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Targeting ACE2-RBD interaction as a platform for COVID19 therapeutics: Development and drug repurposing screen of an AlphaLISA proximity assay
The COVID-19 pandemic, caused by SARS-CoV-2, is a pressing public health emergency garnering rapid response from scientists across the globe. Host cell invasion is initiated through direct binding of the viral spike protein to the host receptor angiotensin-converting enzyme 2 (ACE2). Disrupting the...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7301901/ https://www.ncbi.nlm.nih.gov/pubmed/32577632 http://dx.doi.org/10.1101/2020.06.16.154708 |
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author | Hanson, Quinlin M. Wilson, Kelli M. Shen, Min Itkin, Zina Eastman, Richard T. Shinn, Paul Hall, Matthew D. |
author_facet | Hanson, Quinlin M. Wilson, Kelli M. Shen, Min Itkin, Zina Eastman, Richard T. Shinn, Paul Hall, Matthew D. |
author_sort | Hanson, Quinlin M. |
collection | PubMed |
description | The COVID-19 pandemic, caused by SARS-CoV-2, is a pressing public health emergency garnering rapid response from scientists across the globe. Host cell invasion is initiated through direct binding of the viral spike protein to the host receptor angiotensin-converting enzyme 2 (ACE2). Disrupting the spike-ACE2 interaction is a potential therapeutic target for treating COVID-19. We have developed a proximity-based AlphaLISA assay to measure binding of SARS-CoV-2 spike protein Receptor Binding Domain (RBD) to ACE2. Utilizing this assay platform, a drug-repurposing screen against 3,384 small molecule drugs and pre-clinical compounds was performed, yielding 25 high-quality, small-molecule hits that can be evaluated in cell-based models. This established AlphaLISA RBD-ACE2 platform can facilitate evaluation of biologics or small molecules that can perturb this essential viral-host interaction to further the development of interventions to address the global health pandemic. |
format | Online Article Text |
id | pubmed-7301901 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-73019012020-06-23 Targeting ACE2-RBD interaction as a platform for COVID19 therapeutics: Development and drug repurposing screen of an AlphaLISA proximity assay Hanson, Quinlin M. Wilson, Kelli M. Shen, Min Itkin, Zina Eastman, Richard T. Shinn, Paul Hall, Matthew D. bioRxiv Article The COVID-19 pandemic, caused by SARS-CoV-2, is a pressing public health emergency garnering rapid response from scientists across the globe. Host cell invasion is initiated through direct binding of the viral spike protein to the host receptor angiotensin-converting enzyme 2 (ACE2). Disrupting the spike-ACE2 interaction is a potential therapeutic target for treating COVID-19. We have developed a proximity-based AlphaLISA assay to measure binding of SARS-CoV-2 spike protein Receptor Binding Domain (RBD) to ACE2. Utilizing this assay platform, a drug-repurposing screen against 3,384 small molecule drugs and pre-clinical compounds was performed, yielding 25 high-quality, small-molecule hits that can be evaluated in cell-based models. This established AlphaLISA RBD-ACE2 platform can facilitate evaluation of biologics or small molecules that can perturb this essential viral-host interaction to further the development of interventions to address the global health pandemic. Cold Spring Harbor Laboratory 2020-06-16 /pmc/articles/PMC7301901/ /pubmed/32577632 http://dx.doi.org/10.1101/2020.06.16.154708 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/It is made available under a CC-BY 4.0 International license (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Article Hanson, Quinlin M. Wilson, Kelli M. Shen, Min Itkin, Zina Eastman, Richard T. Shinn, Paul Hall, Matthew D. Targeting ACE2-RBD interaction as a platform for COVID19 therapeutics: Development and drug repurposing screen of an AlphaLISA proximity assay |
title | Targeting ACE2-RBD interaction as a platform for COVID19 therapeutics: Development and drug repurposing screen of an AlphaLISA proximity assay |
title_full | Targeting ACE2-RBD interaction as a platform for COVID19 therapeutics: Development and drug repurposing screen of an AlphaLISA proximity assay |
title_fullStr | Targeting ACE2-RBD interaction as a platform for COVID19 therapeutics: Development and drug repurposing screen of an AlphaLISA proximity assay |
title_full_unstemmed | Targeting ACE2-RBD interaction as a platform for COVID19 therapeutics: Development and drug repurposing screen of an AlphaLISA proximity assay |
title_short | Targeting ACE2-RBD interaction as a platform for COVID19 therapeutics: Development and drug repurposing screen of an AlphaLISA proximity assay |
title_sort | targeting ace2-rbd interaction as a platform for covid19 therapeutics: development and drug repurposing screen of an alphalisa proximity assay |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7301901/ https://www.ncbi.nlm.nih.gov/pubmed/32577632 http://dx.doi.org/10.1101/2020.06.16.154708 |
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