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Repurposing clinically approved drugs for COVID-19 treatment targeting SARS-CoV-2 papain-like protease
COVID-19 is a disease caused by SARS-CoV-2, which has led to more than 4 million deaths worldwide. As a result, there is a worldwide effort to develop specific drugs for targeting COVID-19. Papain-like protease (PLpro) is an attractive drug target because it has multiple essential functions involved...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8342870/ https://www.ncbi.nlm.nih.gov/pubmed/34364941 http://dx.doi.org/10.1016/j.ijbiomac.2021.07.184 |
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author | Xu, Yunxia Chen, Ke Pan, Juanli Lei, Yingshou Zhang, Danting Fang, Lipei Tang, Jinle Chen, Xin Ma, Yanhong Zheng, Yi Zhang, Bao Zhou, Yaoqi Zhan, Jian Xu, Wei |
author_facet | Xu, Yunxia Chen, Ke Pan, Juanli Lei, Yingshou Zhang, Danting Fang, Lipei Tang, Jinle Chen, Xin Ma, Yanhong Zheng, Yi Zhang, Bao Zhou, Yaoqi Zhan, Jian Xu, Wei |
author_sort | Xu, Yunxia |
collection | PubMed |
description | COVID-19 is a disease caused by SARS-CoV-2, which has led to more than 4 million deaths worldwide. As a result, there is a worldwide effort to develop specific drugs for targeting COVID-19. Papain-like protease (PLpro) is an attractive drug target because it has multiple essential functions involved in processing viral proteins, including viral genome replication and removal of post-translational ubiquitination modifications. Here, we established two assays for screening PLpro inhibitors according to protease and anti-ISGylation activities, respectively. Application of the two screening techniques to the library of clinically approved drugs led to the discovery of tanshinone IIA sulfonate sodium and chloroxine with their IC50 values of lower than 10 μM. These two compounds were found to directly interact with PLpro and their molecular mechanisms of binding were illustrated by docking and molecular dynamics simulations. The results highlight the usefulness of the two developed screening techniques for locating PLpro inhibitors. |
format | Online Article Text |
id | pubmed-8342870 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83428702021-08-06 Repurposing clinically approved drugs for COVID-19 treatment targeting SARS-CoV-2 papain-like protease Xu, Yunxia Chen, Ke Pan, Juanli Lei, Yingshou Zhang, Danting Fang, Lipei Tang, Jinle Chen, Xin Ma, Yanhong Zheng, Yi Zhang, Bao Zhou, Yaoqi Zhan, Jian Xu, Wei Int J Biol Macromol Article COVID-19 is a disease caused by SARS-CoV-2, which has led to more than 4 million deaths worldwide. As a result, there is a worldwide effort to develop specific drugs for targeting COVID-19. Papain-like protease (PLpro) is an attractive drug target because it has multiple essential functions involved in processing viral proteins, including viral genome replication and removal of post-translational ubiquitination modifications. Here, we established two assays for screening PLpro inhibitors according to protease and anti-ISGylation activities, respectively. Application of the two screening techniques to the library of clinically approved drugs led to the discovery of tanshinone IIA sulfonate sodium and chloroxine with their IC50 values of lower than 10 μM. These two compounds were found to directly interact with PLpro and their molecular mechanisms of binding were illustrated by docking and molecular dynamics simulations. The results highlight the usefulness of the two developed screening techniques for locating PLpro inhibitors. Elsevier B.V. 2021-10-01 2021-08-06 /pmc/articles/PMC8342870/ /pubmed/34364941 http://dx.doi.org/10.1016/j.ijbiomac.2021.07.184 Text en © 2021 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Xu, Yunxia Chen, Ke Pan, Juanli Lei, Yingshou Zhang, Danting Fang, Lipei Tang, Jinle Chen, Xin Ma, Yanhong Zheng, Yi Zhang, Bao Zhou, Yaoqi Zhan, Jian Xu, Wei Repurposing clinically approved drugs for COVID-19 treatment targeting SARS-CoV-2 papain-like protease |
title | Repurposing clinically approved drugs for COVID-19 treatment targeting SARS-CoV-2 papain-like protease |
title_full | Repurposing clinically approved drugs for COVID-19 treatment targeting SARS-CoV-2 papain-like protease |
title_fullStr | Repurposing clinically approved drugs for COVID-19 treatment targeting SARS-CoV-2 papain-like protease |
title_full_unstemmed | Repurposing clinically approved drugs for COVID-19 treatment targeting SARS-CoV-2 papain-like protease |
title_short | Repurposing clinically approved drugs for COVID-19 treatment targeting SARS-CoV-2 papain-like protease |
title_sort | repurposing clinically approved drugs for covid-19 treatment targeting sars-cov-2 papain-like protease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8342870/ https://www.ncbi.nlm.nih.gov/pubmed/34364941 http://dx.doi.org/10.1016/j.ijbiomac.2021.07.184 |
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