Kim Hyunbin, Baek In-Yeop, Seong Jihye
Brain Science Institute, Korea Institute of Science and Technology (KIST), Seoul, South Korea.
Division of Bio-Medical Science and Technology, KIST School, Korea University of Science and Technology, Seoul, South Korea.
Front Cell Dev Biol. 2022 Sep 29;10:1007893. doi: 10.3389/fcell.2022.1007893. eCollection 2022.
G protein-coupled receptors (GPCRs) regulate a wide range of physiological and pathophysiological cellular processes, thus it is important to understand how GPCRs are activated and function in various cellular contexts. In particular, the activation process of GPCRs is dynamically regulated upon various extracellular stimuli, and emerging evidence suggests the subcellular functions of GPCRs at endosomes and other organelles. Therefore, precise monitoring of the GPCR activation process with high spatiotemporal resolution is required to investigate the underlying molecular mechanisms of GPCR functions. In this review, we will introduce genetically encoded fluorescent biosensors that can precisely monitor the real-time GPCR activation process in live cells. The process includes the binding of extracellular GPCR ligands, conformational change of GPCR, recruitment of G proteins or β-arrestin, GPCR internalization and trafficking, and the GPCR-related downstream signaling events. We will introduce fluorescent GPCR biosensors based on a variety of strategies such as fluorescent resonance energy transfer (FRET), bioluminescence resonance energy transfer (BRET), circular permuted fluorescent protein (cpFP), and nanobody. We will discuss the pros and cons of these GPCR biosensors as well as their applications in GPCR research.
G蛋白偶联受体(GPCRs)调节广泛的生理和病理生理细胞过程,因此了解GPCRs在各种细胞环境中如何被激活和发挥功能非常重要。特别是,GPCRs的激活过程在各种细胞外刺激下受到动态调节,并且新出现的证据表明GPCRs在内体和其他细胞器中的亚细胞功能。因此,需要以高时空分辨率精确监测GPCR激活过程,以研究GPCR功能的潜在分子机制。在这篇综述中,我们将介绍可精确监测活细胞中实时GPCR激活过程的基因编码荧光生物传感器。该过程包括细胞外GPCR配体的结合、GPCR的构象变化、G蛋白或β-抑制蛋白的募集、GPCR内化和运输以及与GPCR相关的下游信号事件。我们将介绍基于多种策略的荧光GPCR生物传感器,如荧光共振能量转移(FRET)、生物发光共振能量转移(BRET)、环形排列荧光蛋白(cpFP)和纳米抗体。我们将讨论这些GPCR生物传感器的优缺点及其在GPCR研究中的应用。