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利用交联来研究核糖体动力学。

Using Cross-links to Study Ribosomal Dynamics.

作者信息

Ivanov Valery I, Mears Jason A

机构信息

a V.A. Engelhardt Institute of Molecular Biology Russian Academy of Sciences , 119991 , Moscow , Russia.

出版信息

J Biomol Struct Dyn. 2004 Jun;21(6):691-698. doi: 10.1080/07391102.2004.10506962.

Abstract

Abstract After publications of 3-D models of a static ribosome and its large and small subunits, one of the next tasks is to recognize movable ribosomal elements responsible for mechanical shifts during protein synthesis. Statistic analysis of available cross-linking data allowed us to reveal three well separated groups of motions in the ribosome: I, mean magnitude of 10Å; II, most abundant, centered at 20Å and of wide dispersion, and III, sparsely populated, with large distances up to 95Å. The last group, III, comprises elements, like the L7/12-stalk and the L1- protuberance, that adopt different positions in crystallographic or electron micrographic structures, and neighboring hairpins 88 and 89, indicating mobility. We demonstrate that the cross- linking method can be applied to study ribosomal dynamics, including large-scale functional movements and, in particular, to estimate which structures participate in molecular switches.

摘要

摘要 在静态核糖体及其大小亚基的三维模型发表之后,接下来的任务之一是识别在蛋白质合成过程中负责机械移位的可移动核糖体元件。对现有交联数据的统计分析使我们能够揭示核糖体中三个明显分开的运动组:I组,平均幅度为10Å;II组,最为丰富,以20Å为中心且分散范围广;III组,分布稀疏,距离可达95Å。最后一组,即III组,包括L7/12柄和L1突起等元件,它们在晶体学或电子显微镜结构中占据不同位置,以及相邻的发夹88和89,表明存在移动性。我们证明交联方法可用于研究核糖体动力学,包括大规模功能运动,特别是用于估计哪些结构参与分子开关。

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