IP Library Granted Patent US 9,090,701
Granted Patent B2
US 9,090,701 · App. 13/605,341 · Granted Jul 28, 2015

Methods of detecting oxidized calcium/calmodulin dependent protein kinase II

Inventors: Mark E. Anderson (Iowa City, IA); Peter J. Mohler (Iowa City, IA); Douglas R. Spitz, Jr. (Iowa City, IA); Jeffrey Robert Erickson (Utrecht, NL)
Assignee: University of Iowa Research Foundation
C07K16/40C07K16/44G01N33/57484G01N2800/26G01N2800/2821G01N2800/32
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Quick Facts
Patent No.
US 9,090,701
App. No.
13/605,341
Granted
Jul 28, 2015
Kind
B2
Abstract

Calcium/calmodulin dependent protein kinase II (CaMKII) has been found to be directly oxidized, and direct oxidation of CaMKII was observed to result in calcium independent activation of CaMKII. Antibodies that bind specifically to oxidized forms of CaMKII (oxCaMKII) were generated and were utilized to detect oxCaMKII in blood from: (1) mice with cancer; (2) mice with a knock out of the gene encoding methionine sulfoxide reductase; (3) mice injected with angiotensin II; (4) mice injected with bacterial endotoxin; (5) mice fed a pro-oxidant (ketogenic) diet; and (6) mice with cancer that had been treated with experimental therapy.

Claims (9)

1. A method of detecting oxidized calcium/calmodulin-dependent protein kinase II (oxCaMKII), the method comprising: (a) contacting a biological sample from a patient with a composition comprising a purified monoclonal antibody or antigen-binding fragment thereof that binds specifically to oxCaMKII to form a complex, wherein the monoclonal antibody or antigen-binding fragment binds specifically to oxCaMKII delta having an amino acid sequence comprising SEQ ID NO:12 and having oxidized methionine residues at positions 281 and 282, and wherein the monoclonal antibody or antigen-binding fragment does not bind to CaMKII delta having an amino acid sequence comprising SEQ ID NO:12 and having non-oxidized methionine residues at positions 281 and 282; and (b) detecting the complex.

2. The method of claim 1 , wherein the biological sample is blood or plasma.

3. The method of claim 1 , further comprising: (c) characterizing cardiac disease in the patient.

4. The method of claim 1 , wherein the patient has or is at risk for developing a disease or condition selected from a group consisting of cardiac disease, cancer, premature aging, atherosclerosis, Alzheimer's disease, or sepsis, and the method further comprises: (c) administering a therapeutic agent based on detecting or not detecting oxCaMKII.

5. The method of claim 1 , wherein the patient is undergoing therapy with an angiotensin converting enzyme (ACE) inhibitor and the method further comprises: (c) modulating the therapy based on detecting or not detecting oxCaMKII.

6. The method of claim 1 , wherein modulating the therapy comprises increasing dosage of the ACE inhibitor.

7. The method of claim 6 , wherein modulating the therapy comprises decreasing dosage of the ACE inhibitor or ceasing the therapy.

8. The method of claim 1 , wherein the patient is undergoing anti-cancer therapy and the method further comprises: (c) modulating the therapy based on detecting or not detecting oxCaMKII.

9. The method of claim 8 , wherein the anti-cancer therapy is selected from a group consisting of radiation therapy, chemotherapy, nutritional therapy, and combinations thereof.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 14, 2013
From: ANDERSON, MARK E.; MOHLER, PETER J.; SPITZ, DOUGLAS R., JR.; ERICKSON, JEFFREY ROBERT
To: UNIVERSITY OF IOWA RESEARCH FOUNDATION
Reel/Frame 029624/0233 →
CONFIRMATORY LICENSE Recorded Oct 23, 2012
From: UNIVERSITY OF IOWA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 029177/0280 →
Continuity (3)
Division 12430644 · Apr 27, 2009
Provisional Application 61048259 · Apr 28, 2008
Related Publication 20130012568A1 · Jan 10, 2013