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10.1016/j.celrep.2021.109433

http://scihub22266oqcxt.onion/10.1016/j.celrep.2021.109433
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suck abstract from ncbi


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pmid34273271      Cell+Rep 2021 ; 36 (4): 109433
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  • A SARS-CoV-2 neutralizing antibody selected from COVID-19 patients binds to the ACE2-RBD interface and is tolerant to most known RBD mutations #MMPMID34273271
  • Bertoglio F; Fuhner V; Ruschig M; Heine PA; Abassi L; Klunemann T; Rand U; Meier D; Langreder N; Steinke S; Ballmann R; Schneider KT; Roth KDR; Kuhn P; Riese P; Schackermann D; Korn J; Koch A; Chaudhry MZ; Eschke K; Kim Y; Zock-Emmenthal S; Becker M; Scholz M; Moreira GMSG; Wenzel EV; Russo G; Garritsen HSP; Casu S; Gerstner A; Roth G; Adler J; Trimpert J; Hermann A; Schirrmann T; Dubel S; Frenzel A; Van den Heuvel J; Cicin-Sain L; Schubert M; Hust M
  • Cell Rep 2021[Jul]; 36 (4): 109433 PMID34273271show ga
  • The novel betacoronavirus severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) causes a form of severe pneumonia disease called coronavirus disease 2019 (COVID-19). To develop human neutralizing anti-SARS-CoV-2 antibodies, antibody gene libraries from convalescent COVID-19 patients were constructed and recombinant antibody fragments (scFv) against the receptor-binding domain (RBD) of the spike protein were selected by phage display. The antibody STE90-C11 shows a subnanometer IC(50) in a plaque-based live SARS-CoV-2 neutralization assay. The in vivo efficacy of the antibody is demonstrated in the Syrian hamster and in the human angiotensin-converting enzyme 2 (hACE2) mice model. The crystal structure of STE90-C11 Fab in complex with SARS-CoV-2-RBD is solved at 2.0 A resolution showing that the antibody binds at the same region as ACE2 to RBD. The binding and inhibition of STE90-C11 is not blocked by many known emerging RBD mutations. STE90-C11-derived human IgG1 with FcgammaR-silenced Fc (COR-101) is undergoing Phase Ib/II clinical trials for the treatment of moderate to severe COVID-19.
  • |Antibodies, Neutralizing/*immunology[MESH]
  • |Antibodies, Viral/*immunology[MESH]
  • |COVID-19/virology[MESH]
  • |Humans[MESH]
  • |Mutation/genetics[MESH]
  • |Peptidyl-Dipeptidase A/metabolism[MESH]
  • |Protein Binding[MESH]
  • |Protein Domains/genetics[MESH]
  • |SARS-CoV-2/*pathogenicity[MESH]


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