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揭示靶向 G 蛋白偶联受体结构与功能的研究路径。

Illuminating the Path to Target GPCR Structures and Functions.

机构信息

Imperial College London, White City Campus, Molecular Sciences Research Hub, 80 Wood Lane, London W12 0BZ, U.K.

Department of Biological Sciences, National University of Singapore, 14 Science Drive 4, Singapore 117543.

出版信息

Biochemistry. 2020 Oct 13;59(40):3783-3795. doi: 10.1021/acs.biochem.0c00606. Epub 2020 Sep 29.

Abstract

G-Protein-coupled receptors (GPCRs) are ubiquitous within eukaryotes, responsible for a wide array of physiological and pathological processes. Indeed, the fact that they are the most drugged target in the human genome is indicative of their importance. Despite the clear interest in GPCRs, most information regarding their activity has been so far obtained by analyzing the response from a "bulk medium". As such, this Perspective summarizes some of the common methods for this indirect observation. Nonetheless, by inspecting approaches applying super-resolution imaging, we argue that imaging is perfectly situated to obtain more detailed structural and spatial information, assisting in the development of new GPCR-targeted drugs and clinical strategies. The benefits of direct optical visualization of GPCRs are analyzed in the context of potential future directions in the field.

摘要

G 蛋白偶联受体(GPCRs)在真核生物中普遍存在,负责广泛的生理和病理过程。事实上,它们是人类基因组中被药物靶向最多的目标,这表明了它们的重要性。尽管人们对 GPCR 有着浓厚的兴趣,但迄今为止,大多数关于它们活性的信息都是通过分析“总体介质”的反应获得的。因此,本文总结了一些用于这种间接观察的常见方法。尽管如此,通过检查应用超分辨率成像的方法,我们认为成像非常适合获取更详细的结构和空间信息,有助于开发新的 GPCR 靶向药物和临床策略。本文还分析了直接光学可视化 GPCR 的优势,探讨了该领域未来可能的发展方向。

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