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首页> 外文期刊>Biochimica et biophysica acta. Biomembranes >G-protein coupled receptor structure
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G-protein coupled receptor structure

机译:G-蛋白偶联受体结构

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摘要

Because of their central role in regulation of cellular function, structure/function relationships for G-protein coupled receptors (GPCR) are of vital importance, yet only recently have sufficient data been obtained to begin mapping those relationships. GPCRs regulate a wide range of cellular processes, including the senses of taste, smell, and vision, and control a myriad of intracellular signaling systems in response to external stimuli. Many diseases are linked to GPCRs. A critical need exists for structural information to inform studies on mechanism of receptor action and regulation. X-ray crystal structures of only one GPCR, in an inactive state, have been obtained to date. However considerable structural information for a variety of GPCRs has been obtained using non-crystallographic approaches. This review begins with a review of the very earliest GPCR structural information, mostly derived from rhodopsin. Because of the difficulty in crystallizing GPCRs for X-ray crystallography, the extensive published work utilizing alternative approaches to GPCR structure is reviewed, including determination of three-dimensional structure from sparse constraints. The available X-ray crystallographic analyses on bovine rhodopsin are reviewed as the only available high-resolution structures for any GPCR. Structural information available on ligand binding to several receptors is included. The limited information on excited states of receptors is also reviewed. It is concluded that while considerable basic structural information has been obtained, more data are needed to describe the molecular mechanism of activation of a GPCR. (c) 2006 Elsevier B.V. All rights reserved.
机译:由于它们在调节细胞功能中的中心作用,G蛋白偶联受体(GPCR)的结构/功能关系至关重要,但最近仅获得了足够的数据来开始映射这些关系。 GPCRS调节各种细胞过程,包括味道,气味和视觉的感觉,并控制响应外部刺激的细胞内信号系统。许多疾病与GPCR相关联。结构信息存在危急需要,以便为受体作用和调节机制提供研究。迄今为止,已经获得了仅在非活动状态下仅一个GPCR的X射线晶体结构。然而,已经使用非晶体接近获得了各种GPCR的相当大的结构信息。本次审查开始审查最早的GPCR结构信息,主要来自罗地脂。由于难以结晶X射线晶体学的GPCR,综述了利用替代方法对GPCR结构的广泛发表的工作,包括从稀疏约束的三维结构的确定。牛罗多蛋白的可用X射线晶体分析作为任何GPCR的唯一可用的高分辨率结构进行审查。包括与几种受体结合的配体结合的结构信息。还审查了关于受体兴奋状态的有限信息。得出结论是,虽然已经获得了相当大的基本结构信息,但描述了对GPCR活化的分子机制需要更多的数据。 (c)2006 Elsevier B.v.保留所有权利。

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