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Dexamethasone inhibits SARS-CoV-2 spike pseudotyped virus viropexis by binding to ACE2
The SARS-CoV-2 outbreak, began in late 2019, has caused a worldwide pandemic and shows no signs of slowing. Glucocorticoids (GCs), including dexamethasone (DEX), have been widely used as effective anti-inflammatory and immunosuppressant drugs. In this study, seven GCs had no obvious effect on cell v...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7744032/ https://www.ncbi.nlm.nih.gov/pubmed/33387788 http://dx.doi.org/10.1016/j.virol.2020.12.001 |
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author | Zhang, Yongjing Hu, Shiling Wang, Jue Xue, Zhuoyin Wang, Cheng Wang, Nan |
author_facet | Zhang, Yongjing Hu, Shiling Wang, Jue Xue, Zhuoyin Wang, Cheng Wang, Nan |
author_sort | Zhang, Yongjing |
collection | PubMed |
description | The SARS-CoV-2 outbreak, began in late 2019, has caused a worldwide pandemic and shows no signs of slowing. Glucocorticoids (GCs), including dexamethasone (DEX), have been widely used as effective anti-inflammatory and immunosuppressant drugs. In this study, seven GCs had no obvious effect on cell viability of angiotensin converting enzyme 2 (ACE2) high expressed HEK293T cells when concentrations were under 10 μM. Molecular docking results revealed that DEX occupied with active binding site of ACE2 of SARS-CoV-2 spike protein. Surface plasmon resonance (SPR) results showed that K(D) value between DEX and ACE2 was (9.03 ± 0.78) e−6 M. Cell membrane chromatography (CMC) results uncovered that DEX had a chromatographic retention. DEX was found out to inhibiting the viropexis into ACE2(h) cells using SARS-CoV-2 spike pseudotyped virus. Therefore, DEX inhibits the entrance of SARS-CoV-2 spike pseudotyped virus into cell by binding to ACE2. |
format | Online Article Text |
id | pubmed-7744032 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77440322020-12-17 Dexamethasone inhibits SARS-CoV-2 spike pseudotyped virus viropexis by binding to ACE2 Zhang, Yongjing Hu, Shiling Wang, Jue Xue, Zhuoyin Wang, Cheng Wang, Nan Virology Article The SARS-CoV-2 outbreak, began in late 2019, has caused a worldwide pandemic and shows no signs of slowing. Glucocorticoids (GCs), including dexamethasone (DEX), have been widely used as effective anti-inflammatory and immunosuppressant drugs. In this study, seven GCs had no obvious effect on cell viability of angiotensin converting enzyme 2 (ACE2) high expressed HEK293T cells when concentrations were under 10 μM. Molecular docking results revealed that DEX occupied with active binding site of ACE2 of SARS-CoV-2 spike protein. Surface plasmon resonance (SPR) results showed that K(D) value between DEX and ACE2 was (9.03 ± 0.78) e−6 M. Cell membrane chromatography (CMC) results uncovered that DEX had a chromatographic retention. DEX was found out to inhibiting the viropexis into ACE2(h) cells using SARS-CoV-2 spike pseudotyped virus. Therefore, DEX inhibits the entrance of SARS-CoV-2 spike pseudotyped virus into cell by binding to ACE2. Elsevier Inc. 2021-02 2020-12-16 /pmc/articles/PMC7744032/ /pubmed/33387788 http://dx.doi.org/10.1016/j.virol.2020.12.001 Text en © 2020 Elsevier Inc. 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 Zhang, Yongjing Hu, Shiling Wang, Jue Xue, Zhuoyin Wang, Cheng Wang, Nan Dexamethasone inhibits SARS-CoV-2 spike pseudotyped virus viropexis by binding to ACE2 |
title | Dexamethasone inhibits SARS-CoV-2 spike pseudotyped virus viropexis by binding to ACE2 |
title_full | Dexamethasone inhibits SARS-CoV-2 spike pseudotyped virus viropexis by binding to ACE2 |
title_fullStr | Dexamethasone inhibits SARS-CoV-2 spike pseudotyped virus viropexis by binding to ACE2 |
title_full_unstemmed | Dexamethasone inhibits SARS-CoV-2 spike pseudotyped virus viropexis by binding to ACE2 |
title_short | Dexamethasone inhibits SARS-CoV-2 spike pseudotyped virus viropexis by binding to ACE2 |
title_sort | dexamethasone inhibits sars-cov-2 spike pseudotyped virus viropexis by binding to ace2 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7744032/ https://www.ncbi.nlm.nih.gov/pubmed/33387788 http://dx.doi.org/10.1016/j.virol.2020.12.001 |
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