Department of Anesthesiology, Washington University School of Medicine, St. Louis, MO, USA.
Department of Genetics, Washington University School of Medicine, St. Louis, MO, USA.
Methods Mol Biol. 2021;2268:207-221. doi: 10.1007/978-1-0716-1221-7_14.
GPCRs are responsible for activation of numerous downstream effectors. Live cell imaging of these effectors therefore provides a real-time readout of GPCR activity and allows for better understanding of temporal dynamics of GPCR-mediated signaling. Opsins, or optically activatable GPCRs, allow for these signaling pathways to be activated in a spatiotemporally precise and reversible manner. Here, we describe optogenetic methods for activating Gi, Gq, and Gs signaling pathways. Additionally, we present assays for detecting activation of these pathways in real time through live cell imaging of Gβγ translocation, PIP increase, PIP hydrolysis, cAMP production, and cell migration. These assays can be utilized for GPCR-targeted drug development, as well as for studies of a wide range of GPCR-mediated physiological processes.
G 蛋白偶联受体负责激活许多下游效应器。因此,这些效应器的活细胞成像提供了 G 蛋白偶联受体活性的实时读数,并允许更好地理解 GPCR 介导的信号转导的时间动态。视蛋白或光活化的 G 蛋白偶联受体允许以时空精确和可逆的方式激活这些信号通路。在这里,我们描述了激活 Gi、Gq 和 Gs 信号通路的光遗传学方法。此外,我们还介绍了通过活细胞成像检测 Gβγ易位、PIP 增加、PIP 水解、cAMP 产生和细胞迁移实时检测这些途径激活的测定法。这些测定法可用于针对 GPCR 的药物开发,以及用于研究广泛的 GPCR 介导的生理过程。