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用于G蛋白偶联受体脱敏和再敏化的基于细胞的自检分析方法

Self-Checking Cell-Based Assays for GPCR Desensitization and Resensitization.

作者信息

Fisher Gregory W, Fuhrman Margaret H, Adler Sally A, Szent-Gyorgyi Christopher, Waggoner Alan S, Jarvik Jonathan W

机构信息

Department of Biological Sciences and Molecular Biosensor and Imaging Center, Carnegie Mellon University, Pittsburgh, PA, USA.

Department of Biological Sciences and Molecular Biosensor and Imaging Center, Carnegie Mellon University, Pittsburgh, PA, USA

出版信息

J Biomol Screen. 2014 Sep;19(8):1220-6. doi: 10.1177/1087057114534299. Epub 2014 May 12.

Abstract

G protein-coupled receptors (GPCRs) play stimulatory or modulatory roles in numerous physiological states and processes, including growth and development, vision, taste and olfaction, behavior and learning, emotion and mood, inflammation, and autonomic functions such as blood pressure, heart rate, and digestion. GPCRs constitute the largest protein superfamily in the human and are the largest target class for prescription drugs, yet most are poorly characterized, and of the more than 350 nonolfactory human GPCRs, over 100 are orphans for which no endogenous ligand has yet been convincingly identified. We here describe new live-cell assays that use recombinant GPCRs to quantify two general features of GPCR cell biology-receptor desensitization and resensitization. The assays employ a fluorogen-activating protein (FAP) reporter that reversibly complexes with either of two soluble organic molecules (fluorogens) whose fluorescence is strongly enhanced when complexed with the FAP. Both assays require no wash or cleanup steps and are readily performed in microwell plates, making them adaptable to high-throughput drug discovery applications.

摘要

G蛋白偶联受体(GPCRs)在众多生理状态和过程中发挥刺激或调节作用,包括生长发育、视觉、味觉和嗅觉、行为与学习、情绪和心境、炎症以及诸如血压、心率和消化等自主功能。GPCRs是人类中最大的蛋白质超家族,也是处方药的最大靶点类别,但大多数GPCRs的特征尚不明确,在350多种非嗅觉人类GPCRs中,有100多种是孤儿受体,尚未令人信服地鉴定出其内源性配体。我们在此描述了新的活细胞分析方法,该方法使用重组GPCRs来量化GPCR细胞生物学的两个一般特征——受体脱敏和再敏化。这些分析方法采用一种荧光激活蛋白(FAP)报告基因,它与两种可溶性有机分子(荧光原)中的任何一种可逆结合,当与FAP结合时,其荧光会强烈增强。这两种分析方法都不需要洗涤或清理步骤,并且很容易在微孔板中进行,使其适用于高通量药物发现应用。

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