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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.
Afiliación
  • Hanson QM; National Center for Advancing Translational Sciences, National Institutes of Health.
  • Wilson KM; National Center for Advancing Translational Sciences, National Institutes of Health.
  • Shen M; National Center for Advancing Translational Sciences, National Institutes of Health.
  • Itkin Z; National Center for Advancing Translational Sciences, National Institutes of Health.
  • Eastman RT; National Center for Advancing Translational Sciences, National Institutes of Health.
  • Shinn P; National Center for Advancing Translational Sciences, National Institutes of Health.
  • Hall MD; National Center for Advancing Translational Sciences, National Institutes of Health.
bioRxiv ; 2020 Jun 16.
Article en En | MEDLINE | ID: mdl-32577632
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.