分离gpcr的生物物理解剖:历史下的腺苷A2A受体

J. Banères, Thomas Botzanowski, J. Boutin, Barbara Calamini, Jérôme Castel, L. Catoire, S. Cianférani, C. Demesmay, G. Ferguson, G. Ferry, J. Kniazeff, I. Krimm, Thierry Langer, G. Lebon, M. Ley, M. Nyerges, Magali Schwob, C. Vénien-Bryan, R. Wagner, G. Zeder‐Lutz, Claudia Zilian-Stohrer
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引用次数: 0

摘要

为了提供用于研究g蛋白偶联受体的生物物理方法的概述,我们选择考虑腺苷A2A受体作为模型,因为它在文献中广泛报道,以探索gpcr的研究方式。在简要介绍受体后,我们收集了用于研究A2A受体的药理学和结构的各种工具的描述。我们首先描述了导致gpcr研究成功的关键进展,包括A2A的克隆、表达和纯化,以及随后的表征,包括质量控制、结合和功能研究,这些都是进一步了解受体所必需的。然后,我们回顾了A2A纳米片的重构,以及这种生物材料在结构质谱、核磁共振、量热法和各种其他方法中的应用,不仅获得了有关A2A结构和功能的信息,而且还获得了受体的动力学和进行此类研究所需的工具。本文提出的技术主体适用于所有适合纯化的gpcr。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biophysical Dissection of Isolated GPCRs: The Adenosine A2A Receptor under the Bistouries
In an effort to provide an overview of the biophysical approaches used to study G-protein-coupled receptors, we chose to consider the adenosine A2A receptor as a model, as it is widely reported in the literature to explore the way GPCRs are studied nowadays. After a brief introduction of the receptor, we gathered descriptions of the various tools used to investigate the pharmacology and structure of the A2A receptor. We began by describing the key developments which have led to successful studies of GPCRs including the cloning, expression and purification of A2A, and the subsequent characterizations including quality control, binding and functional studies that have been necessary for the further understanding of the receptor. Then, we reviewed the reconstitution of A2A into nanodiscs as well as the use of this biological material in structural mass spectrometry, NMR, calorimetry and various other approaches to gain not only information about the structure and function of A2A, but also the dynamics of the receptor and the tools necessary to pursue such investigations. The body of techniques presented herein are applicable to all GPCRs amenable to purification.
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