Cargando…

The inhibition of Mpro, the primary protease of COVID-19, by Poria cocos and its active compounds: a network pharmacology and molecular docking study

Poria cocos is a traditional Chinese medicine (TCM) that can clear dampness, promote diuresis, and strengthen the spleen and stomach. Poria cocos has been detected in many TCM compounds that are used for COVID-19 intervention. However, the active ingredients and mechanisms associated with the effect...

Descripción completa

Detalles Bibliográficos
Autores principales: Wu, Zhimin, Chen, Xiaoxue, Ni, Weiju, Zhou, Danshui, Chai, Shanshan, Ye, Weile, Zhang, Zhengpu, Guo, Yuanqiang, Ren, Liping, Zeng, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8696653/
https://www.ncbi.nlm.nih.gov/pubmed/35423770
http://dx.doi.org/10.1039/d0ra07035a
_version_ 1784619864862752768
author Wu, Zhimin
Chen, Xiaoxue
Ni, Weiju
Zhou, Danshui
Chai, Shanshan
Ye, Weile
Zhang, Zhengpu
Guo, Yuanqiang
Ren, Liping
Zeng, Yu
author_facet Wu, Zhimin
Chen, Xiaoxue
Ni, Weiju
Zhou, Danshui
Chai, Shanshan
Ye, Weile
Zhang, Zhengpu
Guo, Yuanqiang
Ren, Liping
Zeng, Yu
author_sort Wu, Zhimin
collection PubMed
description Poria cocos is a traditional Chinese medicine (TCM) that can clear dampness, promote diuresis, and strengthen the spleen and stomach. Poria cocos has been detected in many TCM compounds that are used for COVID-19 intervention. However, the active ingredients and mechanisms associated with the effect of Poria cocos on COVID-19 remain unclear. In this paper, the active ingredients of Poria cocos, along with their potential targets related to COVID-19, were screened using TCMSP, GeneCards, and other databases, by means of network pharmacology. We then investigated the active components, potential targets, and interactions, that are associated with COVID-19 intervention. The primary protease of COVID-19, Mpro, is currently a key target in the design of potential inhibitors. Molecular docking techniques and molecular dynamics simulations demonstrated that the active components of Poria cocos could bind stably to the active site of Mpro with high levels of binding activity. Pachymic acid is based on a triterpene structure and was identified as the main component of Poria cocos; its triterpene active component has low binding energy with Mpro. The pachymic acid of Mpro activity was further characterized and the IC(50) was determined to be 18.607 μmol L(−1). Our results indicate that pachymic acid exhibits a certain inhibitory effect on the Mpro protease.
format Online
Article
Text
id pubmed-8696653
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher The Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-86966532022-04-13 The inhibition of Mpro, the primary protease of COVID-19, by Poria cocos and its active compounds: a network pharmacology and molecular docking study Wu, Zhimin Chen, Xiaoxue Ni, Weiju Zhou, Danshui Chai, Shanshan Ye, Weile Zhang, Zhengpu Guo, Yuanqiang Ren, Liping Zeng, Yu RSC Adv Chemistry Poria cocos is a traditional Chinese medicine (TCM) that can clear dampness, promote diuresis, and strengthen the spleen and stomach. Poria cocos has been detected in many TCM compounds that are used for COVID-19 intervention. However, the active ingredients and mechanisms associated with the effect of Poria cocos on COVID-19 remain unclear. In this paper, the active ingredients of Poria cocos, along with their potential targets related to COVID-19, were screened using TCMSP, GeneCards, and other databases, by means of network pharmacology. We then investigated the active components, potential targets, and interactions, that are associated with COVID-19 intervention. The primary protease of COVID-19, Mpro, is currently a key target in the design of potential inhibitors. Molecular docking techniques and molecular dynamics simulations demonstrated that the active components of Poria cocos could bind stably to the active site of Mpro with high levels of binding activity. Pachymic acid is based on a triterpene structure and was identified as the main component of Poria cocos; its triterpene active component has low binding energy with Mpro. The pachymic acid of Mpro activity was further characterized and the IC(50) was determined to be 18.607 μmol L(−1). Our results indicate that pachymic acid exhibits a certain inhibitory effect on the Mpro protease. The Royal Society of Chemistry 2021-03-25 /pmc/articles/PMC8696653/ /pubmed/35423770 http://dx.doi.org/10.1039/d0ra07035a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Wu, Zhimin
