IP Library Granted Patent US 7,833,984
Granted Patent B2
US 7,833,984 · App. 11/879,414 · Granted Nov 16, 2010

Peptide inhibitors of protein kinase C

Assignee: The Board of Trustees of the Leland Stanford Junior University
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Quick Facts
Patent No.
US 7,833,984
App. No.
11/879,414
Granted
Nov 16, 2010
Kind
B2
Abstract

PKC V5 isozyme-specific peptides are described. The sequences and compositions comprising the sequences are useful for treating disease states associated with the PKC isozyme from which they are respectively derived. Methods of treatment, pharmaceutical formulations and methods of identifying compounds that mimic the activity of the peptides are also described.

Claims (30)

1. A peptide consisting of a contiguous sequence of six to twelve amino acid residues selected from the N-terminal 15 amino acid residues of the variable 5 (V5) domain of the delta protein kinase C (PKC) isozyme (SEQ ID NO:26).

2. The peptide of claim 1 , wherein said peptide does not include the N-terminal 2 amino acid residues of said V5 domain.

3. The peptide of claim 1 , wherein said peptide is six to eight amino acid residues in length.

4. The peptide of claim 1 , wherein said peptide is linked to a carrier peptide selected from poly-Arg, a Tat-derived peptide, or the Drosophila Antennapedia homeodomain.

5. The peptide of claim 1 , wherein said peptide is a sequence selected from the group consisting of SEQ ID NO:27 and SEQ ID NO:28.

6. A pharmaceutical formulation comprising a pharmaceutically acceptable excipient and a peptide consisting of a contiguous sequence of six to twelve amino acid residues that is identical to a contiguous sequence of six to twelve amino acid residues selected from the N-terminal 15 amino acid residues of the variable 5 (V5) domain of the delta protein kinase C (PKC) isozyme (SEQ ID NO:26).

7. The pharmaceutical formulation of claim 6 , wherein said peptide does not include the N-terminal 2 amino acid residues of said the V5 domain.

8. The pharmaceutical formulation of claim 6 , wherein said peptide is six to eight amino acid residues in length.

9. The pharmaceutical formulation of claim 6 , wherein said peptide is linked to a carrier peptide selected from poly-Arg, a Tat-derived peptide, or the Drosophila Antennapedia homeodomain.

10. The pharmaceutical formulation of claim 6 , wherein said peptide is a sequence selected from the group consisting of SEQ ID NO:27 and SEQ ID NO:28.

11. The peptide of claim 4 , wherein said carrier peptide is SEQ ID NO:65.

12. The peptide of claim 5 , wherein said peptide is linked to a carrier peptide selected from the group consisting of poly-Arg, a Tat-derived peptide and the Drosophila Antennapedia homeodomain.

13. The peptide of claim 12 , wherein said carrier peptide is SEQ ID NO:65.

14. A peptide consisting of a sequence selected from the group consisting of SEQ ID NO:29 and SEQ ID NO:30.

15. The peptide of claim 14 , wherein said peptide is linked to a carrier peptide selected from the group consisting of poly-Arg, a Tat-derived peptide and the Drosophila Antennapedia homeodomain.

16. The peptide of claim 15 , wherein said carrier peptide is SEQ ID NO:65.

17. A pharmaceutical formulation comprising a pharmaceutically acceptable excipient and a peptide consisting of a sequence selected from the group consisting of SEQ ID NO:29 and SEQ ID NO:30.

18. The pharmaceutical formulation of claim 17 , wherein said peptide is linked to a carrier peptide selected from the group consisting of poly-Arg, a Tat-derived peptide and the Drosophila Antennapedia homeodomain.

19. The pharmaceutical formulation of claim 18 , wherein the said carrier peptide is SEQ ID NO:65.

20. A conjugate, comprising:

a peptide consisting of a contiguous sequence of six to twelve amino acid residues that is identical to a contiguous sequence of six to twelve amino acid residues selected from the N-terminal 15 amino acid residues of the variable 5 (V5) domain of the delta protein kinase C (PKC) isozyme (SEQ ID NO:26); and

a carrier peptide linked to said peptide, said carrier peptide selected from the group consisting of poly-Arg, a Tat-derived peptide and the Drosophila Antennapedia homeodomain.

21. The conjugate of claim 20 , wherein said peptide is linked to said carrier peptide by a Cys-Cys linkage.

22. The conjugate of claim 20 , wherein said peptide does not include the N-terminal 2 amino acid residues of said V5 domain.

23. The conjugate of claim 20 , wherein said peptide is six to eight amino acid residues in length.

24. The conjugate of claim 20 , wherein said peptide is a sequence selected from the group consisting of SEQ ID NO:27 and SEQ ID NO:28.

25. The conjugate of claim 20 , wherein said carrier peptide is SEQ ID NO:65.

26. A pharmaceutical formulation, comprising the conjugate of claim 20 .

27. The pharmaceutical formulation of claim 26 , wherein said peptide is linked to said carrier peptide by a Cys-Cys linkage.

28. The pharmaceutical formulation of claim 27 , wherein said carrier peptide is SEQ ID NO:65.

Assignments (1)
CONFIRMATORY LICENSE Recorded Aug 4, 2010
From: STANFORD UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 024786/0534 →
Continuity (4)
Continuation 1051300300
Continuation 1042150300 · Apr 22, 2003
Provisional Application 6037453000 · Apr 22, 2002
Related Publication 20080167247A1 · Jul 10, 2008