Ile Gly Arg Ala 1 5
1816PRTUnknownPeptide tight junction agonist 181Phe Cys Ile Gly Arg Ile 1
5 1826PRTUnknownPeptide tight junction agonist 182Phe
Cys Ile Gly Arg Gly 1 5 1836PRTUnknownPeptide tight
junction agonist 183Phe Cys Ile Gly Arg Asp 1 5
1846PRTUnknownPeptide tight junction agonist 184Phe Cys Ile Gly Arg Glu 1
5 1856PRTUnknownPeptide tight junction agonist 185Phe
Cys Ile Gly Arg Phe 1 5 1866PRTUnknownPeptide tight
junction agonist 186Phe Cys Ile Gly Arg Asn 1 5
1876PRTUnknownPeptide tight junction agonist 187Phe Cys Ile Gly Arg Pro 1
5 1886PRTUnknownPeptide tight junction agonist 188Glu
Cys Ile Gly Arg Leu 1 5 1896PRTUnknownPeptide tight
junction agonist 189Asp Cys Ile Gly Arg Leu 1 5
1906PRTUnknownPeptide tight junction agonist 190Lys Cys Ile Gly Arg Leu 1
5 1917PRTUnknownPeptide tight junction agonist 191Phe
Cys Ile Gly Arg Leu Cys 1 5 1926PRTUnknownPeptide
tight junction agonist 192Pro Gly Pro Gly Arg Leu 1 5
1936PRTUnknownPeptide tight junction agonist 193Phe Cys Ile Pro Gly Pro 1
5 1946PRTUnknownPeptide tight junction agonist 194Phe
Cys Leu Gly Arg Leu 1 5 1956PRTUnknownPeptide tight
junction agonist 195Gly Cys Ile Gly Arg Gly 1 5
1966PRTUnknownPeptide tight junction agonist 196Tyr Cys Ile Gly Arg Leu 1
5 1976PRTUnknownPeptide tight junction agonist 197Ala
Cys Ile Gly Arg Leu 1 5 1986PRTUnknownPeptide tight
junction agonist 198Trp Cys Ile Gly Arg Leu 1 5
1996PRTUnknownPeptide tight junction agonist 199Ala Cys Ile Gly Arg Ser 1
5 2006PRTUnknownPeptide tight junction agonist 200Ala
Cys Ile Gly Arg Ala 1 5 2016PRTUnknownPeptide tight
junction agonist 201Phe Cys Ile Gly Arg Phe 1 5
2026PRTUnknownPeptide tight junction agonist 202Ser Leu Ile Gly Arg Leu 1
5 2034PRTUnknownPeptide tight junction agonist 203Phe
Cys Ala Gly 1 2044PRTUnknownPeptide tight junction agonist
204Phe Cys Gly Gly 1 2057PRTUnknownPeptide tight junction
agonist 205Gly Phe Cys Ile Gly Arg Leu 1 5
2066PRTUnknownPeptide tight junction agonist 206Leu Arg Gly Gly Arg Leu 1
5 2076PRTUnknownPeptide tight junction agonist 207Phe
Cys Ala Gly Met Ser 1 5 2086PRTUnknownPeptide tight
junction agonist 208Phe Cys Val Gly Met Ser 1 5
2096PRTUnknownPeptide tight junction agonist 209Phe Leu Ile Gly Arg Leu 1
5 2105PRTUnknownPeptide tight junction agonist 210Tyr
Ile Gly Ser Arg 1 5 2116PRTUnknownPeptide tight junction
agonist 211Xaa Cys Ile Gly Arg Leu 1 5
2126PRTUnknownPeptide tight junction agonist 212Xaa Cys Ile Gly Arg Leu 1
5 2136PRTUnknownPeptide tight junction agonist 213Xaa
Cys Ile Gly Arg Leu 1 5 2146PRTUnknownPeptide tight
junction agonist 214Xaa Cys Ile Gly Arg Leu 1 5
2156PRTUnknownPeptide tight junction agonist 215Xaa Cys Ile Gly Arg Leu 1
5 2166PRTUnknownPeptide tight junction agonist 216Xaa
Cys Ile Gly Arg Leu 1 5 2176PRTUnknownPeptide tight
junction agonist 217Phe Cys Ile Gly Arg Xaa 1 5
2186PRTUnknownPeptide tight junction agonist 218Phe Cys Ile Gly Arg Xaa 1
5 2196PRTUnknownPeptide tight junction agonist 219Phe
Cys Ile Gly Arg Xaa 1 5 2206PRTUnknownPeptide tight
junction agonist 220Phe Cys Ile Gly Arg Xaa 1 5
2216PRTUnknownPeptide tight junction agonist 221Phe Cys Ile Gly Arg Xaa 1
5 2226PRTUnknownPeptide tight junction agonist 222Phe
Cys Ile Gly Arg Xaa 1 5 2236PRTUnknownPeptide tight
junction agonist 223Phe Cys Ile Gly Arg Xaa 1 5
2246PRTUnknownPeptide tight junction agonist 224Xaa Cys Ile Gly Arg Leu 1
5 2256PRTUnknownPeptide tight junction agonist 225Xaa
Cys Ile Gly Arg Leu 1 5 2266PRTUnknownPeptide tight
junction agonist 226Phe Cys Ile Gly Xaa Leu 1 5
2276PRTUnknownPeptide tight junction agonist 227Xaa Cys Ile Gly Arg Leu 1