Chen, Xiaoxue
Ni, Weiju
Zhou, Danshui
Chai, Shanshan
Ye, Weile
Zhang, Zhengpu
Guo, Yuanqiang
Ren, Liping
Zeng, Yu
The inhibition of Mpro, the primary protease of COVID-19, by Poria cocos and its active compounds: a network pharmacology and molecular docking study
title The inhibition of Mpro, the primary protease of COVID-19, by Poria cocos and its active compounds: a network pharmacology and molecular docking study
title_full The inhibition of Mpro, the primary protease of COVID-19, by Poria cocos and its active compounds: a network pharmacology and molecular docking study
title_fullStr The inhibition of Mpro, the primary protease of COVID-19, by Poria cocos and its active compounds: a network pharmacology and molecular docking study
title_full_unstemmed The inhibition of Mpro, the primary protease of COVID-19, by Poria cocos and its active compounds: a network pharmacology and molecular docking study
title_short The inhibition of Mpro, the primary protease of COVID-19, by Poria cocos and its active compounds: a network pharmacology and molecular docking study
title_sort inhibition of mpro, the primary protease of covid-19, by poria cocos and its active compounds: a network pharmacology and molecular docking study
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8696653/
https://www.ncbi.nlm.nih.gov/pubmed/35423770
http://dx.doi.org/10.1039/d0ra07035a
work_keys_str_mv AT wuzhimin theinhibitionofmprotheprimaryproteaseofcovid19byporiacocosanditsactivecompoundsanetworkpharmacologyandmoleculardockingstudy
AT chenxiaoxue theinhibitionofmprotheprimaryproteaseofcovid19byporiacocosanditsactivecompoundsanetworkpharmacologyandmoleculardockingstudy
AT niweiju theinhibitionofmprotheprimaryproteaseofcovid19byporiacocosanditsactivecompoundsanetworkpharmacologyandmoleculardockingstudy
AT zhoudanshui theinhibitionofmprotheprimaryproteaseofcovid19byporiacocosanditsactivecompoundsanetworkpharmacologyandmoleculardockingstudy
AT chaishanshan theinhibitionofmprotheprimaryproteaseofcovid19byporiacocosanditsactivecompoundsanetworkpharmacologyandmoleculardockingstudy
AT yeweile theinhibitionofmprotheprimaryproteaseofcovid19byporiacocosanditsactivecompoundsanetworkpharmacologyandmoleculardockingstudy
AT zhangzhengpu theinhibitionofmprotheprimaryproteaseofcovid19byporiacocosanditsactivecompoundsanetworkpharmacologyandmoleculardockingstudy
AT guoyuanqiang theinhibitionofmprotheprimaryproteaseofcovid19byporiacocosanditsactivecompoundsanetworkpharmacologyandmoleculardockingstudy
AT renliping theinhibitionofmprotheprimaryproteaseofcovid19byporiacocosanditsactivecompoundsanetworkpharmacologyandmoleculardockingstudy
AT zengyu theinhibitionofmprotheprimaryproteaseofcovid19byporiacocosanditsactivecompoundsanetworkpharmacologyandmoleculardockingstudy
AT wuzhimin inhibitionofmprotheprimaryproteaseofcovid19byporiacocosanditsactivecompoundsanetworkpharmacologyandmoleculardockingstudy
AT chenxiaoxue inhibitionofmprotheprimaryproteaseofcovid19byporiacocosanditsactivecompoundsanetworkpharmacologyandmoleculardockingstudy
AT niweiju inhibitionofmprotheprimaryproteaseofcovid19byporiacocosanditsactivecompoundsanetworkpharmacologyandmoleculardockingstudy
AT zhoudanshui inhibitionofmprotheprimaryproteaseofcovid19byporiacocosanditsactivecompoundsanetworkpharmacologyandmoleculardockingstudy
AT chaishanshan inhibitionofmprotheprimaryproteaseofcovid19byporiacocosanditsactivecompoundsanetworkpharmacologyandmoleculardockingstudy
AT yeweile inhibitionofmprotheprimaryproteaseofcovid19byporiacocosanditsactivecompoundsanetworkpharmacologyandmoleculardockingstudy
AT zhangzhengpu inhibitionofmprotheprimaryproteaseofcovid19byporiacocosanditsactivecompoundsanetworkpharmacologyandmoleculardockingstudy
AT guoyuanqiang inhibitionofmprotheprimaryproteaseofcovid19byporiacocosanditsactivecompoundsanetworkpharmacologyandmoleculardockingstudy
AT renliping inhibitionofmprotheprimaryproteaseofcovid19byporiacocosanditsactivecompoundsanetworkpharmacologyandmoleculardockingstudy
AT zengyu inhibitionofmprotheprimaryproteaseofcovid19byporiacocosanditsactivecompoundsanetworkpharmacologyandmoleculardockingstudy