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与工程化小G蛋白结合的腺苷A受体的表达、纯化及结晶

Expression, Purification and Crystallisation of the Adenosine A Receptor Bound to an Engineered Mini G Protein.

作者信息

Carpenter Byron, Tate Christopher G

机构信息

MRC Laboratory of Molecular Biology, Cambridge Biomedical Campus, Francis Crick Avenue, Cambridge, UK.

出版信息

Bio Protoc. 2017 Apr 20;7(8). doi: 10.21769/BioProtoc.2234.

Abstract

G protein-coupled receptors (GPCRs) promote cytoplasmic signalling by activating heterotrimeric G proteins in response to extracellular stimuli such as light, hormones and nucleosides. Structure determination of GPCR-G protein complexes is central to understanding the precise mechanism of signal transduction. However, these complexes are challenging targets for structural studies due to their conformationally dynamic and inherently transient nature. We recently developed an engineered G protein, mini-G, which addressed these problems and allowed the formation of a stable GPCR-G protein complex. Mini-G facilitated the structure determination of the human adenosine A receptor (AR) in its G protein-bound conformation at 3.4 Å resolution. Here, we describe a step by step protocol for the expression and purification of AR, and crystallisation of the AR-mini-G complex.

摘要

G蛋白偶联受体(GPCRs)通过响应光、激素和核苷等细胞外刺激激活异源三聚体G蛋白来促进细胞质信号传导。GPCR-G蛋白复合物的结构测定是理解信号转导精确机制的核心。然而,由于其构象动态性和固有的短暂性,这些复合物是结构研究的挑战性目标。我们最近开发了一种工程化G蛋白mini-G,它解决了这些问题,并允许形成稳定的GPCR-G蛋白复合物。Mini-G有助于以3.4 Å分辨率确定处于与G蛋白结合构象的人腺苷A受体(AR)的结构。在这里,我们描述了AR的表达和纯化以及AR-mini-G复合物结晶的逐步方案。

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