Molecular identification of high and low affinity receptors for nicotinic acid

被引:442
作者
Wise, A
Foord, SM
Fraser, NJ
Barnes, AA
Elshourbagy, N
Eilert, M
Ignar, DM
Murdock, PR
Steplewski, K
Green, A
Brown, AJ
Dowell, SJ
Szekeres, PG
Hassall, DG
Marshall, FH
Wilson, S
Pike, NB
机构
[1] GlaxoSmithKline, Med Res Ctr, Dept Syst Res 7TMR, Stevenage SG1 2NY, Herts, England
[2] GlaxoSmithKline, Med Res Ctr, Dept Target Bioinformat, Stevenage SG1 2NY, Herts, England
[3] GlaxoSmithKline, Med Res Ctr, Dept Gene Express & Prot Biochem, Stevenage SG1 2NY, Herts, England
[4] GlaxoSmithKline, Med Res Ctr, Dept Cellular Genom, Stevenage SG1 2NY, Herts, England
[5] GlaxoSmithKline, Med Res Ctr, Dept Cardiovasc & Urinary Ctr Excellence Drug Dis, Stevenage SG1 2NY, Herts, England
[6] GlaxoSmithKline, Metab & Viral Dis Ctr Excellence Drug Discovery, Dept Metab Dis, Res Triangle Pk, NC 27709 USA
[7] GlaxoSmithKline, Gene Cloning & Express Proteom, King Of Prussia, PA 19406 USA
关键词
D O I
10.1074/jbc.M210695200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nicotinic acid has been used clinically for over 40 years in the treatment of dyslipidemia producing a desirable normalization of a range of cardiovascular risk factors, including a marked elevation of high density lipoprotein and a reduction in mortality. The precise mechanism of action of nicotinic acid is unknown, although it is believed that activation of a G(i)-G protein-coupled receptor may contribute. Utilizing available information on the tissue distribution of nicotinic acid receptors, we identified candidate orphan receptors. The selected orphan receptors were screened for responses to nicotinic acid, in an assay for activation of G(i)-G proteins. Here we describe the identification of the G protein-coupled receptor HM74 as a low affinity receptor for nicotinic acid. We then describe the subsequent identification of HM74A in follow-up bioinformatics searches and demonstrate that it acts as a high affinity receptor for nicotinic acid and other compounds with related pharmacology. The discovery of HM74A as a molecular target for nicotinic acid may facilitate the discovery of superior drug molecules to treat dyslipidemia.
引用
收藏
页码:9869 / 9874
页数:6
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