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病毒用于对接和递送至核孔复合体的机制。

Viral mechanisms for docking and delivering at nuclear pore complexes.

机构信息

Department of Molecular Life Sciences, University of Zurich, Winterthurerstrasse 190, 8057 Zurich, Switzerland.

出版信息

Semin Cell Dev Biol. 2017 Aug;68:59-71. doi: 10.1016/j.semcdb.2017.05.008. Epub 2017 May 12.

Abstract

Some viruses possess the remarkable ability to transport their genomes across nuclear pore complexes (NPCs) for replication inside the host cell's intact nuclear compartment. Viral mechanisms for crossing the restrictive NPC passageway are highly complex and astonishingly diverse, requiring in each case stepwise interaction between incoming virus particles and components of the nuclear transport machinery. Exactly how a large viral genome loaded with accessory proteins is able to pass through the relatively narrow central channel of the NPC without causing catastrophic structural damage is not yet fully understood. It appears likely, however, that the overall structure of the NPC changes in response to the cargo. Translocation may result in nucleic acids being misdelivered to the cytoplasm. Here we consider in detail the diverse strategies that viruses have evolved to target and subvert NPCs during infection. For decades, this process has both captivated and confounded researchers in the fields of virology, cell biology, and structural biology.

摘要

有些病毒具有将其基因组穿过核孔复合体 (NPC) 运输到宿主细胞完整核区进行复制的惊人能力。病毒穿越限制 NPC 通道的机制非常复杂,令人惊讶的多样化,每种情况都需要传入病毒颗粒与核运输机制成分之间逐步相互作用。目前还不完全清楚,载有辅助蛋白的大型病毒基因组如何能够在不引起灾难性结构损伤的情况下通过 NPC 相对较窄的中央通道。然而,似乎 NPC 的整体结构会对货物做出响应而发生改变。易位可能导致核酸被错误递送到细胞质中。在这里,我们详细讨论了病毒在感染过程中针对和颠覆 NPC 所采用的多种策略。几十年来,这个过程一直吸引着病毒学、细胞生物学和结构生物学领域的研究人员,并使他们感到困惑。

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