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Evaluation of RevX solution extract as a potential inhibitor of the main protease of SARS-CoV-2—In vitro study and molecular docking

The main protease (M(pro)) of SARS-CoV-2 is a protease necessary for viral polyprotein processing and maturation. M(pro) cleaves the polypeptide sequence after the glutamine residues. There is no known cellular protease with this substrate specificity in humans; therefore, it is considered an attrac...

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Autores principales: Chou, Feng-Pai, Liu, Chia-Chun, Huong Giang, Huynh Nguyet, Huang, Sheng-Cih, Hsu, Hsiu-Fu, Wu, Tung-Kung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8882484/
https://www.ncbi.nlm.nih.gov/pubmed/35252620
http://dx.doi.org/10.1016/j.heliyon.2022.e09034
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author Chou, Feng-Pai
Liu, Chia-Chun
Huong Giang, Huynh Nguyet
Huang, Sheng-Cih
Hsu, Hsiu-Fu
Wu, Tung-Kung
author_facet Chou, Feng-Pai
Liu, Chia-Chun
Huong Giang, Huynh Nguyet
Huang, Sheng-Cih
Hsu, Hsiu-Fu
Wu, Tung-Kung
author_sort Chou, Feng-Pai
collection PubMed
description The main protease (M(pro)) of SARS-CoV-2 is a protease necessary for viral polyprotein processing and maturation. M(pro) cleaves the polypeptide sequence after the glutamine residues. There is no known cellular protease with this substrate specificity in humans; therefore, it is considered an attractive drug target. Previously, fermented sorghum extract RevX (trademark of Revolutrx INC.) solution significantly alleviated physical decline and complications in a patient with lung adenocarcinoma, suggesting the role of bioactive components in RevX solution. To further explore whether the bioactive components in RevX solution exhibit other biological activities, such as antiviral effects, we investigated its inhibitory effect on the M(pro) of SARS-CoV-2 virus. We report herein that the solid extract of the RevX solution exhibits an efficacious M(pro) inhibitory activity, with IC(50) of 2.07 ± 0.38 μg/mL. Molecular docking of sterol-like components in the RevX extracts identified by MS shows that the three sterol-like molecules can bind to the active region of the GC376-M(pro) complex, supporting the structure-function relationship. Combined with its ability to significantly alleviate the body's immunity decline and to inhibit the activity of SARS-CoV-2 M(pro), RevX solution may provide a possible alternative supportive treatment for patients with COVID-19.
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spelling pubmed-88824842022-02-28 Evaluation of RevX solution extract as a potential inhibitor of the main protease of SARS-CoV-2—In vitro study and molecular docking Chou, Feng-Pai Liu, Chia-Chun Huong Giang, Huynh Nguyet Huang, Sheng-Cih Hsu, Hsiu-Fu Wu, Tung-Kung Heliyon Research Article The main protease (M(pro)) of SARS-CoV-2 is a protease necessary for viral polyprotein processing and maturation. M(pro) cleaves the polypeptide sequence after the glutamine residues. There is no known cellular protease with this substrate specificity in humans; therefore, it is considered an attractive drug target. Previously, fermented sorghum extract RevX (trademark of Revolutrx INC.) solution significantly alleviated physical decline and complications in a patient with lung adenocarcinoma, suggesting the role of bioactive components in RevX solution. To further explore whether the bioactive components in RevX solution exhibit other biological activities, such as antiviral effects, we investigated its inhibitory effect on the M(pro) of SARS-CoV-2 virus. We report herein that the solid extract of the RevX solution exhibits an efficacious M(pro) inhibitory activity, with IC(50) of 2.07 ± 0.38 μg/mL. Molecular docking of sterol-like components in the RevX extracts identified by MS shows that the three sterol-like molecules can bind to the active region of the GC376-M(pro) complex, supporting the structure-function relationship. Combined with its ability to significantly alleviate the body's immunity decline and to inhibit the activity of SARS-CoV-2 M(pro), RevX solution may provide a possible alternative supportive treatment for patients with COVID-19. Elsevier 2022-02-28 /pmc/articles/PMC8882484/ /pubmed/35252620 http://dx.doi.org/10.1016/j.heliyon.2022.e09034 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Chou, Feng-Pai
Liu, Chia-Chun
Huong Giang, Huynh Nguyet
Huang, Sheng-Cih
Hsu, Hsiu-Fu
Wu, Tung-Kung
Evaluation of RevX solution extract as a potential inhibitor of the main protease of SARS-CoV-2—In vitro study and molecular docking
title Evaluation of RevX solution extract as a potential inhibitor of the main protease of SARS-CoV-2—In vitro study and molecular docking
title_full Evaluation of RevX solution extract as a potential inhibitor of the main protease of SARS-CoV-2—In vitro study and molecular docking
title_fullStr Evaluation of RevX solution extract as a potential inhibitor of the main protease of SARS-CoV-2—In vitro study and molecular docking
title_full_unstemmed Evaluation of RevX solution extract as a potential inhibitor of the main protease of SARS-CoV-2—In vitro study and molecular docking
title_short Evaluation of RevX solution extract as a potential inhibitor of the main protease of SARS-CoV-2—In vitro study and molecular docking
title_sort evaluation of revx solution extract as a potential inhibitor of the main protease of sars-cov-2—in vitro study and molecular docking
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8882484/
https://www.ncbi.nlm.nih.gov/pubmed/35252620
http://dx.doi.org/10.1016/j.heliyon.2022.e09034
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