IP Library Granted Patent US 9,493,508
Granted Patent B2
US 9,493,508 · App. 13/934,933 · Granted Nov 15, 2016

Polypeptide inhibitors of HSP27 kinase and uses therefor

Inventors: Alyssa Panitch (West Lafayette, IN); Brandon Seal (Pleasant Grove, UT); Brian C. Ward (Brownsburg, IN)
Assignee: Purdue Research Foundation
C07K7/06C07K7/08C07K14/001A61K38/00
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,493,508
App. No.
13/934,933
Granted
Nov 15, 2016
Kind
B2
Abstract

The present invention provides polypeptide inhibitors of HSP27 kinase, compositions thereof, and methods for using such polypeptides and compositions for various therapeutic uses.

Claims (11)

1. A method for treating a disease, disorder or a condition in a subject in need thereof characterized by inhibiting excretion of TNF-α from monocytes selected from the group consisting of osteoarthritis, rheumatoid arthritis, gliosis, and scar formation in the central nervous system, the method comprising the step of:

administering a therapeutic amount of a composition comprising an isolated polypeptide and a pharmaceutically acceptable carrier;

wherein the polypeptide comprises a sequence Z1-X1-X2-X3-X4-X5-X6-X7-X8-X9-X10-Z2 (Formula I) (SEQ ID NO: 69);

wherein Z1 and Z2 are independently absent or are transduction domains; and

wherein X1-X2-X3-X4-X5-X6-X7-X8-X9-X10 is an amino acid sequence selected from the group consisting of the amino acid sequence KALARQLGVAA (SEQ ID NO: 62), the amino acid sequence KALNRQLAVAA (SEQ ID NO: 66), and the amino acid sequence KALNRQLGVA (SEQ ID NO: 68).

2. The method according to claim 1 , further comprising the steps of

monitoring a level of at least one biomarker in a target tissue, wherein the at least one biomarker is selected from the group consisting of: TGF01 expression; collagen I expression; CTGF expression; a-smooth muscle actin expression; TNF-α; IL-1; IL-6; IL-8; COX-2; MIP-1α; and MIP-2; and

maintaining the level of the biomarker in the target tissue substantially at normal levels during treatment.

3. The method of claim 1 , wherein the polypeptide is KAFAKLAARLYRKALARQLGVAA (SEQ ID NO: 48).

4. The method of claim 1 , wherein the polypeptide is FAKLAARLYRKALARQLGVAA (SEQ ID NO: 49).

5. The method of claim 1 , wherein the polypeptide is YARAAARQARAKALNRQLGVA (SEQ ID NO. 55).

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 22, 2015
From: PANITCH, ALYSSA; SEAL, BRANDON; WARD, BRIAN
To: PURDUE RESEARCH FOUNDATION
Reel/Frame 037351/0565 →
CONFIRMATORY LICENSE Recorded Sep 27, 2013
From: PURDUE UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 031301/0845 →
Continuity (3)
Division 11972459 · Jan 10, 2008
Provisional Application 60880137 · Jan 10, 2007
Related Publication 20140112947A1 · Apr 24, 2014