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视锥蛋白抑制素2.3埃分辨率的晶体结构:受体特异性的演变

Crystal structure of cone arrestin at 2.3A: evolution of receptor specificity.

作者信息

Sutton R Bryan, Vishnivetskiy Sergey A, Robert Justin, Hanson Susan M, Raman Dayanidhi, Knox Barry E, Kono Masahiro, Navarro Javier, Gurevich Vsevolod V

机构信息

Department of Neuroscience and Cell Biology, University of Texas Medical Branch, and Sealy Center for Molecular Science & Structural Biology, Galveston, TX 77555, USA.

出版信息

J Mol Biol. 2005 Dec 16;354(5):1069-80. doi: 10.1016/j.jmb.2005.10.023. Epub 2005 Nov 2.

Abstract

Arrestins play a fundamental role in the regulation and signal transduction of G protein-coupled receptors. Here we describe the crystal structure of cone arrestin at 2.3A resolution. The overall structure of cone visual arrestin is similar to the crystal structures of rod visual and the non-visual arrestin-2, consisting of two domains, each containing ten beta-sheets. However, at the tertiary structure level, there are two major differences, in particular on the concave surfaces of the two domains implicated in receptor binding and in the loop between beta-strands I and II. Functional analysis shows that cone arrestin, in sharp contrast to its rod counterpart, bound cone pigments and non-visual receptors. Conversely, non-visual arrestin-2 bound cone pigments, suggesting that it may also regulate phototransduction and/or photopigment trafficking in cone photoreceptors. These findings indicate that cone arrestin displays structural and functional features intermediate between the specialized rod arrestin and the non-visual arrestins, which have broad receptor specificity. A unique functional feature of cone arrestin was the low affinity for its cognate receptor, resulting in an unusually rapid dissociation of the complex. Transient arrestin binding to the photopigment in cones may be responsible for the extremely rapid regeneration and reuse of the photopigment that is essential for cone function at high levels of illumination.

摘要

抑制蛋白在G蛋白偶联受体的调节和信号转导中发挥着重要作用。在此,我们描述了视锥细胞抑制蛋白在2.3埃分辨率下的晶体结构。视锥细胞视觉抑制蛋白的整体结构与视杆细胞视觉抑制蛋白和非视觉抑制蛋白-2的晶体结构相似,由两个结构域组成,每个结构域包含十个β折叠。然而,在三级结构水平上,存在两个主要差异,特别是在与受体结合相关的两个结构域的凹面以及β链I和II之间的环上。功能分析表明,与视杆细胞抑制蛋白形成鲜明对比的是,视锥细胞抑制蛋白能结合视锥色素和非视觉受体。相反,非视觉抑制蛋白-2能结合视锥色素,这表明它也可能调节视锥光感受器中的光转导和/或光色素运输。这些发现表明,视锥细胞抑制蛋白呈现出介于具有广泛受体特异性的特殊视杆细胞抑制蛋白和非视觉抑制蛋白之间的结构和功能特征。视锥细胞抑制蛋白的一个独特功能特征是对其同源受体的亲和力较低,导致复合物异常快速解离。视锥细胞中抑制蛋白与光色素的短暂结合可能是光色素快速再生和再利用的原因,而光色素的快速再生和再利用对于视锥细胞在高光照水平下的功能至关重要。

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