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从荧光光谱和成像推断 GPCR 信号转导的物理生物学。

Physical biology of GPCR signalling dynamics inferred from fluorescence spectroscopy and imaging.

机构信息

Section Molecular Cytology, Swammerdam Institute for Life Sciences, University of Amsterdam, Science Park 904, NL-1098 XH, Amsterdam, The Netherlands; Section Systems Bioinformatics, Amsterdam Institute for Molecules, Medicines and Systems, VU University, De Boelelaan 1085, NL-1081 HV, Amsterdam, The Netherlands.

Section Molecular Cytology, Swammerdam Institute for Life Sciences, University of Amsterdam, Science Park 904, NL-1098 XH, Amsterdam, The Netherlands.

出版信息

Curr Opin Struct Biol. 2019 Apr;55:204-211. doi: 10.1016/j.sbi.2019.05.007. Epub 2019 Jul 15.

Abstract

The physical biology of G protein-coupled receptor (GPCR) signalling can be inferred from imaging of single molecules and single living cells. In this opinion paper, we highlight recent developments in technologies to study GPCR signalling in vitro and in cyto. We start from mobility and localisation characteristics of single receptors in membranes. Subsequently, we discuss the kinetics of shifts in receptor-conformation equilibrium due to allosteric binding events and G protein activation. We continue with recent insights into downstream signalling and the role of delayed negative feedback to suppress GPCR signalling. Finally, we discuss new strategies to reveal how the multiplex signalling responses of cells to ligand mixtures, mediated by their entire receptor arsenal, can be disentangled, using single-cell data.

摘要

G 蛋白偶联受体 (GPCR) 信号的物理生物学可以通过对单个分子和单个活细胞的成像来推断。在本观点文章中,我们重点介绍了研究体外和细胞内 GPCR 信号的新技术的最新进展。我们从单个受体在膜中的流动性和定位特征开始。随后,我们讨论了由于变构结合事件和 G 蛋白激活导致受体构象平衡变化的动力学。接下来,我们探讨了下游信号传递的最新见解,以及延迟负反馈在抑制 GPCR 信号中的作用。最后,我们讨论了新的策略,以揭示如何使用单细胞数据来揭示细胞对配体混合物的多重信号响应,这些响应是由其整个受体库介导的。

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