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Emodin blocks the SARS coronavirus spike protein and angiotensin-converting enzyme 2 interaction
Severe acute respiratory syndrome (SARS) is an emerging infectious disease caused by a novel coronavirus (SARS-CoV). SARS-CoV spike (S) protein, a type I membrane-bound protein, is essential for the viral attachment to the host cell receptor angiotensin-converting enzyme 2 (ACE2). By screening 312 c...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114332/ https://www.ncbi.nlm.nih.gov/pubmed/16730806 http://dx.doi.org/10.1016/j.antiviral.2006.04.014 |
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author | Ho, Tin-Yun Wu, Shih-Lu Chen, Jaw-Chyun Li, Chia-Cheng Hsiang, Chien-Yun |
author_facet | Ho, Tin-Yun Wu, Shih-Lu Chen, Jaw-Chyun Li, Chia-Cheng Hsiang, Chien-Yun |
author_sort | Ho, Tin-Yun |
collection | PubMed |
description | Severe acute respiratory syndrome (SARS) is an emerging infectious disease caused by a novel coronavirus (SARS-CoV). SARS-CoV spike (S) protein, a type I membrane-bound protein, is essential for the viral attachment to the host cell receptor angiotensin-converting enzyme 2 (ACE2). By screening 312 controlled Chinese medicinal herbs supervised by Committee on Chinese Medicine and Pharmacy at Taiwan, we identified that three widely used Chinese medicinal herbs of the family Polygonaceae inhibited the interaction of SARS-CoV S protein and ACE2. The IC(50) values for Radix et Rhizoma Rhei (the root tubers of Rheum officinale Baill.), Radix Polygoni multiflori (the root tubers of Polygonum multiflorum Thunb.), and Caulis Polygoni multiflori (the vines of P. multiflorum Thunb.) ranged from 1 to 10 μg/ml. Emodin, an anthraquinone compound derived from genus Rheum and Polygonum, significantly blocked the S protein and ACE2 interaction in a dose-dependent manner. It also inhibited the infectivity of S protein-pseudotyped retrovirus to Vero E6 cells. These findings suggested that emodin may be considered as a potential lead therapeutic agent in the treatment of SARS. |
format | Online Article Text |
id | pubmed-7114332 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71143322020-04-02 Emodin blocks the SARS coronavirus spike protein and angiotensin-converting enzyme 2 interaction Ho, Tin-Yun Wu, Shih-Lu Chen, Jaw-Chyun Li, Chia-Cheng Hsiang, Chien-Yun Antiviral Res Article Severe acute respiratory syndrome (SARS) is an emerging infectious disease caused by a novel coronavirus (SARS-CoV). SARS-CoV spike (S) protein, a type I membrane-bound protein, is essential for the viral attachment to the host cell receptor angiotensin-converting enzyme 2 (ACE2). By screening 312 controlled Chinese medicinal herbs supervised by Committee on Chinese Medicine and Pharmacy at Taiwan, we identified that three widely used Chinese medicinal herbs of the family Polygonaceae inhibited the interaction of SARS-CoV S protein and ACE2. The IC(50) values for Radix et Rhizoma Rhei (the root tubers of Rheum officinale Baill.), Radix Polygoni multiflori (the root tubers of Polygonum multiflorum Thunb.), and Caulis Polygoni multiflori (the vines of P. multiflorum Thunb.) ranged from 1 to 10 μg/ml. Emodin, an anthraquinone compound derived from genus Rheum and Polygonum, significantly blocked the S protein and ACE2 interaction in a dose-dependent manner. It also inhibited the infectivity of S protein-pseudotyped retrovirus to Vero E6 cells. These findings suggested that emodin may be considered as a potential lead therapeutic agent in the treatment of SARS. Elsevier B.V. 2007-05 2006-05-15 /pmc/articles/PMC7114332/ /pubmed/16730806 http://dx.doi.org/10.1016/j.antiviral.2006.04.014 Text en Copyright © 2006 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 Ho, Tin-Yun Wu, Shih-Lu Chen, Jaw-Chyun Li, Chia-Cheng Hsiang, Chien-Yun Emodin blocks the SARS coronavirus spike protein and angiotensin-converting enzyme 2 interaction |
title | Emodin blocks the SARS coronavirus spike protein and angiotensin-converting enzyme 2 interaction |
title_full | Emodin blocks the SARS coronavirus spike protein and angiotensin-converting enzyme 2 interaction |
title_fullStr | Emodin blocks the SARS coronavirus spike protein and angiotensin-converting enzyme 2 interaction |
title_full_unstemmed | Emodin blocks the SARS coronavirus spike protein and angiotensin-converting enzyme 2 interaction |
title_short | Emodin blocks the SARS coronavirus spike protein and angiotensin-converting enzyme 2 interaction |
title_sort | emodin blocks the sars coronavirus spike protein and angiotensin-converting enzyme 2 interaction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114332/ https://www.ncbi.nlm.nih.gov/pubmed/16730806 http://dx.doi.org/10.1016/j.antiviral.2006.04.014 |
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