IP Library Granted Patent US 7,374,895
Granted Patent B2
US 7,374,895 · App. 11/447,407 · Granted May 20, 2008

Guanosine triphosphate (GTP) binding protein-coupled receptor proteins that bind histamine and are expressed in the brain

Assignee: Banyu Pharmaceutical Co., Ltd.
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Quick Facts
Patent No.
US 7,374,895
App. No.
11/447,407
Granted
May 20, 2008
Kind
B2
Abstract

A full-length cDNA encoding a human-derived G protein-coupled receptor protein is isolated by screening a human hippocampus library. Also, a rat-derived cDNA corresponding to the human-derived cDNA is isolated. Proteins encoded by these cDNAs have an activity of lowering intracellular cAMP concentration under stimulation with histamine. These proteins are usable as tools in screening ligands thereof or in screening candidate compounds for drugs capable of regulating signal transduction from the above proteins.

Claims (22)

1. A method for identifying a compound that modulates a histamine binding activity, the method comprising:

a) contacting (i) a polypeptide or (ii) a cell transfected with a nucleic acid encoding the polypeptide with a test compound, wherein the polypeptide comprises an amino acid sequence at least 95% identical to SEQ ID NO:20 or 25 and has a histamine binding activity; and

b) determining whether the test compound modulates the histamine binding activity of the polypeptide or cell,

thereby identifying a compound that modulates a histamine binding activity.

2. The method of claim 1 , wherein the method further comprises determining whether the test compound modulates cellular cAMP concentration, cellular calcium concentration, a G protein activation, phospholipase C activation, or intracellular pH.

3. The method of claim 1 , wherein the polypeptide comprises an amino acid sequence of a naturally occurring protein which binds to histamine.

4. The method of claim 1 , wherein the polypeptide comprises the amino acid sequence of SEQ ID NO:20.

5. The method of claim 1 , wherein the polypeptide comprises the amino acid sequence of SEQ ID NO:25.

6. The method of claim 1 , wherein step a) comprises contacting the polypeptide with the test compound.

7. The method of claim 6 , wherein the polypeptide comprises an amino acid sequence of a naturally occurring protein which binds to histamine.

8. The method of claim 6 , wherein the polypeptide comprises the amino acid sequence of SEQ ID NO:20.

9. The method of claim 6 , wherein the polypeptide comprises the amino acid sequence of SEQ ID NO:25.

10. The method of claim 1 , wherein step a) comprises contacting the cell of (ii) with the test compound.

11. The method of claim 10 , wherein the polypeptide comprises an amino acid sequence of a naturally occurring protein which binds to histamine.

12. The method of claim 10 , wherein the polypeptide comprises the amino acid sequence of SEQ ID NO:20.

13. The method of claim 10 , wherein the polypeptide comprises the amino acid sequence of SEQ ID NO:25.

14. A method for identifying a compound that modulates a histamine binding activity, the method comprising:

a) contacting (i) a polypeptide or (ii) a cell transfected with a nucleic acid encoding the polypeptide with a test compound, wherein the polypeptide has a histamine binding activity and is encoded by a polynucleotide which hybridizes to a polynucleotide consisting of a complementary sequence of SEQ ID NO:21 or 26 under the conditions of 6×SSC, 40% formamide at 37° C., followed by a wash in 0.1×SSC containing 0.1% SDS at 62° C.; and

b) determining whether the test compound modulates the histamine binding activity of the polypeptide or cell,

thereby identifying a compound that modulates a histamine binding activity.

15. The method of claim 14 , wherein the method further comprises determining whether the test compound modulates cellular cAMP concentration, cellular calcium concentration, a G protein activation, phospholipase C activation, or intracellular pH.

16. The method of claim 14 , wherein the polypeptide comprises an amino acid sequence of a naturally occurring protein which binds to histamine.

Assignments (3)
RELEASE OF SECURITY INTEREST Recorded Sep 5, 2025
From: AVENUE VENTURE OPPORTUNITIES FUND, L.P.
To: SOURCE GLOBAL, PBC
Reel/Frame 072814/0093 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 9, 2011
From: BANYU PHARMACEUTICAL CO., LTD.
To: MSD K.K.
Reel/Frame 025920/0079 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 1, 2006
From: ITADANI, HIRAKU; TAKIMURA, TETSUO; NAKAMURA, TAKAO; KOBAYASHI, MASAHIKO; TANAKA, KEN-ICHI; HIDAKA, YUSUKE; OHTA, MASATAKA
To: BANYU PHARMACEUTICAL CO., LTD.
Reel/Frame 018045/0964 →
Priority Claims (2)
WO PCT/JP98/05967 · Dec 25, 1998 · international
JP 11/145661 · May 25, 1999 · national
Continuity (4)
Division 1075946300 · Jan 16, 2004
Division 0989105300 · Jun 25, 2001
Continuation In Part PCTJP990728000 · Dec 24, 1999
Related Publication 20070015220A1 · Jan 18, 2007