bioRxiv · 10.1101/2020.07.22.215236
Virus-free and live-cell visualizing SARS-CoV-2 cell entry for studies of neutralizing antibodies and compound inhibitors
Abstract
The ongoing COVID-19 pandemic, caused by SARS-CoV-2 infection, has resulted in hundreds of thousands of deaths. Cellular entry of SARS-CoV-2, which is mediated by the viral spike protein and host ACE2 receptor, is an essential target for the development of vaccines, therapeutic antibodies, and drugs. Using a mammalian cell expression system, we generated a recombinant fluorescent protein (Gamillus)-fused SARS-CoV-2 spike trimer (STG) to probe the viral entry process. In ACE2-expressing cells, we found that the STG probe has excellent performance in the live-cell visualization of receptor binding, cellular uptake, and intracellular trafficking of SARS-CoV-2 under virus-free conditions. The new system allows quantitative analyses of the inhibition potentials and detailed influence of COVID-19-convalescent human plasmas, neutralizing antibodies and compounds, providing a versatile tool for high-throughput screening and phenotypic characterization of SARS-CoV-2 entry inhibitors. This approach may also be adapted to develop a viral entry visualization system for other viruses.
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Zhang, Y., Wang, S., Wu, Y., Hou, W., Yuan, L., Sheng, C., Wang, J., Ye, J., Zheng, Q., Ma, J., Xu, J., Wei, M., Li, Z., Nian, S., Xiong, H., Zhang, L., Shi, Y., Fu, B., Cao, J., Yang, C., Yang, T., Liu, L., Yu, H., Hu, J., Ge, S., Chen, Y., Zhang, T., Zhang, J., Cheng, T., Yuan, Q., Xia, N.. 2020-07-22. Virus-free and live-cell visualizing SARS-CoV-2 cell entry for studies of neutralizing antibodies and compound inhibitors. https://doi.org/10.1101/2020.07.22.215236
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