5 2286PRTUnknownPeptide tight junction agonist 228Xaa
Cys Ile Gly Arg Leu 1 5 2296PRTUnknownPeptide tight
junction agonist 229Phe Cys Ile Gly Arg Xaa 1 5
2306PRTUnknownPeptide tight junction agonist 230Phe Cys Ile Gly Arg Xaa 1
5 2316PRTUnknownPeptide tight junction agonist 231Xaa
Cys Ile Gly Arg Leu 1 5 2326PRTUnknownPeptide tight
junction agonist 232Phe Cys Xaa Gly Arg Leu 1 5
2336PRTUnknownPeptide tight junction agonist 233Phe Cys Ile Gly Arg Xaa 1
5 2346PRTUnknownPeptide tight junction agonist 234Xaa
Cys Ile Gly Arg Leu 1 5 2356PRTUnknownPeptide tight
junction agonist 235Phe Cys Ile Gly Arg Xaa 1 5
2366PRTUnknownPeptide tight junction agonist 236Phe Cys Ile Gly Arg Leu 1
5 2376PRTUnknownPeptide tight junction agonist 237Ala
Cys Ile Gly Arg Leu 1 5 2386PRTUnknownPeptide tight
junction agonist 238Phe Ala Ile Gly Arg Leu 1 5
2396PRTUnknownPeptide tight junction agonist 239Phe Cys Ala Gly Arg Leu 1
5 2406PRTUnknownPeptide tight junction agonist 240Phe
Cys Ile Ala Arg Leu 1 5 2416PRTUnknownPeptide tight
junction agonist 241Phe Cys Ile Gly Ala Leu 1 5
2426PRTUnknownPeptide tight junction agonist 242Phe Cys Ile Gly Arg Ala 1
5 2435PRTUnknownPeptide tight junction agonist 243Cys
Ile Gly Arg Leu 1 5 2444PRTUnknownPeptide tight junction
agonist 244Ile Gly Arg Leu 1 2455PRTUnknownPeptide tight
junction agonist 245Phe Cys Ile Gly Arg 1 5
2464PRTUnknownPeptide tight junction agonist 246Phe Cys Ile Gly 1
2476PRTUnknownPeptide tight junction agonist 247Phe Cys Ile Gly Arg
Leu 1 5 2486PRTUnknownPeptide tight junction agonist
248Phe Cys Ile Gly Arg Leu 1 5 2496PRTUnknownPeptide
tight junction agonist 249Phe Cys Ile Gly Arg Leu 1 5
2506PRTUnknownPeptide tight junction agonist 250Phe Cys Ile Gly Arg Leu 1
5 2516PRTUnknownPeptide tight junction agonist 251Phe
Cys Ile Gly Arg Leu 1 5 2526PRTUnknownPeptide tight
junction agonist 252Leu Arg Gly Ile Cys Phe 1 5
2536PRTUnknownPeptide tight junction agonist 253Leu Arg Gly Ile Cys Phe 1
5 2546PRTUnknownPeptide tight junction agonist 254Leu
Arg Gly Ile Cys Phe 1 5 2556PRTUnknownPeptide tight
junction agonist 255Leu Arg Gly Ile Cys Phe 1 5
2566PRTUnknownPeptide tight junction agonist 256Leu Arg Gly Ile Cys Phe 1
5 2576PRTUnknownPeptide tight junction agonist 257Leu
Arg Gly Ile Cys Phe 1 5 2586PRTUnknownPeptide tight
junction agonist 258Leu Arg Gly Ile Cys Phe 1 5
2596PRTUnknownPeptide tight junction agonist 259Leu Arg Gly Ile Cys Phe 1
5 2606PRTUnknownPeptide tight junction agonist 260Leu
Arg Gly Ile Cys Phe 1 5 2616PRTUnknownPeptide tight
junction agonist 261Leu Arg Gly Ile Cys Phe 1 5
2626PRTUnknownPeptide tight junction agonist 262Leu Arg Gly Ile Cys Phe 1
5 2636PRTUnknownPeptide tight junction agonist 263Leu
Arg Gly Ile Cys Phe 1 5 2646PRTUnknownPeptide tight
junction agonist 264Phe Cys Ile Gly Arg Leu 1 5
2656PRTUnknownPeptide tight junction agonist 265Phe Cys Ile Gly Arg Leu 1
5 2666PRTUnknownPeptide tight junction agonist 266Phe
Cys Ile Gly Arg Leu 1 5 2676PRTUnknownPeptide tight
junction agonist 267Phe Cys Ile Gly Arg Leu 1 5
2686PRTUnknownPeptide tight junction agonist 268Phe Cys Ile Gly Arg Leu 1
5 2696PRTUnknownPeptide tight junction agonist 269Phe
Cys Ile Gly Arg Leu 1 5 2706PRTUnknownPeptide tight
junction agonist 270Phe Cys Ile Gly Arg Leu 1 5
2716PRTUnknownPeptide tight junction agonist 271Leu Arg Gly Ile Cys Phe 1
5 2726PRTUnknownPeptide tight junction agonist 272Leu
Arg Gly Ile Cys Phe 1 5 2736PRTUnknownPeptide tight
junction agonist 273Leu Arg Gly Ile Cys Phe 1 5
2746PRTUnknownPeptide tight junction agonist 274Leu Arg Gly Ile Cys Phe 1
5
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