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冠状病毒进入机制:我们如何了解到 SARS-CoV-2。

Coronavirus entry: how we arrived at SARS-CoV-2.

机构信息

Department of Microbiology and Immunology and Master of Public Health Program, Cornell University, Ithaca, NY, USA.

Robert Frederick Smith School of Chemical & Biomolecular Engineering, Cornell University, Ithaca, NY, USA.

出版信息

Curr Opin Virol. 2021 Apr;47:113-120. doi: 10.1016/j.coviro.2021.02.006. Epub 2021 Mar 9.

Abstract

Because of the COVID-19 pandemic, the novel coronavirus SARS-CoV-2 has risen to shape scientific research during 2020, with its spike (S) protein being a predominant focus. The S protein is likely the most complicated of all viral glycoproteins and is a key factor in immunological responses and virus pathogenesis. It is also the driving force dictating virus entry mechanisms, which are highly 'plastic' for coronaviruses, allowing a plethora of options for different virus variants and strains in different cell types. Here we review coronavirus entry as a foundation for current work on SARS-CoV-2. We focus on the post-receptor binding events and cellular pathways that direct the membrane fusion events necessary for genome delivery, including S proteolytic priming and activation. We also address aspects of the entry process important for virus evolution and therapeutic development.

摘要

由于 COVID-19 大流行,新型冠状病毒 SARS-CoV-2 在 2020 年成为科学研究的热点,其刺突(S)蛋白是主要关注点。S 蛋白可能是所有病毒糖蛋白中最复杂的,也是免疫反应和病毒发病机制的关键因素。它也是决定病毒进入机制的驱动力,冠状病毒的进入机制具有高度的“可塑性”,允许不同病毒变体和不同细胞类型中的不同毒株有多种选择。在这里,我们回顾冠状病毒进入作为当前 SARS-CoV-2 工作的基础。我们专注于受体结合后事件和细胞途径,这些途径指导基因组传递所必需的膜融合事件,包括 S 蛋白的蛋白水解引发和激活。我们还讨论了对病毒进化和治疗开发很重要的进入过程的各个方面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a11d/7942143/b9126a213b83/gr1_lrg.jpg

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