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人腺苷A(2A)受体热稳定激动剂结合构象的纯化与结晶

Purification and Crystallization of a Thermostabilized Agonist-Bound Conformation of the Human Adenosine A(2A) Receptor.

作者信息

Tate Christopher G, Lebon Guillaume

机构信息

MRC Laboratory of Molecular Biology, Cambridge Biomedical Campus, Francis Crick Avenue, Cambridge, CB2 0QH, UK,

出版信息

Methods Mol Biol. 2015;1335:17-27. doi: 10.1007/978-1-4939-2914-6_2.

Abstract

Crystallization of G protein-coupled receptors (GPCRs) is successful due to the development of generic protein engineering strategies, which has resulted in the structure determination of more than 25 GPCRs, including representatives from class A, B, C, and F. Most of the X-ray structures available correspond to an inactive conformation of the receptor bound to an antagonist. Only a few high-resolution structures of agonist-bound conformations of GPCRs have been determined over the last 6 years. Here, we describe the purification and crystallization protocols of a thermostabilized agonist-bound conformation of the human adenosine A2A receptor.

摘要

由于通用蛋白质工程策略的发展,G蛋白偶联受体(GPCRs)的结晶取得了成功,这使得超过25种GPCRs的结构得以确定,包括A、B、C和F类的代表。目前可用的大多数X射线结构对应于与拮抗剂结合的受体的非活性构象。在过去6年中,仅确定了少数GPCRs激动剂结合构象的高分辨率结构。在此,我们描述了人腺苷A2A受体热稳定激动剂结合构象的纯化和结晶方案。

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