Vitamin C Binds to SARS Coronavirus-2 Main Protease Essential for Viral Replication

Author:

Malla Tek NarsinghORCID,Pandey SurajORCID,Aldama Luis,Feliz Dennisse,Noda MoraimaORCID,Poudyal IshworORCID,Phillips George N.ORCID,Stojković Emina A.ORCID,Schmidt MariusORCID

Abstract

AbstractThere is an urgent need for anti-viral agents that treat and/or prevent Covid-19 caused by SARS-Coronavirus (CoV-2) infections. The replication of the SARS CoV-2 is dependent on the activity of two cysteine proteases, a papain-like protease, PL-pro, and the 3C-like protease known as main protease Mpro or 3CLpro. The shortest and the safest path to clinical use is the repurposing of drugs with binding affinity to PLpro or 3CLpro that have an established safety profile in humans. Several studies have reported crystal structures of SARS-CoV-2 main protease in complex with FDA approved drugs such as those used in treatment of hepatitis C. Here, we report the crystal structure of 3CLpro in complex Vitamin C (L-ascorbate) bound to the protein’s active site at 2.5 Ångstrom resolution. The crystal structure of the Vitamin C 3CLpro complex may aid future studies on the effect of Vitamin C not only on the coronavirus main protease but on related proteases of other infectious viruses.

Publisher

Cold Spring Harbor Laboratory

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Repurposing of Chemotherapeutics to Combat COVID-19;Current Topics in Medicinal Chemistry;2022-12

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