Crippling life support for SARS-CoV-2 and other viruses through synthetic lethality

Author:

Mast Fred D.1ORCID,Navare Arti T.1ORCID,van der Sloot Almer M.2ORCID,Coulombe-Huntington Jasmin2,Rout Michael P.3ORCID,Baliga Nitin S.4,Kaushansky Alexis15ORCID,Chait Brian T.6,Aderem Alan15,Rice Charles M.7ORCID,Sali Andrej8,Tyers Mike2ORCID,Aitchison John D.159ORCID

Affiliation:

1. Center for Global Infectious Disease Research, Seattle Children’s Research Institute, Seattle, WA

2. Institute for Research in Immunology and Cancer, Université de Montréal, Montreal, Canada

3. Laboratory of Cellular and Structural Biology, The Rockefeller University, New York, NY

4. Institute for Systems Biology, Seattle, WA

5. Department of Pediatrics, University of Washington, Seattle, WA

6. Laboratory of Mass Spectrometry and Gaseous Ion Chemistry, The Rockefeller University, New York, NY

7. Laboratory of Virology and Infectious Disease, The Rockefeller University, New York, NY

8. Department of Bioengineering and Therapeutic Sciences, Department of Pharmaceutical Chemistry, and California Institute for Quantitative Biosciences, University of California, San Francisco, San Francisco, CA

9. Department of Biochemistry, University of Washington, Seattle, WA

Abstract

With the rapid global spread of SARS-CoV-2, we have become acutely aware of the inadequacies of our ability to respond to viral epidemics. Although disrupting the viral life cycle is critical for limiting viral spread and disease, it has proven challenging to develop targeted and selective therapeutics. Synthetic lethality offers a promising but largely unexploited strategy against infectious viral disease; as viruses infect cells, they abnormally alter the cell state, unwittingly exposing new vulnerabilities in the infected cell. Therefore, we propose that effective therapies can be developed to selectively target the virally reconfigured host cell networks that accompany altered cellular states to cripple the host cell that has been converted into a virus factory, thus disrupting the viral life cycle.

Funder

National Institutes of Health

Canadian Institutes for Health Research

G. Harold and Leila Y. Mathers Charitable Foundation

George Mason University

Publisher

Rockefeller University Press

Subject

Cell Biology

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