| US 7,547,523 B2 | ||
| Histamine receptor | ||
| Jiang X. Behan, Edison, N.J. (US); Joseph A. Hedrick, South River, N.J. (US); Thomas M. Laz, Parlin, N.J. (US); Frederick James Monsma, Jr., Summit, N.J. (US); Kelley L. Morse, Livingston, N.J. (US); Shelby P. Umland, Boonton Township, N.J. (US); and Suke Wang, Edison, N.J. (US) | ||
| Assigned to Schering Corporation, Kenilworth, N.J. (US) | ||
| Filed on Jan. 05, 2007, as Appl. No. 11/620,337. | ||
| Application 09/812216 is a division of application No. 09/414010, filed on Oct. 07, 1999, granted, now 6,204,017. | ||
| Application 11/620337 is a continuation of application No. 10/616088, filed on Jul. 08, 2003, granted, now 7,166,705. | ||
| Application 10/616088 is a continuation of application No. 09/812216, filed on Mar. 19, 2001, granted, now 6,613,533. | ||
| Prior Publication US 2007/0117155 A1, May 24, 2007 | ||
| This patent is subject to a terminal disclaimer. | ||
| Int. Cl. G01N 33/567 (2006.01); C07K 14/705 (2006.01) | ||
| U.S. Cl. 435—7.21 [435/7.2; 436/501] | 2 Claims |
| 1. A method for identifying an agonist or antagonist of a mammalian histamine receptor, comprising:
(a) contacting a polypeptide comprising the amino acid sequence defined by SEQ ID NO: 2 or a histamine binding fragment thereof
in the presence of a known amount of labeled histamine or a surrogate thereof with a sample to be tested for the presence
of a histamine agonist or antagonist;
(b) measuring the amount of labeled histamine or surrogate thereof specifically bound to the polypeptide;
(c) contacting cells expressing a polypeptide comprising the amino acid sequence defined by SEQ ID NO: 2 or a histamine binding
fragment thereof with said sample; and
(d) measuring at least one cellular function modulated by the binding of a ligand to a polypeptide comprising the amino acid
sequence defined by SEQ ID NO: 2;
whereby a histamine agonist in the sample is identified by measuring:
(i) substantially reduced binding of the labeled histamine or surrogate thereof to the polypeptide compared to what would
be measured in the absence of said sample in step (b); and
(ii) substantially increased level of said cellular function compared to what would be measured in the absence of said sample
in step (d);
and whereby a histamine antagonist in the sample is identified by measuring:
(i) substantially reduced binding of the labeled histamine or surrogate thereof to the polypeptide compared to what would
be measured in the absence of said sample in step (b); and
(ii) substantially similar or reduced level of said cellular function compared to what would be measured in the absence of
said sample in step (d).
|