IP Library Granted Patent US 7,923,219
Granted Patent B2
US 7,923,219 · App. 11/915,610 · Granted Apr 12, 2011

Ubiquitin E3 ligase

Assignee: The University of North Carolina at Chapel Hill
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Quick Facts
Patent No.
US 7,923,219
App. No.
11/915,610
Granted
Apr 12, 2011
Kind
B2
Abstract

The present invention provides a native or reconstituted complex comprising Bmi1 and/or Ring1 and/or Ring2, wherein the complex has ubiquitin E3 ligase activity. Optionally, the complex further comprises HPH2 and/or HPC3. Also disclosed are methods of producing the reconstituted complex, methods of identifying compounds that modulate the ubiquitin E3 ligase activity of the native or reconstituted complex, and methods of identifying candidate compounds for treating cancer. Kits for determining modulation of protein ubiquitination and/or for ubiquitinating a target substrate are further provided.

Claims (25)

1. A method of identifying a compound that modulates ubiquitin E3 ligase activity of Ring2, the method comprising:

contacting Ring2 with a protein substrate in the presence of a test compound; and

detecting the level of ubiquitination of the protein substrate under conditions sufficient to provide ubiquitination of the protein substrate, wherein a change in ubiquitination of the protein substrate as compared with the level of ubiquitination of the protein substrate in the absence of the test compound indicates that the test compound is a modulator of the ubiquitin E3 ligase activity of Ring2.

2. The method of claim 1 , wherein the method is a method of identifying a compound that modulates histone ubiquitin E3 ligase activity of Ring2.

3. The method of claim 2 , wherein the method is a method of identifying a compound that modulates histone H2A ubiquitin E3 ligase activity of Ring2.

4. The method of claim 3 , wherein the method is a method of identifying a compound that modulates histone H2A-K119 ubiquitin E3 ligase activity of Ring2.

5. The method of claim 2 , wherein the histone substrate is a core histone, a mononucleosome, a dinucleosome or an oligonucleosome.

6. The method of claim 1 , wherein the Ring2 is a recombinant protein.

7. The method of claim 1 , wherein a reduction in ubiquitination of the protein substrate as compared with the level of ubiquitination of the protein substrate in the absence of the test compound indicates that the test compound is an inhibitor of the ubiquitin E3 ligase activity of Ring2.

8. The method of claim 1 , wherein an increase in ubiquitination of the protein substrate as compared with the level of ubiquitination of the protein substrate in the absence of the test compound indicates that the test compound is an activator of the ubiquitin E3 ligase activity of Ring2.

9. The method of claim 1 , wherein the method is a cell-free method.

10. A method of identifying a compound that modulates ubiquitin E3 ligase activity of a complex comprising Ring2, the method comprising:

contacting the complex with a protein substrate in the presence of a test compound; and

detecting the level of ubiquitination of the protein substrate under conditions sufficient to provide ubiquitination of the protein substrate, wherein a change in ubiquitination of the protein substrate as compared with the level of ubiquitination of the protein substrate in the absence of the test compound indicates that the test compound is a modulator of the ubiquitin E3 ligase activity of the complex.

11. The method of claim 10 , wherein the complex comprises Ring2, Ring1, Bmi1 and HPH2.

12. The method of claim 10 , wherein the complex comprises dRing1, Psc and ph.

13. The method of claim 10 , wherein the method is a method of identifying a compound that modulates histone ubiquitin E3 ligase activity of the complex.

14. The method of claim 13 , wherein the method is a method of identifying a compound that modulates histone H2A ubiquitin E3 ligase activity of the complex.

15. The method of claim 14 , wherein the method comprises detecting the level of H2A-K119 ubiquitination.

16. The method of claim 10 , wherein the complex is a recombinant complex.

17. The method of claim 10 , wherein a reduction in ubiquitination of the protein substrate as compared with the level of ubiquitination of the protein substrate in the absence of the test compound indicates that the test compound is an inhibitor of the ubiquitin E3 ligase activity of the complex.

18. The method of claim 10 , wherein an increase in ubiquitination of the protein substrate as compared with the level of ubiquitination of the protein substrate in the absence of the test compound indicates that the test compound is an activator of the ubiquitin E3 ligase activity of the complex.

19. A method of identifying a candidate compound for treating cancer, the method comprising:

contacting Ring2 with a histone H2A substrate in the presence of a test compound; and

detecting the level of ubiquitination of the histone H2A substrate under conditions sufficient to provide histone H2A ubiquitination, wherein a reduction in histone H2A ubiquitination as compared with the level of histone H2A ubiquitination in the absence of the test compound indicates that the test compound is a candidate compound for the treatment of cancer.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jan 30, 2018
From: UNIV OF NORTH CAROLINA CHAPEL HILL
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 045186/0138 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 21, 2008
From: CAO, RU; WANG, HENGBIN; ZHANG, YI
To: THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL
Reel/Frame 020977/0339 →
Continuity (3)
Provisional Application 60686769 · Jun 2, 2005
Provisional Application 60750564 · Dec 15, 2005
Related Publication 20080248458A1 · Oct 9, 2008