IP Library Granted Patent US 8,822,636
Granted Patent B2
US 8,822,636 · App. 12/956,900 · Granted Sep 2, 2014

Peptides for activation and inhibition of δPKC

Inventors: Daria Mochly-Rosen (Menlo Park, CA); Leon E. Chen (Belmont, CA)
Assignee: The Board of Trustees of The Leland Stanford Junior University
C12N9/12C07K5/101A61K38/00
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Quick Facts
Patent No.
US 8,822,636
App. No.
12/956,900
Granted
Sep 2, 2014
Kind
B2
Abstract

Peptides able to inhibit or activate the translocation or function of δPKC are identified. Administration of the peptides for protection or enhancement of cell damage due to ischemia is described. Therapeutic methods to reduce damage to cells or to enhance damage to cells due to ischemia are also described, as well as methods for screening test compounds for δPKC-selective agonists and antagonists.

Claims (18)

1. A composition comprising a synthetic peptide consisting of δV1-2 (SEQ ID NO:5) linked to a moiety effective to facilitate transport across a cell membrane, wherein the synthetic peptide is at least 95% of the composition.

2. The composition of claim 1 , wherein the moiety is selected from the group consisting of a Tat-derived peptide, an Antennapedia carrier peptide, and a polyarginine peptide.

3. The composition of claim 1 , wherein the peptide and the moiety are linked to form a fusion peptide.

4. The composition of claim 3 , wherein the moiety is selected from the group consisting of a Tat-derived peptide, an Antennapedia carrier peptide, and a polyarginine peptide.

5. The composition of claim 3 , wherein the moiety comprises an amino acid sequence selected from the group consisting of SEQ ID NO:8 and SEQ ID NO:9.

6. The composition of claim 3 , wherein the moiety consists of an amino acid sequence selected from the group consisting of SEQ ID NO:8 and SEQ ID NO:9.

7. The composition of claim 3 , wherein the moiety comprises the amino acid sequence of SEQ ID NO:9.

8. The composition of claim 3 , wherein the moiety consists of the amino acid sequence of SEQ ID NO:9.

9. The composition of claim 1 , wherein the peptide and the moiety are linked by a Cys-Cys bond.

10. The composition of claim 9 , wherein the moiety is selected from the group consisting of a Tat-derived peptide, an Antennapedia carrier peptide, and a polyarginine peptide.

11. The composition of claim 9 , wherein the moiety comprises an amino acid sequence selected from the group consisting of SEQ ID NO:8 and SEQ ID NO:9.

12. The composition of claim 9 , wherein the moiety consists of an amino acid sequence selected from the group consisting of SEQ ID NO:8 and SEQ ID NO:9.

13. The composition of claim 9 , wherein the moiety comprises the amino acid sequence of SEQ ID NO:9.

14. The composition of claim 9 , wherein the moiety consists of the amino acid sequence of SEQ ID NO:9.

15. A conjugate comprising:

a first peptide consisting of δV1-2 (SEQ ID NO:5) and a terminal cysteine, and

a second peptide consisting of the amino acid sequence of SEQ ID NO:9,

wherein the first and second peptides are linked by a Cys-Cys bond.

Assignments (1)
CONFIRMATORY LICENSE Recorded Mar 4, 2011
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 025898/0874 →
Continuity (5)
Division 11838732 · Aug 14, 2007
Continuation 10843731 · May 12, 2004
Division 10007761 · Nov 9, 2001
Provisional Application 60262060 · Jan 18, 2001
Related Publication 20110143991A1 · Jun 16, 2011