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用于解析GPCR信号通路的荧光素酶报告基因检测系统

Luciferase Reporter Assay System for Deciphering GPCR Pathways.

作者信息

Cheng Zhijie, Garvin Denise, Paguio Aileen, Stecha Pete, Wood Keith, Fan Frank

机构信息

Department of Research, Promega Corporation, Madison, WI53711, USA.

出版信息

Curr Chem Genomics. 2010 Dec 21;4:84-91. doi: 10.2174/1875397301004010084.

Abstract

The G protein coupled receptors (GPCR) represent the target class for nearly half of the current therapeutic drugs and remain to be the focus of drug discovery efforts. The complexity of receptor signaling continues to evolve. It is now known that many GPCRs are coupled to multiple G-proteins, which lead to regulation of respective signaling pathways downstream. Deciphering this receptor coupling will aid our understanding of the GPCR function and ultimately developing drug candidates. Here, we report the development of four homogenous bioluminescent reporter assays using improved destabilized luciferases and various response elements: CRE, NFAT-RE, SRE, and SRF-RE. These assays allowed measurement of major GPCR pathways including cAMP production, intracellular Ca(2+) mobilizations, ERK/MAPK activ-ity, and small G protein RhoA activity, respectively using the same reporter assay format. We showed that we can decipher G protein activation profiles for exogenous m(3) muscarinic receptor and endogenous β(2)-adrenergic receptors in HEK293 cells by using these four reporter assays. Furthermore, we demonstrated that these assays can be readily used for potency rankings of agonists and antagonists, and for high throughput screening.

摘要

G蛋白偶联受体(GPCR)是目前近一半治疗药物的靶点类别,并且仍然是药物研发工作的重点。受体信号传导的复杂性仍在不断演变。现在已知许多GPCR与多种G蛋白偶联,这会导致下游各自信号通路的调节。解读这种受体偶联将有助于我们理解GPCR的功能,并最终开发候选药物。在此,我们报告了使用改进的不稳定荧光素酶和各种反应元件(CRE、NFAT-RE、SRE和SRF-RE)开发的四种均相生物发光报告基因检测方法。这些检测方法能够分别使用相同的报告基因检测形式来测量主要的GPCR信号通路,包括cAMP生成、细胞内Ca(2+) 动员、ERK/MAPK活性和小G蛋白RhoA活性。我们表明,通过使用这四种报告基因检测方法,我们能够解读HEK293细胞中外源m(3) 毒蕈碱受体和内源性β(2)-肾上腺素能受体的G蛋白激活谱。此外,我们证明这些检测方法可轻松用于激动剂和拮抗剂的效价排名以及高通量筛选。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d15e/3040460/90ab957183cb/TOCHGENJ-4-84_F1.jpg

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