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靶向严重急性呼吸综合征冠状病毒2木瓜蛋白酶样蛋白酶的潜在抑制剂:一石二鸟。

Potential Inhibitors Targeting Papain-Like Protease of SARS-CoV-2: Two Birds With One Stone.

作者信息

Jiang Haihai, Yang Peiyao, Zhang Jin

机构信息

School of Basic Medical Sciences, Nanchang University, Nanchang, China.

Queen Mary School, Nanchang University, Nanchang, China.

出版信息

Front Chem. 2022 Feb 23;10:822785. doi: 10.3389/fchem.2022.822785. eCollection 2022.

Abstract

Severe acute respiratory syndrome Coronavirus-2 (SARS-CoV-2), the pathogen of the Coronavirus disease-19 (COVID-19), is still devastating the world causing significant chaos to the international community and posing a significant threat to global health. Since the first outbreak in late 2019, several lines of intervention have been developed to prevent the spread of this virus. Nowadays, some vaccines have been approved and extensively administered. However, the fact that SARS-CoV-2 rapidly mutates makes the efficacy and safety of this approach constantly under debate. Therefore, antivirals are still needed to combat the infection of SARS-CoV-2. Papain-like protease (PLpro) of SARS-CoV-2 supports viral reproduction and suppresses the innate immune response of the host, which makes PLpro an attractive pharmaceutical target. Inhibition of PLpro could not only prevent viral replication but also restore the antiviral immunity of the host, resulting in the speedy recovery of the patient. In this review, we describe structural and functional features on PLpro of SARS-CoV-2 and the latest development in searching for PLpro inhibitors. Currently available inhibitors targeting PLpro as well as their structural basis are also summarized.

摘要

严重急性呼吸综合征冠状病毒2(SARS-CoV-2)是冠状病毒病19(COVID-19)的病原体,仍在肆虐全球,给国际社会带来巨大混乱,并对全球健康构成重大威胁。自2019年末首次爆发以来,已开发出多种干预措施来防止这种病毒的传播。如今,一些疫苗已获批准并广泛接种。然而,SARS-CoV-2迅速变异这一事实使得这种方法的有效性和安全性一直备受争议。因此,仍需要抗病毒药物来对抗SARS-CoV-2感染。SARS-CoV-2的木瓜样蛋白酶(PLpro)支持病毒繁殖并抑制宿主的先天免疫反应,这使得PLpro成为一个有吸引力的药物靶点。抑制PLpro不仅可以阻止病毒复制,还可以恢复宿主的抗病毒免疫力,从而使患者迅速康复。在这篇综述中,我们描述了SARS-CoV-2的PLpro的结构和功能特征以及寻找PLpro抑制剂的最新进展。还总结了目前可用的靶向PLpro的抑制剂及其结构基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4796/8905519/93f8b6549b92/fchem-10-822785-g001.jpg

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