Suppr超能文献

靶向 SARS-CoV-2 主蛋白酶 M 的别构口袋。

Targeting allosteric pockets of SARS-CoV-2 main protease M.

机构信息

Multidisciplinary Centre for Advanced Research and Studies, Jamia Millia Islamia, New Delhi, India.

Department of Applied Sciences, Indian Institute of Information Technology, Allahabad, Allahabad, Uttar Pradesh, India.

出版信息

J Biomol Struct Dyn. 2022 Sep;40(14):6603-6618. doi: 10.1080/07391102.2021.1891141. Epub 2021 Feb 27.

Abstract

Repurposing of antivirals is an attractive therapeutic option for the treatment of COVID-19. Main protease (M, also called 3 C-like protease (3CL) is a key protease of SARS-CoV-2 involved in viral replication, and is a promising drug target for antivirals. A major challenge to test the efficacy of antivirals is the conformational plasticity of M and its future mutation prone flexibility. Suitable choice of drugs in catalytic and allosteric pockets appear to be essential for combination therapy. Current study, based on docking and extensive set of MD simulations, finds the combination of Elbasvir, Glecaprevir and Ritonavir to be a viable candidate for further experimental drug testing/pharmacophore design for M.Communicated by Ramaswamy H. Sarma.

摘要

重新利用抗病毒药物是治疗 COVID-19 的一种有吸引力的治疗选择。主蛋白酶 (M,也称为 3CL 样蛋白酶 (3CL)) 是 SARS-CoV-2 中参与病毒复制的关键蛋白酶,也是抗病毒药物的有前途的药物靶点。测试抗病毒药物疗效的主要挑战是 M 的构象灵活性及其未来易突变的灵活性。催化口袋和变构口袋中合适的药物选择似乎对联合治疗至关重要。本研究基于对接和广泛的 MD 模拟,发现 Elbasvir、Glecaprevir 和 Ritonavir 的组合是进一步进行实验药物测试/药效团设计的可行候选药物。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验