Institute of Metabolism and Systems Research, University of Birmingham, Birmingham, United Kingdom; Centre of Membrane Proteins and Receptors (COMPARE), Universities of Nottingham and Birmingham, Birmingham, United Kingdom.
Physiol Rev. 2021 Jul 1;101(3):857-906. doi: 10.1152/physrev.00021.2020. Epub 2020 Dec 17.
G protein-coupled receptors (GPCRs) regulate many cellular and physiological processes, responding to a diverse range of extracellular stimuli including hormones, neurotransmitters, odorants, and light. Decades of biochemical and pharmacological studies have provided fundamental insights into the mechanisms of GPCR signaling. Thanks to recent advances in structural biology, we now possess an atomistic understanding of receptor activation and G protein coupling. However, how GPCRs and G proteins interact in living cells to confer signaling efficiency and specificity remains insufficiently understood. The development of advanced optical methods, including single-molecule microscopy, has provided the means to study receptors and G proteins in living cells with unprecedented spatio-temporal resolution. The results of these studies reveal an unexpected level of complexity, whereby GPCRs undergo transient interactions among themselves as well as with G proteins and structural elements of the plasma membrane to form short-lived signaling nanodomains that likely confer both rapidity and specificity to GPCR signaling. These findings may provide new strategies to pharmaceutically modulate GPCR function, which might eventually pave the way to innovative drugs for common diseases such as diabetes or heart failure.
G 蛋白偶联受体(GPCRs)调节许多细胞和生理过程,对包括激素、神经递质、气味和光在内的各种细胞外刺激作出反应。几十年来的生化和药理学研究为 GPCR 信号转导的机制提供了基本的见解。由于结构生物学的最新进展,我们现在对受体激活和 G 蛋白偶联有了原子水平的理解。然而,GPCRs 和 G 蛋白在活细胞中如何相互作用以赋予信号效率和特异性仍了解不足。先进光学方法的发展,包括单分子显微镜,为在活细胞中以空前的时空分辨率研究受体和 G 蛋白提供了手段。这些研究的结果揭示了一种出人意料的复杂性,即 GPCR 会在它们之间以及与 G 蛋白和质膜的结构元件之间发生短暂的相互作用,形成短暂存在的信号纳米域,这可能为 GPCR 信号转导提供快速性和特异性。这些发现可能为药物调节 GPCR 功能提供新的策略,最终可能为糖尿病或心力衰竭等常见疾病开辟创新药物的道路。