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10.1016/j.scib.2021.01.010

http://scihub22266oqcxt.onion/10.1016/j.scib.2021.01.010
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33495714!7816574!33495714
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suck abstract from ncbi

pmid33495714      Sci+Bull+(Beijing) 2021 ; 66 (12): 1205-1214
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  • Binding of the SARS-CoV-2 spike protein to glycans #MMPMID33495714
  • Hao W; Ma B; Li Z; Wang X; Gao X; Li Y; Qin B; Shang S; Cui S; Tan Z
  • Sci Bull (Beijing) 2021[Jun]; 66 (12): 1205-1214 PMID33495714show ga
  • The pandemic of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has caused a high number of deaths in the world. To combat it, it is necessary to develop a better understanding of how the virus infects host cells. Infection normally starts with the attachment of the virus to cell-surface glycans like heparan sulfate (HS) and sialic acid-containing glycolipids/glycoproteins. In this study, we examined and compared the binding of the subunits and spike (S) proteins of SARS-CoV-2, SARS-CoV, and Middle East respiratory disease (MERS)-CoV to these glycans. Our results revealed that the S proteins and subunits can bind to HS in a sulfation-dependent manner and no binding with sialic acid residues was detected. Overall, this work suggests that HS binding may be a general mechanism for the attachment of these coronaviruses to host cells, and supports the potential importance of HS in infection and in the development of antiviral agents against these viruses.
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