IP Library Granted Patent US 8,859,232
Granted Patent B2
US 8,859,232 · App. 13/381,383 · Granted Oct 14, 2014

Genetically encoded photomanipulation of protein and peptide activity

Inventors: Klaus Hahn (Chapel Hill, NC); Yi Wu (Farmington, CT); Brian Kuhlman (Chapel Hill, NC)
Assignee: The University of North Carolina at Chapel Hill
G01N33/542C07K2319/73C12N9/16
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Quick Facts
Patent No.
US 8,859,232
App. No.
13/381,383
Granted
Oct 14, 2014
Kind
B2
Abstract

The present invention relates to fusion proteins comprising protein light switches and methods of photomanipulating the activity of the proteins. The invention further relates to polynucleotides and vectors encoding the fusion proteins, cells comprising the fusion proteins, and methods of using the fusion proteins to study protein function and analyze subcellular activity, as well as diagnostic and therapeutic methods.

Claims (19)

1. A fusion protein comprising a protein of interest fused to a protein light switch comprising a light, oxygen or voltage (LOV) domain, wherein illumination of the fusion protein activates or inactivates the protein of interest, and wherein the protein of interest and the protein light switch are not found fused together in nature.

2. The fusion protein of claim 1 , wherein the activation or inactivation is reversible.

3. The fusion protein of claim 1 , wherein the activation or inactivation is dose dependent.

4. The fusion protein of claim 1 , wherein illumination activates the protein of interest.

5. The fusion protein of claim 1 , wherein illumination inactivates the protein of interest.

6. The fusion protein of claim 1 , wherein the illumination is with visible light.

7. The fusion protein of claim 1 , wherein the protein light switch comprises a LOV2 domain.

8. The fusion protein of claim 1 , wherein the protein light switch further comprises a Jα domain.

9. The fusion protein of claim 8 , wherein the protein of interest is fused in the Jα domain.

10. The fusion protein of claim 1 , wherein the protein light switch comprises a fragment of a phototropin.

11. The fusion protein of claim 10 , wherein the phototropin is an Avena sativa (oat) phototropin 1.

12. The fusion protein of claim 1 , wherein the protein light switch comprises a fragment of an aureochrome.

13. The fusion protein of claim 12 , wherein the fragment of an aureochrome comprises a LOV domain and a coiled-coil domain.

14. The fusion protein of claim 1 , wherein the fusion protein further comprises a linker between the protein of interest and the protein light switch.

15. A method of activating or inactivating a protein of interest present in the fusion protein of claim 1 , comprising illuminating the fusion protein.

16. The fusion protein of claim 1 , wherein the protein of interest is a mammalian protein.

17. The fusion protein of claim 1 , wherein the protein of interest is a human protein.

18. The fusion protein of claim 1 , wherein the protein of interest is a first member of a protein binding pair comprising a first member and a second member, wherein binding of the first member to the second member is modulated by illumination.

19. The fusion protein of claim 1 , wherein the protein of interest is a functional domain of a protein.

Assignments (2)
CONFIRMATORY LICENSE Recorded Dec 12, 2012
From: THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 029457/0201 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 22, 2012
From: HAHN, KLAUS; WU, YI; KUHLMAN, BRIAN
To: THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL
Reel/Frame 027742/0952 →
Continuity (2)
Provisional Application 61222204 · Jul 1, 2009
Related Publication 20120165204A1 · Jun 28, 2012