IP Library Granted Patent US 9,365,837
Granted Patent B2
US 9,365,837 · App. 14/187,070 · Granted Jun 14, 2016

Peptide inhibitors of protein kinase C

Inventor: Daria Mochly-Rosen (Menlo Park, CA)
Assignee: The Board of Trustees of the Leland Stanford Junior University
C12N9/1205A61K38/45C07K7/06C07K7/08
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Quick Facts
Patent No.
US 9,365,837
App. No.
14/187,070
Granted
Jun 14, 2016
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 (17)

1. A method for protecting cardiac tissue from damage due to an ischemic or hypoxic event comprising:

administering to a mammal in need thereof, a therapeutically effective amount of a peptide consisting of a contiguous sequence of six to twelve amino acid residues that is at least 80% identical to a contiguous sequence of six to twelve amino acid residues of a variable 5 (V5) domain of a delta protein kinase C (PKC) isozyme (SEQ ID NO:26), wherein the peptide is linked to a carrier peptide, and wherein the peptide inhibits delta PKC isozyme activity.

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

3. The method of claim 1 , wherein the peptide is six to eight amino acids in length.

4. The method of claim 1 , wherein the peptide is a sequence selected from the group consisting of SEQ ID NO:27, SEQ ID NO:28, SEQ ID NO:29 and SEQ ID NO:30.

5. The method of claim 1 , wherein the carrier peptide is selected from the group consisting of poly-Arg, a Tat-derived peptide, and Drosophilla Antennapedia homeodomain.

6. The method of claim 1 , wherein the carrier peptide is a Tat-derived peptide.

7. The method of claim 1 , wherein the carrier peptide is SEQ ID NO:65.

8. The method of claim 1 , wherein the peptide is linked to the carrier peptide by a Cys-Cys linkage.

9. A method for treating cardiac hypertrophy and heart failure comprising:

administering to a mammal in need thereof, a therapeutically effective amount of a peptide consisting of a contiguous sequence of six to twelve amino acid residues that is at least 80% identical to a contiguous sequence of six to twelve amino acid residues of a variable 5 (V5) domain of a β II protein kinase C (PKC) isozyme (SEQ ID NO:14), wherein the peptide inhibits β II PKC isozyme activity, wherein the peptide is linked to a carrier peptide.

10. The method of claim 9 , wherein the peptide is six to eight amino acids in length.

11. The method of claim 9 , wherein the peptide is a sequence selected from the group consisting of SEQ ID NO:15, SEQ ID NO:16, SEQ ID NO:17 and SEQ ID NO:18.

12. The method of claim 9 , wherein the carrier peptide is selected from the group consisting of poly-Arg, a Tat-derived peptide, and Drosophilla Antennapedia homeodomain.

13. The method of claim 9 , wherein the carrier peptide is a Tat-derived peptide.

14. The method of claim 9 , wherein the carrier peptide is SEQ ID NO:65.

15. The method of claim 9 , wherein the peptide is linked to the carrier peptide by a Cys-Cys linkage.

Assignments (1)
CONFIRMATORY LICENSE Recorded May 1, 2014
From: THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 032796/0816 →
Continuity (5)
Division 13101540 · May 5, 2011
Continuation 12214104 · Jun 16, 2008
Continuation 10513003
Provisional Application 60374530 · Apr 22, 2002
Related Publication 20140178352A1 · Jun 26, 2014