IP Library Granted Patent US 7,868,150
Granted Patent B2
US 7,868,150 · App. 12/544,854 · Granted Jan 11, 2011

Nucleic acids encoding T2R taste receptors

Assignee: The Regents of the University of California
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Quick Facts
Patent No.
US 7,868,150
App. No.
12/544,854
Granted
Jan 11, 2011
Kind
B2
Abstract

The invention provides nucleic acid and amino acid sequences for a novel family of taste transduction G-protein coupled receptors, antibodies to such receptors, methods of detecting such nucleic acids and receptors, and methods of screening for modulators of taste transduction G-protein coupled receptors.

Claims (20)

1. An isolated nucleic acid encoding a taste transduction G protein-coupled receptor having G protein-coupled receptor activity, the receptor comprising a polypeptide with greater than 90% amino acid sequence identity to SEQ ID NO:15, wherein said receptor detects bitter tastants.

2. The nucleic acid of claim 1 , wherein the polypeptide sequence is SEQ ID NO:15.

3. The nucleic acid of claim 1 , wherein the polypeptide has greater than 95% amino acid sequence identity to SEQ ID NO:15.

4. An isolated expression vector comprising the nucleic acid of claim 1 .

5. An isolated cell comprising the expression vector of claim 4 .

6. A method for identifying a compound that modulates taste signaling in taste cells, the method comprising the steps of:

(i) contacting the taste transduction G protein-coupled receptor polypeptide encoded by the nucleic acid of claim 1 in a cell with the compound; and

(ii) determining the functional effect of the compound upon the polypeptide, thereby identifying a compound that modulates taste signaling in taste cells.

7. The method of claim 6 , wherein the functional effect is determined by measuring binding of the compound to an extracellular domain or a transmembrane region of the polypeptide.

8. The method of claim 6 , wherein the functional effect is determined by measuring binding of radiolabeled GTP to the polypeptide.

9. The method of claim 6 , wherein the polypeptide is recombinant.

10. The method of claim 6 , wherein the functional effect is measured by determining changes in the electrical activity in the cell expressing the polypeptide.

11. The method of claim 6 , wherein the functional effect is determined by measuring changes in intracellular cAMP, cGMP, IP3, or Ca 2+ .

12. The method of claim 6 , wherein the cell is an HEK-293 cell.

13. The method of claim 6 , wherein the polypeptide is a fusion protein comprising at least about 20 consecutive N-terminal amino acids of a rhodopsin protein.

14. The method of claim 6 , wherein the cell comprises Gα15.

15. The method of claim 6 , wherein the polypeptide is contacted with the compound in the presence of a bitter tastant, and wherein a difference in the functional effect of the bitter tastant on the cell in the presence of the compound and the functional effect of the bitter tastant on the cell in the absence of the compound indicates that the compound is capable of modulating taste signaling in taste cells.

16. The method of claim 6 , wherein the polypeptide is covalently linked to a heterologous polypeptide, forming a chimeric polypeptide.

17. The method of claim 6 , wherein the polypeptide is linked to a solid phase.

18. The method of claim 6 , wherein said polypeptide comprises a sequence with at least 95% identity to SEQ ID NO:15.

Assignments (1)
CONFIRMATORY LICENSE Recorded Jan 11, 2011
From: UNIVERSITY OF CALIFORNIA SAN DIEGO
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 025615/0684 →
Continuity (5)
Division 1197808800 · Oct 25, 2007
Continuation 1098236500 · Nov 5, 2004
Continuation 0951033200 · Feb 22, 2000
Continuation In Part 0939363400 · Sep 10, 1999
Related Publication 20100062456A1 · Mar 11, 2010