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G PROTEIN-COUPLED RECEPTOR-G PROTEIN INTERACTIONS: A SINGLE-MOLECULE PERSPECTIVE

机译:G蛋白偶联受体-G蛋白质相互作用:单分子透视

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摘要

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.
机译:G蛋白偶联受体(GPCR)调节许多细胞和生理过程,对包括激素、神经递质、气味和光在内的多种细胞外刺激作出反应。几十年的生化和药理学研究为GPCR信号传导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蛋白偶联有了原子论上的理解。然而,GPCR和G蛋白如何在活细胞中相互作用以赋予信号传递效率和特异性仍不清楚。包括单分子显微镜在内的先进光学方法的发展为以前所未有的时空分辨率研究活细胞中的受体和G蛋白提供了手段。这些研究的结果揭示了一个意想不到的复杂程度,即GPCR之间以及与G蛋白和质膜结构元素之间发生短暂的相互作用,形成短寿命的信号纳米域,可能赋予GPCR信号的快速性和特异性。这些发现可能为药物调节GPCR功能提供新策略,最终可能为糖尿病或心力衰竭等常见疾病的创新药物铺平道路。

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