Claudin-4 binding peptides, compositions and methods of use
View Patent ↗The disclosure provides methods and compositions useful for treating claudin-4 associated disorders including cell proliferative disorders. The disclosure also provide claudin-family binding peptides useful in the methods of the disclosure.
1. A substantially purified peptide consisting of a sequence selected from the group consisting of:
(a) NSSYSGNYPYSILFQKF;
(SEQ ID NO: 5)
(b) SSYSGNYPYSIL;
(SEQ ID NO: 6)
(c) NSSYSGNYYSIL; and
(SEQ ID NO: 7)
(d) APWTEHSYYLSL
(SEQ ID NO: 10).
2. The substantially purified peptide of claim 1 , wherein the peptide binds to a claudin-4 polypeptide.
3. The substantially purified peptide of claim 1 further comprising a moiety of interest linked to the peptide.
4. The substantially purified peptide of claim 3 , wherein the moiety of interest is a small molecule drug, a polypeptide or peptide, an antibody, a peptidomimetic, or a nanoparticle.
5. The substantially purified peptide of claim 4 , wherein the polypeptide or peptide is an immunogenic polypeptide or peptide.
6. The substantially purified peptide of claim 4 , wherein the polypeptide or peptide is a therapeutic polypeptide or peptide.
7. The substantially purified peptide of claim 4 , wherein the polypeptide or peptide is a growth factor.
8. The substantially purified peptide of claim 4 , wherein the small molecule drug is an anticancer drug.
9. The substantially purified peptide of claim 4 , wherein the nanoparticle is a metallic nanoparticle.
10. The substantially purified peptide of claim 4 , wherein the nanoparticle is a biocompatible polymer.
11. The substantially purified peptide of claim 10 , wherein the biocompatible polymer is poly(lactide-co-glycolide) (PLGA).
12. The substantially purified peptide of claim 11 , wherein the nanoparticle comprising PLGA further comprises a therapeutic agent.
13. A substantially purified peptide consisting of a sequence selected from the group consisting of:
(a) NSSYSGNYPYSILFQKF;
(SEQ ID NO: 5)
(b) SSYSGNYPYSIL;
(SEQ ID NO: 6)
(c) NSSYSGNYYSIL; and
(SEQ ID NO: 7)
(d) APWTEHSYYLSL
(SEQ ID NO: 10),
wherein the peptide comprises at least one D-amino acid.
14. A pharmaceutical composition comprising the peptide of claim 1 or 13 .
15. The composition of claim 14 , in a controlled release formulation, in a liposomal form, in a lyophilized form or in a unit dosage form.
16. A fusion polypeptide comprising the peptide of claim 1 further comprising a polypeptide of interest linked to the peptide.
17. The fusion polypeptide of claim 16 , wherein the polypeptide of interest comprises an immunogenic molecule.
18. The fusion peptide of claim 16 , wherein the peptide and the polypeptide of interest are separated by a peptide linker.
19. A method of modulating inflammation, asthma, allergy, cell proliferative disorders, metastasis of cancer cells, ion transport disorders, magnesium transport defects in the kidney, inflammatory bowel disease, Clostridium perfringens enterotoxin (CPE) infection, myelin sheath formation disorder, multiple sclerosis (MS), autoimmune encephalomyelitis, optic neuritis, and progressive multifocal leukoencephalopathy (PML), the method comprising administering to a subject the peptide of claim 1 or 13 , or a fusion polypeptide of claim 16 either alone or optionally with a pharmaceutically acceptable carrier.
20. A method of targeting a therapeutic to mucosal M cells comprising linking a therapeutic moiety to the peptide of claim 1 , 13 , or a fusion polypeptide of claim 16 and contacting a mucosal M cell with the peptide or fusion polypeptide.
21. The method of claim 20 , wherein the mucosal M cell is in vivo.
22. The method of claim 20 , wherein the therapeutic moiety is a cytotoxic drug, an immunopotentiating drug, an inhibitory nucleic acid molecule, a peptide, a polypeptide or a peptidomimetic.