剪接体DEAH-box ATP酶的结构与功能。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
ACS Applied Bio Materials Pub Date : 2023-07-17 Print Date: 2023-07-26 DOI:10.1515/hsz-2023-0157
Marieke Enders, Piotr Neumann, Achim Dickmanns, Ralf Ficner
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引用次数: 0

摘要

前体信使核糖核酸的剪接是真核细胞的标志,由一种巨大的大分子机器剪接体进行。四种DEAH-box ATP酶是剪接体的重要组成部分,它们在剪接体激活、剪接反应、剪接的信使核糖核酸和内含子的释放以及剪接体的分解中起着重要作用。包括X射线晶体学、单粒子冷冻电子显微镜、单分子FRET和分子动力学模拟在内的综合方法为剪接体DEAH-box ATP酶的结构、动力学和功能提供了深入的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Structure and function of spliceosomal DEAH-box ATPases.

Splicing of precursor mRNAs is a hallmark of eukaryotic cells, performed by a huge macromolecular machine, the spliceosome. Four DEAH-box ATPases are essential components of the spliceosome, which play an important role in the spliceosome activation, the splicing reaction, the release of the spliced mRNA and intron lariat, and the disassembly of the spliceosome. An integrative approach comprising X-ray crystallography, single particle cryo electron microscopy, single molecule FRET, and molecular dynamics simulations provided deep insights into the structure, dynamics and function of the spliceosomal DEAH-box ATPases.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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