IP Library Granted Patent US 7,528,227
Granted Patent B2
US 7,528,227 · App. 11/527,162 · Granted May 5, 2009

Histone H2A peptide derivatives and uses thereof

Assignee: Yissum Research Development Company of the Hebrew University of Jerusalem
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Quick Facts
Patent No.
US 7,528,227
App. No.
11/527,162
Granted
May 5, 2009
Kind
B2
Abstract

Peptides derived from a segment of human histone H2A, the segment corresponding to amino acid residues 36-44 of human histone H2A, are capable of reducing or ameliorating the extent of injury induced by noxious stimuli when administered to animals. Pharmaceutical compositions and methods of using these peptides are also disclosed. The pharmaceutical compositions according to the invention are useful for treating and protecting against inflammatory diseases, autoimmune diseases, for treating and protecting against tissue damage, for inhibiting metalloproteinase activity, and for treating and protecting against diseases associated with the breakdown of extracellular matrix or connective tissues.

Claims (10)

1. A nine amino acid peptide consisting of the amino acid sequence as set forth in any one of SEQ ID NOS: 7-30 and in any one of SEQ ID NOS:32-42, wherein the peptide has at least one activity selected from the group consisting of anti-inflammatory activity, free radical scavenging activity, metal chelating activity, metalloproteinase inhibitory activity, and T cell inhibitory activity.

2. A peptide of five to eight amino acid residues consisting of the amino acid sequence as set forth in any one of SEQ ID NOS: 44-47, 49, 50, 52-54, 61-62, 64, and 65, wherein the peptide has at least one activity selected from the group consisting of anti-inflammatory activity, free radical scavenging activity, metal chelating activity, metalloproteinase inhibitory activity, and T cell inhibitory activity.

3. A peptide having ten to sixteen amino acid residues having an amino acid sequence as set forth in any one of SEQ ID NOS: 67-83, wherein the peptide has at least one activity selected from the group consisting of anti-inflammatory activity, free radical scavenging activity, metal chelating activity, metalloproteinase inhibitory activity, and T cell inhibitory activity.

4. A peptide having the amino acid sequence KGHYAERVGC set forth in SEQ ID NO:90 or a peptide derivative thereof, wherein the peptide derivative is selected from the group consisting of an N-acetylated peptide, C-amidated peptide, and an N-acetylated and C-amidated peptide, the peptide or peptide derivative has at least one activity selected from the group consisting of anti-inflammatory activity, free radical scavenging activity, metal chelating activity, metalloproteinase inhibitory activity, and T-cell inhibitory activity.

5. The peptide according to claim 4 having the amino acid sequence set forth in SEQ ID NO:90.

6. A pharmaceutical composition comprising as an active ingredient a peptide according to claim 1 and a pharmaceutically acceptable earner.

7. A pharmaceutical composition comprising as an active ingredient a peptide according to claim 4 and a pharmaceutically acceptable carrier.

8. The pharmaceutical composition according to claim 7 , wherein the peptide has the amino acid sequence as set forth in SEQ ID NO:90.

9. A pharmaceutical composition comprising as an active ingredient a peptide according to claim 2 and a pharmaceutically acceptable carrier.

10. A pharmaceutical composition comprising as an active ingredient a peptide according to claim 3 and a pharmaceutically acceptable carrier.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 10, 2007
From: WORMSER, URI
To: YISSUM RESEARCH DEVELOPMENT COMPANY OF THE HEBREW UNIVERSITY OF JERUSALEM
Reel/Frame 018736/0159 →
Continuity (4)
Continuation In Part PCTIL200500032800 · Mar 23, 2005
Provisional Application 6055533400 · Mar 23, 2004
Provisional Application 6083121600 · Jul 17, 2006
Related Publication 20070093426A1 · Apr 26, 2007