解读GPCR途径的荧光素酶报告基因检测系统。

Zhijie Cheng, Denise Garvin, Aileen Paguio, Pete Stecha, Keith Wood, Frank Fan
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引用次数: 147

摘要

G蛋白偶联受体(GPCR)代表了目前近一半的治疗药物的靶标类别,并且仍然是药物发现工作的重点。受体信号的复杂性在不断进化。现在已知许多gpcr与多种g蛋白偶联,导致各自下游信号通路的调节。破译这种受体偶联将有助于我们了解GPCR的功能,并最终开发候选药物。在这里,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)开发的四种均质生物发光报告基因检测方法。这些实验允许测量主要的GPCR途径,包括cAMP产生,细胞内Ca(2+)动员,ERK/MAPK活性和小G蛋白RhoA活性,分别使用相同的报告分析格式。我们发现,通过这四种报告基因检测,我们可以破译HEK293细胞中外源性m(3)毒毒碱受体和内源性β(2)-肾上腺素能受体的G蛋白激活谱。此外,我们证明了这些检测可以很容易地用于激动剂和拮抗剂的效力排名,并用于高通量筛选。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Luciferase Reporter Assay System for Deciphering GPCR Pathways.

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.

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