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原子分辨率捕获的微小核糖核酸病毒脱壳中间产物。

Picornavirus uncoating intermediate captured in atomic detail.

机构信息

Division of Structural Biology, University of Oxford, Headington, Oxford, UK.

出版信息

Nat Commun. 2013;4:1929. doi: 10.1038/ncomms2889.

Abstract

It remains largely mysterious how the genomes of non-enveloped eukaryotic viruses are transferred across a membrane into the host cell. Picornaviruses are simple models for such viruses, and initiate this uncoating process through particle expansion, which reveals channels through which internal capsid proteins and the viral genome presumably exit the particle, although this has not been clearly seen until now. Here we present the atomic structure of an uncoating intermediate for the major human picornavirus pathogen CAV16, which reveals VP1 partly extruded from the capsid, poised to embed in the host membrane. Together with previous low-resolution results, we are able to propose a detailed hypothesis for the ordered egress of the internal proteins, using two distinct sets of channels through the capsid, and suggest a structural link to the condensed RNA within the particle, which may be involved in triggering RNA release.

摘要

包膜型真核病毒的基因组如何通过细胞膜进入宿主细胞,这在很大程度上仍是未解之谜。小核糖核酸病毒是此类病毒的简单模型,它们通过粒子膨胀启动脱壳过程,这揭示了内部衣壳蛋白和病毒基因组可能离开粒子的通道,尽管直到现在还没有清楚地看到这一点。在这里,我们展示了主要人类小核糖核酸病毒病原体 CAV16 的一个脱壳中间产物的原子结构,该结构显示 VP1 部分从衣壳中伸出,准备嵌入宿主膜中。结合以前的低分辨率结果,我们能够使用衣壳中的两组不同的通道,提出一个关于内部蛋白有序排出的详细假设,并提出与粒子内浓缩 RNA 的结构联系,这可能与触发 RNA 释放有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/916b/3709478/c0be10c11f17/ncomms2889-f1.jpg

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