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微小核糖核酸病毒的RNA依赖RNA聚合酶:从结构到调控机制

RNA-Dependent RNA Polymerases of Picornaviruses: From the Structure to Regulatory Mechanisms.

作者信息

Ferrer-Orta Cristina, Ferrero Diego, Verdaguer Núria

机构信息

Molecular Biology Institute of Barcelona (CSIC), Barcelona Science Park (PCB), Baldiri i Reixac 10, Barcelona E-08028, Spain.

出版信息

Viruses. 2015 Aug 6;7(8):4438-60. doi: 10.3390/v7082829.

Abstract

RNA viruses typically encode their own RNA-dependent RNA polymerase (RdRP) to ensure genome replication within the infected cells. RdRP function is critical not only for the virus life cycle but also for its adaptive potential. The combination of low fidelity of replication and the absence of proofreading and excision activities within the RdRPs result in high mutation frequencies that allow these viruses a rapid adaptation to changing environments. In this review, we summarize the current knowledge about structural and functional aspects on RdRP catalytic complexes, focused mainly in the Picornaviridae family. The structural data currently available from these viruses provided high-resolution snapshots for a range of conformational states associated to RNA template-primer binding, rNTP recognition, catalysis and chain translocation. As these enzymes are major targets for the development of antiviral compounds, such structural information is essential for the design of new therapies.

摘要

RNA病毒通常编码自身的RNA依赖性RNA聚合酶(RdRP),以确保在受感染细胞内进行基因组复制。RdRP的功能不仅对病毒生命周期至关重要,对其适应潜力也很关键。复制的低保真性以及RdRP缺乏校对和切除活性,导致高突变频率,使这些病毒能够快速适应不断变化的环境。在本综述中,我们总结了目前关于RdRP催化复合物结构和功能方面的知识,主要聚焦于小RNA病毒科。目前从这些病毒获得的结构数据为一系列与RNA模板-引物结合、rNTP识别、催化和链转位相关的构象状态提供了高分辨率快照。由于这些酶是抗病毒化合物开发的主要靶点,此类结构信息对于新疗法的设计至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5723/4576190/566397657a1c/viruses-07-02829-g001a.jpg

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