Synthesis, insertion, and characterization of SARS-CoV-2 membrane protein within lipid bilayers
ORAL
Abstract
Throughout history, coronaviruses have posed challenges to both public health and the global economy; nevertheless, methods to combat them remain rudimentary, primarily due to the absence of experiments to understand the function of various viral components. Among these, membrane (M) proteins are one of the most elusive because of their small size and challenges with expression. In our work, we report the development of an expression system to produce tens to hundreds of milligrams of M protein per liter of Escherichia coli culture. These large yields render many previously inaccessible structural and biophysical experiments feasible. Using cryo–electron microscopy and atomic force microscopy, we image and characterize individual membrane-incorporated M protein dimers and discover membrane thinning in the vicinity, which we validated with molecular dynamics simulations. Our results suggest that the resulting line tension, along with predicted induction of local membrane curvature, could ultimately drive viral assembly and budding.
*This work was supported by University of California Office of the President UC Multicampus Research Programs and Initiatives, grant M21PR3267 (M.E.C., A.G., U.M., R.Z., and T.E.K.); National Science Foundation RAPID, grant 2034794 (U.M., R.Z., and T.E.K.); National Science Foundation, NSF DMR-2131963 (R.Z. and S.L.); National Science Foundation, NSF-CREST: Center for Cellular and Biomolecular Machines at UC Merced, NSF-HRD-1547848 and NSF-HRD-2112675 (A.G.); National Institutes of Health, NIH G-RISE, T32GM141862 (J.M. and A.G.); National Science Foundation, Center for Engineering Mechanobiology, grant CMMI-1548571 (A.G.); and National Science Foundation, Pinnacles Computing Cluster, NSF-ACI-2019144 (J.M.).
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Presenters
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sara anbir
- University of California, Riverside