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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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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. |
format | Online Article Text |
id | pubmed-8882484 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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