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针对 COVID-19 时代冠状病毒蛋白酶 nsp5(3CL,M)的新型结构和功能特征。

Targeting novel structural and functional features of coronavirus protease nsp5 (3CL, M) in the age of COVID-19.

机构信息

Department of Biological Sciences, Butler University, Indianapolis, IN, USA.

Department of Biology, DeSales University, Center Valley, PA, USA.

出版信息

J Gen Virol. 2021 Mar;102(3). doi: 10.1099/jgv.0.001558. Epub 2021 Jan 28.

Abstract

Coronavirus protease nsp5 (M, 3CL) remains a primary target for coronavirus therapeutics due to its indispensable and conserved role in the proteolytic processing of the viral replicase polyproteins. In this review, we discuss the diversity of known coronaviruses, the role of nsp5 in coronavirus biology, and the structure and function of this protease across the diversity of known coronaviruses, and evaluate past and present efforts to develop inhibitors to the nsp5 protease with a particular emphasis on new and mostly unexplored potential targets of inhibition. With the recent emergence of pandemic SARS-CoV-2, this review provides novel and potentially innovative strategies and directions to develop effective therapeutics against the coronavirus protease nsp5.

摘要

冠状病毒蛋白酶 nsp5(M,3CL)在病毒复制酶多蛋白的蛋白水解加工过程中具有不可或缺且保守的作用,因此仍然是冠状病毒治疗的主要靶点。在这篇综述中,我们讨论了已知冠状病毒的多样性、nsp5 在冠状病毒生物学中的作用,以及该蛋白酶在不同已知冠状病毒中的结构和功能,并评估了过去和现在开发 nsp5 蛋白酶抑制剂的努力,特别强调了新的和大多未被探索的抑制潜在靶点。随着最近大流行的 SARS-CoV-2 的出现,本综述为开发针对冠状病毒蛋白酶 nsp5 的有效治疗方法提供了新颖且具有潜在创新性的策略和方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c1/8515871/b9b528f8c83c/jgv-102-1558-g001.jpg

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