Demby Alexander, Zaccolo Manuela
Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, United Kingdom.
Front Physiol. 2024 Jan 8;14:1310197. doi: 10.3389/fphys.2023.1310197. eCollection 2023.
G protein-coupled receptors (GPCRs) are the most frequent target of currently approved drugs and play a central role in both physiological and pathophysiological processes. Beyond the canonical understanding of GPCR signal transduction, the importance of receptor conformation, beta-arrestin (β-arr) biased signalling, and signalling from intracellular locations other than the plasma membrane is becoming more apparent, along with the tight spatiotemporal compartmentalisation of downstream signals. Fluorescent and bioluminescent biosensors have played a pivotal role in elucidating GPCR signalling events in live cells. To understand the mechanisms of action of the GPCR-targeted drugs currently available, and to develop new and better GPCR-targeted therapeutics, understanding these novel aspects of GPCR signalling is critical. In this review, we present some of the tools available to interrogate each of these features of GPCR signalling, we illustrate some of the key findings which have been made possible by these tools and we discuss their limitations and possible developments.
G蛋白偶联受体(GPCRs)是目前已获批药物最常见的靶点,在生理和病理生理过程中均发挥着核心作用。除了对GPCR信号转导的传统认识外,受体构象、β-抑制蛋白(β-arr)偏向性信号传导以及质膜以外细胞内位置的信号传导的重要性日益凸显,同时下游信号的紧密时空分隔也愈发明显。荧光和生物发光生物传感器在阐明活细胞中GPCR信号事件方面发挥了关键作用。为了理解目前可用的GPCR靶向药物的作用机制,并开发新的、更好的GPCR靶向治疗药物,了解GPCR信号传导的这些新方面至关重要。在这篇综述中,我们介绍了一些可用于探究GPCR信号传导各特征的工具,阐述了通过这些工具已取得的一些关键发现,并讨论了它们的局限性和可能的发展方向。