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病毒RNA依赖性RNA聚合反应的起始

Initiation of viral RNA-dependent RNA polymerization.

作者信息

van Dijk Alberdina A, Makeyev Eugene V, Bamford Dennis H

机构信息

Institute of Biotechnology and Faculty of Biosciences, PO Box 56, Viikinkaari 5, FIN-00014 University of Helsinki, Finland.

出版信息

J Gen Virol. 2004 May;85(Pt 5):1077-1093. doi: 10.1099/vir.0.19731-0.

Abstract

This review summarizes the combined insights from recent structural and functional studies of viral RNA-dependent RNA polymerases (RdRPs) with the primary focus on the mechanisms of initiation of RNA synthesis. Replication of RNA viruses has traditionally been approached using a combination of biochemical and genetic methods. Recently, high-resolution structures of six viral RdRPs have been determined. For three RdRPs, enzyme complexes with metal ions, single-stranded RNA and/or nucleoside triphosphates have also been solved. These advances have expanded our understanding of the molecular mechanisms of viral RNA synthesis and facilitated further RdRP studies by informed site-directed mutagenesis. What transpires is that the basic polymerase right hand shape provides the correct geometrical arrangement of substrate molecules and metal ions at the active site for the nucleotidyl transfer catalysis, while distinct structural elements have evolved in the different systems to ensure efficient initiation of RNA synthesis. These elements feed the template, NTPs and ions into the catalytic cavity, correctly position the template 3' terminus, transfer the products out of the catalytic site and orchestrate the transition from initiation to elongation.

摘要

本综述总结了近期对病毒RNA依赖性RNA聚合酶(RdRPs)进行结构和功能研究所获得的综合见解,主要聚焦于RNA合成起始机制。传统上,RNA病毒的复制研究采用生物化学和遗传学方法相结合的方式。最近,已确定了六种病毒RdRPs的高分辨率结构。对于其中三种RdRPs,还解析了其与金属离子、单链RNA和/或核苷三磷酸形成的酶复合物结构。这些进展拓展了我们对病毒RNA合成分子机制的理解,并通过有针对性的定点诱变促进了对RdRPs的进一步研究。结果表明,基本的聚合酶右手形状为核苷酸转移催化的活性位点提供了底物分子和金属离子的正确几何排列,而不同系统中已进化出独特的结构元件以确保RNA合成的高效起始。这些元件将模板、核苷三磷酸和离子送入催化腔,正确定位模板3'末端,将产物从催化位点转移出去,并协调从起始到延伸的转变。

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