用时间依赖性浸泡-触发-冷冻x射线晶体学观察细菌RNA聚合酶转录反应。

Q3 Biochemistry, Genetics and Molecular Biology
Enzymes Pub Date : 2021-01-01 Epub Date: 2021-07-24 DOI:10.1016/bs.enz.2021.06.009
Yeonoh Shin, Katsuhiko S Murakami
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引用次数: 1

摘要

RNA聚合酶(RNA polymerase, RNAP)是基因表达的中心酶,将DNA转录为RNA。除了线粒体RNA转录是由单亚基RNAP进行外,所有细胞生物都通过高度保守的多亚基dna依赖性RNAP合成RNA。60多年来的广泛研究已经阐明了细胞rnap的结构和功能。在这篇综述中,我们介绍了细菌RNAP的简单结构特征,这是表征最清楚的模型酶,以及一种新的实验方法,即“时间依赖的浸泡-触发-冻结x射线晶体学”,可以在原子分辨率下实时观察RNA合成反应。这一原理方法可用于阐明细胞RNAP转录的基本机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Watching the bacterial RNA polymerase transcription reaction by time-dependent soak-trigger-freeze X-ray crystallography.

RNA polymerase (RNAP) is the central enzyme of gene expression, which transcribes DNA to RNA. All cellular organisms synthesize RNA with highly conserved multi-subunit DNA-dependent RNAPs, except mitochondrial RNA transcription, which is carried out by a single-subunit RNAP. Over 60 years of extensive research has elucidated the structures and functions of cellular RNAPs. In this review, we introduce a brief structural feature of bacterial RNAP, the most well characterized model enzyme, and a novel experimental approach known as "Time-dependent soak-trigger-freeze X-ray crystallography" which can be used to observe the RNA synthesis reaction at atomic resolution in real time. This principle methodology can be used for elucidating fundamental mechanisms of cellular RNAP transcription.

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来源期刊
Enzymes
Enzymes Biochemistry, Genetics and Molecular Biology-Biotechnology
CiteScore
4.30
自引率
0.00%
发文量
10
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