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10.1002/biot.202000566

http://scihub22266oqcxt.onion/10.1002/biot.202000566
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33481336!7995010!33481336
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suck abstract from ncbi


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pmid33481336      Biotechnol+J 2021 ; 16 (6): e2000566
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  • Generation of enzymatically competent SARS-CoV-2 decoy receptor ACE2-Fc in glycoengineered Nicotiana benthamiana #MMPMID33481336
  • Castilho A; Schwestka J; Kienzl NF; Vavra U; Grunwald-Gruber C; Izadi S; Hiremath C; Niederhofer J; Laurent E; Monteil V; Mirazimi A; Wirnsberger G; Stadlmann J; Stoger E; Mach L; Strasser R
  • Biotechnol J 2021[Jun]; 16 (6): e2000566 PMID33481336show ga
  • Human angiotensin-converting enzyme 2 (ACE2) is the primary host cell receptor for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) binding and cell entry. Administration of high concentrations of soluble ACE2 can be utilized as a decoy to block the interaction of the virus with cellular ACE2 receptors and potentially be used as a strategy for treatment or prevention of coronavirus disease 2019. Human ACE2 is heavily glycosylated and its glycans impact on binding to the SARS-CoV-2 spike protein and virus infectivity. Here, we describe the production of a recombinant soluble ACE2-fragment crystallizable (Fc) variant in glycoengineered Nicotiana benthamiana. Our data reveal that the produced dimeric ACE2-Fc variant is glycosylated with mainly complex human-type N-glycans and functional with regard to enzyme activity, affinity to the SARS-CoV-2 receptor-binding domain, and wild-type virus neutralization.
  • |*COVID-19[MESH]
  • |*SARS-CoV-2[MESH]
  • |Angiotensin-Converting Enzyme 2[MESH]
  • |Humans[MESH]
  • |Nicotiana/genetics/metabolism[MESH]
  • |Peptidyl-Dipeptidase A/genetics/metabolism[MESH]
  • |Protein Binding[MESH]


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