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仅由蛋白质组成的核糖核酸酶 P 酶进行 RNA 加工的结构和机制基础。

Structural and mechanistic basis of RNA processing by protein-only ribonuclease P enzymes.

机构信息

Department of Cellular Biochemistry, University Medical Center Goettingen, Humboldtallee 23, D-37073 Goettingen, Germany; Research Group Structure and Function of Molecular Machines, Max Planck Institute for Multidisciplinary Sciences, Am Fassberg 11, D-37077 Goettingen, Germany.

Department of Cellular Biochemistry, University Medical Center Goettingen, Humboldtallee 23, D-37073 Goettingen, Germany; Research Group Structure and Function of Molecular Machines, Max Planck Institute for Multidisciplinary Sciences, Am Fassberg 11, D-37077 Goettingen, Germany; Cluster of Excellence Multiscale Bioimaging: from Molecular Machines to Networks of Excitable Cells (MBExC), University of Goettingen, D-37075 Goettingen, Germany.

出版信息

Trends Biochem Sci. 2022 Nov;47(11):965-977. doi: 10.1016/j.tibs.2022.05.006. Epub 2022 Jun 18.

Abstract

Ribonuclease P (RNase P) enzymes are responsible for the 5' processing of tRNA precursors. In addition to the well-characterised ribozyme-based RNase P enzymes, an evolutionarily distinct group of protein-only RNase Ps exists. These proteinaceous RNase Ps (PRORPs) can be found in all three domains of life and can be divided into two structurally different types: eukaryotic and prokaryotic. Recent structural studies on members of both families reveal a surprising diversity of molecular architectures, but also highlight conceptual and mechanistic similarities. Here, we provide a comparison between the different types of PRORP enzymes and review how the combination of structural, biochemical, and biophysical studies has led to a molecular picture of protein-mediated tRNA processing.

摘要

核糖核酸酶 P(RNase P)酶负责 tRNA 前体的 5'加工。除了具有良好特征的基于核酶的 RNase P 酶之外,还存在一组进化上不同的仅由蛋白质组成的 RNase P。这些蛋白质 RNase P(PRORP)可以在所有三个生命领域中找到,并可以分为两种结构不同的类型:真核生物和原核生物。最近对这两个家族成员的结构研究揭示了分子结构的惊人多样性,但也突出了概念和机制上的相似性。在这里,我们比较了不同类型的 PRORP 酶,并回顾了结构,生化和生物物理研究的结合如何导致蛋白质介导的 tRNA 加工的分子图景。

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