bioRxiv (Cold Spring Harbor Laboratory) · 2020 · 456 citations · 155 references
Life SciencesInfectious DiseasesMolecular BiologyMolecular VirologyProtein-protein InteractionsVirologyAntiviral PharmacologyAntiviral TherapyHost-virus InteractionsViral InfectionsAffinity PurificationAffinity Purification Mass SpectrometryHost Factor DependencyHost Factors In InfectionRepurposing Of Approved DrugsSars-cov-2 Antiviral TherapySars-cov-2 InfectionViral Therapeutic Targets
ABSTRACT An outbreak of the novel coronavirus SARS-CoV-2, the causative agent of COVID-19 respiratory disease, has infected over 290,000 people since the end of 2019, killed over 12,000, and caused worldwide social and economic disruption 1,2 . There are currently no antiviral drugs with proven efficacy nor are there vaccines for its prevention. Unfortunately, the scientific community has little knowledge of the molecular details of SARS-CoV-2 infection. To illuminate this, we cloned, tagged and expressed 26 of the 29 viral proteins in human cells and identified the human proteins physically associated with each using affinity-purification mass spectrometry (AP-MS), which identified 332 high confidence SARS-CoV-2-human protein-protein interactions (PPIs). Among these, we identify 67 druggable human proteins or host factors targeted by 69 existing FDA-approved drugs, drugs in clinical trials and/or preclinical compounds, that we are currently evaluating for efficacy in live SARS-CoV-2 infection assays. The identification of host dependency factors mediating virus infection may provide key insights into effective molecular targets for developing broadly acting antiviral therapeutics against SARS-CoV-2 and other deadly coronavirus strains.
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