Synthesis, insertion, and characterization of SARS-CoV-2 membrane protein within lipid bilayers

Author:

Zhang Yuanzhong1ORCID,Anbir Sara2ORCID,McTiernan Joseph3ORCID,Li Siyu1,Worcester Michael1,Mishra Pratyasha4ORCID,Colvin Michael E.5ORCID,Gopinathan Ajay3ORCID,Mohideen Umar12,Zandi Roya12,Kuhlman Thomas E.126ORCID

Affiliation:

1. Department of Physics and Astronomy, University of California, Riverside, Riverside, CA 92521, USA.

2. Biophysics Program, University of California, Riverside, Riverside, CA 92521, USA.

3. Department of Physics, University of California, Merced, Merced, CA 95340, USA.

4. Department of Biochemistry, University of California, Riverside, Riverside, CA 92521, USA.

5. Department of Chemistry and Biochemistry, University of California, Merced, Merced, CA 95340, USA.

6. Microbiology Program, University of California, Riverside, Riverside, CA 92521, USA.

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. Here, 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.

Publisher

American Association for the Advancement of Science (AAAS)

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