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BUNDLE:一个用于构建G蛋白偶联受体跨膜结构域的程序。

BUNDLE: a program for building the transmembrane domains of G-protein-coupled receptors.

作者信息

Filizola M, Perez J J, Cartenì-Farina M

机构信息

Departament d'Enginyeria Química, UPC, ETS d'Enginyers Industrials, Barcelona, Spain.

出版信息

J Comput Aided Mol Des. 1998 Mar;12(2):111-8. doi: 10.1023/a:1007969112988.

Abstract

The only information available at present about the structural features of G-protein-coupled receptors (GPCRs) comes from low resolution electron density maps of rhodopsin obtained from electron microscopy studies on 2D crystals. Despite their low resolution, maps can be used to extract information about transmembrane helix relative positions and their tilt. This information, together with a reliable algorithm to assess the residues involved in each of the membrane spanning regions, can be used to construct a 3D model of the transmembrane domains of rhodopsin at atomic resolution. In the present work, we describe an automated procedure applicable to generate such a model and, in general, to construct a 3D model of any given GPCR with the only assumption that it adopts the same helix arrangement as in rhodopsin. The present approach avoids uncertainties associated with other procedures available for constructing models of GPCRs based on a template, since sequence identity among GPCRs of different families in most of the cases is not significant. The steps involved in the construction of the model are: (i) locate the centers of the helices according to the low-resolution electron density map; (ii) compute the tilt of each helix based on the elliptical shape observed by each helix in the map; (iii) define a local coordinate system for each of the helices; (iv) bring them together in an antiparallel orientation; (v) rotate each helix through the helical axis in such a way that its hydrophobic moment points in the same direction of the bisector formed between three consecutive helices in the bundle; (vi) rotate each helix through an axis perpendicular to the helical one to assign a proper tilt; and (vii) translate each helix to its center deduced from the projection map.

摘要

目前关于G蛋白偶联受体(GPCRs)结构特征的唯一可用信息来自于通过二维晶体电子显微镜研究获得的视紫红质低分辨率电子密度图。尽管分辨率较低,但这些图可用于提取有关跨膜螺旋相对位置及其倾斜度的信息。该信息与一种可靠的算法相结合,该算法用于评估每个跨膜区域中涉及的残基,可用于构建原子分辨率的视紫红质跨膜结构域的三维模型。在本工作中,我们描述了一种自动化程序,适用于生成这样的模型,并且一般来说,在唯一的假设即它采用与视紫红质相同的螺旋排列的情况下,构建任何给定GPCR的三维模型。本方法避免了与基于模板构建GPCR模型的其他程序相关的不确定性,因为在大多数情况下,不同家族的GPCR之间的序列同一性并不显著。构建模型所涉及的步骤如下:(i)根据低分辨率电子密度图确定螺旋的中心;(ii)根据图中每个螺旋观察到的椭圆形状计算每个螺旋的倾斜度;(iii)为每个螺旋定义一个局部坐标系;(iv)以反平行方向将它们组合在一起;(v)使每个螺旋绕螺旋轴旋转,使得其疏水矩指向束中三个连续螺旋之间形成的平分线的相同方向;(vi)使每个螺旋绕垂直于螺旋轴的轴旋转以赋予适当的倾斜度;以及(vii)将每个螺旋平移到从投影图推导得出的其中心位置。

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