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10.1002/smtd.202001031

http://scihub22266oqcxt.onion/10.1002/smtd.202001031
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33614907!7883248!33614907
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suck abstract from ncbi


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pmid33614907      Small+Methods 2021 ; 5 (2): 2001031
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  • Virus-Free and Live-Cell Visualizing SARS-CoV-2 Cell Entry for Studies of Neutralizing Antibodies and Compound Inhibitors #MMPMID33614907
  • Zhang Y; Wang S; Wu Y; Hou W; Yuan L; Shen 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; Li Z; Yang T; Liu L; Yu H; Hu J; Ge S; Chen Y; Zhang T; Zhang J; Cheng T; Yuan Q; Xia N
  • Small Methods 2021[Feb]; 5 (2): 2001031 PMID33614907show ga
  • The ongoing corona virus disease 2019 (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 ACE2 receptor, is an essential target for the development of vaccines, therapeutic antibodies, and drugs. Using a mammalian cell expression system, a genetically engineered sensor of fluorescent protein (Gamillus)-fused SARS-CoV-2 spike trimer (STG) to probe the viral entry process is developed. In ACE2-expressing cells, it is 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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