IP Library Granted Patent US 10,300,107
Granted Patent B2
US 10,300,107 · App. 15/704,902 · Granted May 28, 2019

Compositions and methods for CaMKII inhibitors and uses thereof

Inventors: K. Ulrich Bayer (Denver, CO); Steve Coultrap (Denver, CO)
Assignee: THE REGENTS OF THE UNIVERSITY OF COLORADO, A BODY CORPORATE
A61K38/10A61K38/45A61K38/55A61K45/06C12N9/1205
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Quick Facts
Patent No.
US 10,300,107
App. No.
15/704,902
Granted
May 28, 2019
Kind
B2
Abstract

Embodiments herein generally relate to methods, compositions and uses of CaMKII inhibitors. Other embodiments relate to methods, compositions and uses of agents that target CaMKII. Yet further embodiments relate to compositions, methods and uses of CaMKIIN-derived molecules and other CaMKII inhibitor molecules that inhibit autonomous CaMKII activity. In accordance with these embodiments, compositions that inhibit autonomous CaMKII activity may be used for treating conditions causing neuronal cell death, for treating cancer or for treating neurodegenerative disorders.

Claims (15)

1. A method of reducing or eliminating CaMKII activity in a cell, the method comprising: exposing the cell to a purified polypeptide comprising an amino acid sequence of:

SEQ ID NO:23 or amino acid substitutions thereof, wherein the purified polypeptide is a derivative of CaMKIIN, and wherein the amino acid substitutions of SEQ ID NO:23 comprise the following amino acid substitutions:

amino acid at position three of SEQ ID NO: 23 is proline, arginine, or lysine;

amino acid at position twelve of SEQ ID NO: 23 is serine or arginine; and

amino acid at position thirteen of SEQ ID NO: 23 is alanine; or

SEQ ID NO:24 or an amino acid substitution thereof; wherein the purified polypeptide is a derivative of CaMKIIN, and wherein SEQ ID NO:24 consists of a phenylalanine at amino acid position fifteen of SEQ ID NO:24; and

wherein exposing the cell to the purified polypeptide reduces or eliminates CaMKII activity in the cell.

2. The method of claim 1 , further comprising a cell-transfer/penetrating agent associated with the purified polypeptide.

3. The method of claim 1 , wherein the cell is a neuronal cell and reducing or eliminating CaMKII activity in the neuronal cell prolongs survival of the neuronal cell.

4. The method of claim 2 , wherein the cell-transfer/penetrating agent comprises tat, ant, meristyl-group, palmityl-group or combination thereof.

5. The method of claim 1 , wherein the purified polypeptide is the amino acid sequence represented by SEQ ID NO:23 or SEQ ID NO:24.

6. The method of claim 1 , wherein the purified polypeptide further comprises a cell-transfer/penetrating agent.

7. The method of claim 6 , wherein the cell-transfer/penetrating agent comprises tat, ant, or a combination thereof.

8. The method of claim 6 , wherein the cell-transfer/penetrating agent is tat and the purified polypeptide is tatCN19a2v (tat-SEQ ID NO:23) or tatCN19o (tat-SEQ ID NO:24).

9. The method of claim 1 , wherein exposing the cell comprises treating a subject with a pharmaceutical composition comprising the purified polypeptide or a pharmaceutically acceptable derivative or salt thereof; and wherein treating the subject with the pharmaceutical composition reduces neuronal cell death in the subject.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 14, 2017
From: BAYER, K. ULRICH; COULTRAP, STEVE
To: THE REGENTS OF THE UNIVERSITY OF COLORADO, A BODY CORPORATE
Reel/Frame 043594/0841 →
Continuity (7)
Continuation 14857646 · Sep 17, 2015
Continuation 14173751 · Feb 5, 2014
Continuation 13181373 · Jul 12, 2011
Continuation In Part 12679459
Provisional Application 60980766 · Oct 17, 2007
Provisional Application 60975329 · Sep 26, 2007
Related Publication 20170368136A1 · Dec 28, 2017