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10.1002/pep2.24217

http://scihub22266oqcxt.onion/10.1002/pep2.24217
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33615115!7883042!33615115
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suck abstract from ncbi


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pmid33615115      Pept+Sci+(Hoboken) 2021 ; 113 (4): e24217
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  • Stapled ACE2 peptidomimetics designed to target the SARS-CoV-2 spike protein do not prevent virus internalization #MMPMID33615115
  • Morgan DC; Morris C; Mahindra A; Blair CM; Tejeda G; Herbert I; Turnbull ML; Lieber G; Willett BJ; Logan N; Smith B; Tobin AB; Bhella D; Baillie G; Jamieson AG
  • Pept Sci (Hoboken) 2021[Jul]; 113 (4): e24217 PMID33615115show ga
  • COVID-19 is caused by a novel coronavirus called severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2). Virus cell entry is mediated through a protein-protein interaction (PPI) between the SARS-CoV-2 spike protein and angiotensin-converting enzyme 2 (ACE2). A series of stapled peptide ACE2 peptidomimetics based on the ACE2 interaction motif were designed to bind the coronavirus S-protein RBD and inhibit binding to the human ACE2 receptor. The peptidomimetics were assessed for antiviral activity in an array of assays including a neutralization pseudovirus assay, immunofluorescence (IF) assay and in-vitro fluorescence polarization (FP) assay. However, none of the peptidomimetics showed activity in these assays, suggesting that an enhanced binding interface is required to outcompete ACE2 for S-protein RBD binding and prevent virus internalization.
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