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Mechanism of enterovirus VP0 maturation cleavage based on the structure of a stabilised assembly intermediate

机译:基于稳定组装中间体结构的肠道病毒VP0成熟裂解机制

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摘要

Molecular details of genome packaging are little understood for the majority of viruses. In enteroviruses (EVs), cleavage of the structural protein VP0 into VP4 and VP2 is initiated by the incorporation of RNA into the assembling virion and is essential for infectivity. We have applied a combination of bioinformatic, molecular and structural approaches to generate the first high-resolution structure of an intermediate in the assembly pathway, termed a provirion, which contains RNA and intact VP0. We have demonstrated an essential role of VP0 E096 in VP0 cleavage independent of RNA encapsidation and generated a new model of capsid maturation, supported by bioinformatic analysis. This provides a molecular basis for RNA-dependence, where RNA induces conformational changes required for VP0 maturation, but that RNA packaging itself is not sufficient to induce maturation. These data have implications for understanding production of infectious virions and potential relevance for future vaccine and antiviral drug design.
机译:对于大多数病毒,基因组包装的分子细节知之甚少。在肠道病毒 (EV) 中,结构蛋白 VP0 裂解成 VP4 和 VP2 是通过将 RNA 掺入组装病毒粒子而启动的,并且对于传染性至关重要。我们应用了生物信息学、分子和结构方法的组合,在组装途径中生成了第一个高分辨率的中间体结构,称为 provirion,其中包含 RNA 和完整的 VP0。我们已经证明了 VP0 E096 在 VP0 切割中独立于 RNA 包封的重要作用,并在生物信息学分析的支持下生成了衣壳成熟的新模型。这为 RNA 依赖性提供了分子基础,其中 RNA 诱导 VP0 成熟所需的构象变化,但 RNA 包装本身不足以诱导成熟。这些数据对理解感染性病毒粒子的产生以及与未来疫苗和抗病毒药物设计的潜在相关性具有重要意义。
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