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蛋白质构象异质性状态的测定

Determination of conformationally heterogeneous states of proteins.

作者信息

Vendruscolo Michele

机构信息

Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, UK.

出版信息

Curr Opin Struct Biol. 2007 Feb;17(1):15-20. doi: 10.1016/j.sbi.2007.01.002. Epub 2007 Jan 18.

Abstract

Although conformationally heterogeneous states of proteins are involved in a range of important biological processes, including protein folding and misfolding, and signal transduction, detailed knowledge of their structure and dynamics is still largely missing. Proteins in many of these states are constantly changing shape, such that they are better described as ensembles of conformations rather than in terms of well-defined structures, as is normally the case for native states. Methods in which molecular simulations are combined with experimental measurements are emerging as a powerful route to the accurate determination of the conformational properties of these states of proteins.

摘要

尽管蛋白质的构象异质状态参与了一系列重要的生物学过程,包括蛋白质折叠与错误折叠以及信号转导,但我们对其结构和动力学的详细了解仍然十分匮乏。处于许多这类状态的蛋白质不断改变形状,以至于将它们描述为构象集合体比用通常描述天然状态的明确定义结构更为合适。将分子模拟与实验测量相结合的方法正成为准确测定蛋白质这些状态构象性质的有力途径。

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