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严重急性呼吸综合征冠状病毒2型主要蛋白酶(M):结构、功能及针对2019冠状病毒病的新兴疗法

The SARS-CoV-2 main protease (M): Structure, function, and emerging therapies for COVID-19.

作者信息

Hu Qing, Xiong Yuan, Zhu Guang-Hao, Zhang Ya-Ni, Zhang Yi-Wen, Huang Ping, Ge Guang-Bo

机构信息

Shanghai Frontiers Science Center of TCM Chemical Biology Institute of Interdisciplinary Integrative Medicine Research Shanghai University of Traditional Chinese Medicine Shanghai China.

Clinical Pharmacy Center Cancer Center Department of Pharmacy Zhejiang Provincial People's Hospital Affiliated People's Hospital Hangzhou Medical College, Hangzhou Zhejiang China.

出版信息

MedComm (2020). 2022 Jul 14;3(3):e151. doi: 10.1002/mco2.151. eCollection 2022 Sep.

Abstract

The main proteases (M), also termed 3-chymotrypsin-like proteases (3CL), are a class of highly conserved cysteine hydrolases in β-coronaviruses. Increasing evidence has demonstrated that 3CLs play an indispensable role in viral replication and have been recognized as key targets for preventing and treating coronavirus-caused infectious diseases, including COVID-19. This review is focused on the structural features and biological function of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) main protease M (also known as 3CL), as well as recent advances in discovering and developing SARS-CoV-2 3CL inhibitors. To better understand the characteristics of SARS-CoV-2 3CL inhibitors, the inhibition activities, inhibitory mechanisms, and key structural features of various 3CL inhibitors (including marketed drugs, peptidomimetic, and non-peptidomimetic synthetic compounds, as well as natural compounds and their derivatives) are summarized comprehensively. Meanwhile, the challenges in this field are highlighted, while future directions for designing and developing efficacious 3CL inhibitors as novel anti-coronavirus therapies are also proposed. Collectively, all information and knowledge presented here are very helpful for understanding the structural features and inhibitory mechanisms of SARS-CoV-2 3CL inhibitors, which offers new insights or inspiration to medicinal chemists for designing and developing more efficacious 3CL inhibitors as novel anti-coronavirus agents.

摘要

主要蛋白酶(M),也称为3-糜蛋白酶样蛋白酶(3CL),是β冠状病毒中一类高度保守的半胱氨酸水解酶。越来越多的证据表明,3CL在病毒复制中起着不可或缺的作用,并已被公认为预防和治疗包括COVID-19在内的冠状病毒引起的传染病的关键靶点。本综述聚焦于严重急性呼吸综合征冠状病毒2(SARS-CoV-2)主要蛋白酶M(也称为3CL)的结构特征和生物学功能,以及SARS-CoV-2 3CL抑制剂发现和开发的最新进展。为了更好地了解SARS-CoV-2 3CL抑制剂的特性,全面总结了各种3CL抑制剂(包括上市药物、拟肽和非拟肽合成化合物以及天然化合物及其衍生物)的抑制活性、抑制机制和关键结构特征。同时,强调了该领域的挑战,还提出了设计和开发有效的3CL抑制剂作为新型抗冠状病毒疗法的未来方向。总体而言,这里呈现的所有信息和知识对于理解SARS-CoV-2 3CL抑制剂的结构特征和抑制机制非常有帮助,为药物化学家设计和开发更有效的3CL抑制剂作为新型抗冠状病毒药物提供了新的见解或灵感。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7775/9283855/08e7671639fb/MCO2-3-e151-g007.jpg

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