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Potential inhibitor for blocking binding between ACE2 and SARS-CoV-2 spike protein with mutations

At the time of writing, more than 440 million confirmed coronavirus disease 2019 (COVID-19) cases and more than 5.97 million COVID-19 deaths worldwide have been reported by the World Health Organization since the start of the outbreak of the pandemic in Wuhan, China. During the COVID-19 pandemic, ma...

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Autores principales: Tsai, Ming-Shao, Shih, Wei-Tai, Yang, Yao-Hsu, Lin, Yu-Shih, Chang, Geng-He, Hsu, Cheng-Ming, Yeh, Reming-Albert, Shu, Li-Hsin, Cheng, Yu-Ching, Liu, Hung-Te, Wu, Yu-Huei, Wu, Yu-Heng, Shen, Rou-Chen, Wu, Ching-Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Authors. Published by Elsevier Masson SAS. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8906167/
https://www.ncbi.nlm.nih.gov/pubmed/35279013
http://dx.doi.org/10.1016/j.biopha.2022.112802
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author Tsai, Ming-Shao
Shih, Wei-Tai
Yang, Yao-Hsu
Lin, Yu-Shih
Chang, Geng-He
Hsu, Cheng-Ming
Yeh, Reming-Albert
Shu, Li-Hsin
Cheng, Yu-Ching
Liu, Hung-Te
Wu, Yu-Huei
Wu, Yu-Heng
Shen, Rou-Chen
Wu, Ching-Yuan
author_facet Tsai, Ming-Shao
Shih, Wei-Tai
Yang, Yao-Hsu
Lin, Yu-Shih
Chang, Geng-He
Hsu, Cheng-Ming
Yeh, Reming-Albert
Shu, Li-Hsin
Cheng, Yu-Ching
Liu, Hung-Te
Wu, Yu-Huei
Wu, Yu-Heng
Shen, Rou-Chen
Wu, Ching-Yuan
author_sort Tsai, Ming-Shao
collection PubMed
description At the time of writing, more than 440 million confirmed coronavirus disease 2019 (COVID-19) cases and more than 5.97 million COVID-19 deaths worldwide have been reported by the World Health Organization since the start of the outbreak of the pandemic in Wuhan, China. During the COVID-19 pandemic, many variants of SARS-CoV-2 have arisen because of high mutation rates. N501Y, E484K, K417N, K417T, L452R and T478K in the receptor binding domain (RBD) region may increase the infectivity in several variants of SARS-CoV-2. In this study, we discovered that GB-1, developed from Chiehyuan herbal formula which obtained from Tian Shang Sheng Mu of Chiayi Puzi Peitian Temple, can inhibit the binding between ACE2 and RBD with Wuhan type, K417N-E484K-N501Y and L452R-T478K mutation. In addition, GB-1 inhibited the binding between ACE2 and RBD with a single mutation (E484K or N501Y), except the K417N mutation. In the compositions of GB-1, glycyrrhizic acid can inhibit the binding between ACE2 and RBD with Wuhan type, except K417N-E484K-N501Y mutation. Our results suggest that GB-1 could be a potential candidate for the prophylaxis of different variants of SARS-CoV-2 infection because of its inhibition of binding between ACE2 and RBD with different mutations (L452R-T478K, K417N-E484K-N501Y, N501Y or E484K).
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spelling pubmed-89061672022-03-09 Potential inhibitor for blocking binding between ACE2 and SARS-CoV-2 spike protein with mutations Tsai, Ming-Shao Shih, Wei-Tai Yang, Yao-Hsu Lin, Yu-Shih Chang, Geng-He Hsu, Cheng-Ming Yeh, Reming-Albert Shu, Li-Hsin Cheng, Yu-Ching Liu, Hung-Te Wu, Yu-Huei Wu, Yu-Heng Shen, Rou-Chen Wu, Ching-Yuan Biomed Pharmacother Article At the time of writing, more than 440 million confirmed coronavirus disease 2019 (COVID-19) cases and more than 5.97 million COVID-19 deaths worldwide have been reported by the World Health Organization since the start of the outbreak of the pandemic in Wuhan, China. During the COVID-19 pandemic, many variants of SARS-CoV-2 have arisen because of high mutation rates. N501Y, E484K, K417N, K417T, L452R and T478K in the receptor binding domain (RBD) region may increase the infectivity in several variants of SARS-CoV-2. In this study, we discovered that GB-1, developed from Chiehyuan herbal formula which obtained from Tian Shang Sheng Mu of Chiayi Puzi Peitian Temple, can inhibit the binding between ACE2 and RBD with Wuhan type, K417N-E484K-N501Y and L452R-T478K mutation. In addition, GB-1 inhibited the binding between ACE2 and RBD with a single mutation (E484K or N501Y), except the K417N mutation. In the compositions of GB-1, glycyrrhizic acid can inhibit the binding between ACE2 and RBD with Wuhan type, except K417N-E484K-N501Y mutation. Our results suggest that GB-1 could be a potential candidate for the prophylaxis of different variants of SARS-CoV-2 infection because of its inhibition of binding between ACE2 and RBD with different mutations (L452R-T478K, K417N-E484K-N501Y, N501Y or E484K). The Authors. Published by Elsevier Masson SAS. 2022-05 2022-03-09 /pmc/articles/PMC8906167/ /pubmed/35279013 http://dx.doi.org/10.1016/j.biopha.2022.112802 Text en © 2022 The Authors 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
Tsai, Ming-Shao
Shih, Wei-Tai
Yang, Yao-Hsu
Lin, Yu-Shih
Chang, Geng-He
Hsu, Cheng-Ming
Yeh, Reming-Albert
Shu, Li-Hsin
Cheng, Yu-Ching
Liu, Hung-Te
Wu, Yu-Huei
Wu, Yu-Heng
Shen, Rou-Chen
Wu, Ching-Yuan
Potential inhibitor for blocking binding between ACE2 and SARS-CoV-2 spike protein with mutations
title Potential inhibitor for blocking binding between ACE2 and SARS-CoV-2 spike protein with mutations
title_full Potential inhibitor for blocking binding between ACE2 and SARS-CoV-2 spike protein with mutations
title_fullStr Potential inhibitor for blocking binding between ACE2 and SARS-CoV-2 spike protein with mutations
title_full_unstemmed Potential inhibitor for blocking binding between ACE2 and SARS-CoV-2 spike protein with mutations
title_short Potential inhibitor for blocking binding between ACE2 and SARS-CoV-2 spike protein with mutations
title_sort potential inhibitor for blocking binding between ace2 and sars-cov-2 spike protein with mutations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8906167/
https://www.ncbi.nlm.nih.gov/pubmed/35279013
http://dx.doi.org/10.1016/j.biopha.2022.112802
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