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通过综合结构-动力学方法实现对动态蛋白质相互作用的广泛分子见解。

Achieving broad molecular insights into dynamic protein interactions by integrated structural-kinetic approaches.

机构信息

Departments of Structural Biology and Biological Regulation, The Weizmann Institute of Science, Rehovot 76100, Israel.

出版信息

Curr Opin Struct Biol. 2011 Oct;21(5):678-85. doi: 10.1016/j.sbi.2011.07.008. Epub 2011 Sep 22.

Abstract

A network of dynamic protein interactions with their protein partners, substrates, and ligands is known to be crucial for biological function. Revealing molecular and structural-based mechanisms at atomic resolution and in real-time is fundamental for achieving a basic understanding of cellular processes. These technically challenging goals may be achieved by combining time-resolved spectroscopic and structural-kinetic tools, thus providing broad insights into specific molecular events over a wide range of timescales. Here we review representative studies utilizing such an integrated real-time structural approach designed to reveal molecular mechanisms underlying protein interactions at atomic resolution.

摘要

动态蛋白质相互作用网络及其蛋白质伴侣、底物和配体对于生物功能至关重要。在原子分辨率和实时水平上揭示基于分子和结构的机制对于实现对细胞过程的基本理解是至关重要的。这些具有技术挑战性的目标可以通过结合时间分辨光谱和结构动力学工具来实现,从而在广泛的时间范围内提供对特定分子事件的广泛了解。在这里,我们回顾了利用这种集成的实时结构方法的代表性研究,旨在揭示原子分辨率下蛋白质相互作用的分子机制。

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