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甲型流感病毒核糖核蛋白复合体在RNA合成过程中的构象动力学

Conformational Dynamics of Influenza A Virus Ribonucleoprotein Complexes during RNA Synthesis.

作者信息

Carlero Diego, Fukuda Shingo, Bocanegra Rebeca, Ando Toshio, Martin-Benito Jaime, Ibarra Borja

机构信息

Centro Nacional de Biotecnología Campus de Cantoblanco, 28049, Madrid, Spain.

WPI Nano Life Science Institute (WPI-NanoLSI), Kanazawa University, Kakuma-machi, Kanazawa 920-1192, Japan.

出版信息

ACS Nano. 2024 Jul 16;18(30):19518-27. doi: 10.1021/acsnano.4c01362.

Abstract

Viral ribonucleoproteins (vRNPs) are the cornerstones of viral proliferation, as they form the macromolecular complexes that are responsible for the transcription and replication of most single-stranded RNA viruses. The influenza A virus (IAV) polymerase catalyzes RNA synthesis within the context of vRNPs where genomic viral RNA (vRNA) is packaged by the viral nucleoprotein (NP). We used high-speed atomic force microscopy and electron microscopy to study the conformational dynamics of individual IAV recombinant RNPs (rRNPs) during RNA synthesis. The rRNPs present an annular organization that allows for the real-time tracking of conformational changes in the NP-vRNA template caused by the advancing polymerase. We demonstrate that the rRNPs undergo a well-defined conformational cycle during RNA synthesis, which can be interpreted in light of previous transcription models. We also present initial estimations of the average RNA synthesis rate in the rRNP and its dependence on the nucleotide concentration and stability of the nascent RNA secondary structures. Furthermore, we provide evidence that rRNPs can perform consecutive cycles of RNA synthesis, accounting for their ability to recycle and generate multiple copies of RNA.

摘要

病毒核糖核蛋白(vRNPs)是病毒增殖的基石,因为它们形成了负责大多数单链RNA病毒转录和复制的大分子复合物。甲型流感病毒(IAV)聚合酶在vRNPs的环境中催化RNA合成,其中基因组病毒RNA(vRNA)由病毒核蛋白(NP)包装。我们使用高速原子力显微镜和电子显微镜来研究RNA合成过程中单个IAV重组核糖核蛋白(rRNPs)的构象动力学。rRNPs呈现出一种环形结构,能够实时追踪由前进的聚合酶引起的NP-vRNA模板中的构象变化。我们证明,rRNPs在RNA合成过程中经历了一个明确的构象循环,这可以根据先前的转录模型来解释。我们还给出了rRNP中平均RNA合成速率的初步估计,以及它对核苷酸浓度和新生RNA二级结构稳定性的依赖性。此外,我们提供证据表明rRNPs可以进行连续的RNA合成循环,这解释了它们能够循环利用并产生多个RNA拷贝的能力。

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