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10.3390/ijms22126462

http://scihub22266oqcxt.onion/10.3390/ijms22126462
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34208755!8235207!34208755
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suck abstract from ncbi


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pmid34208755      Int+J+Mol+Sci 2021 ; 22 (12): ä
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  • More Is Always Better Than One: The N-Terminal Domain of the Spike Protein as Another Emerging Target for Hampering the SARS-CoV-2 Attachment to Host Cells #MMPMID34208755
  • Di Gaetano S; Capasso D; Delre P; Pirone L; Saviano M; Pedone E; Mangiatordi GF
  • Int J Mol Sci 2021[Jun]; 22 (12): ä PMID34208755show ga
  • Although the approved vaccines are proving to be of utmost importance in containing the Coronavirus disease 2019 (COVID-19) threat, they will hardly be resolutive as new severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2, a single-stranded RNA virus) variants might be insensitive to the immune response they induce. In this scenario, developing an effective therapy is still a dire need. Different targets for therapeutic antibodies and diagnostics have been identified, among which the SARS-CoV-2 spike (S) glycoprotein, particularly its receptor-binding domain, has been defined as crucial. In this context, we aim to focus attention also on the role played by the S N-terminal domain (S1-NTD) in the virus attachment, already recognized as a valuable target for neutralizing antibodies, in particular, building on a cavity mapping indicating the presence of two druggable pockets and on the recent literature hypothesizing the presence of a ganglioside-binding domain. In this perspective, we aim at proposing S1-NTD as a putative target for designing small molecules hopefully able to hamper the SARS-CoV-2 attachment to host cells.
  • |Binding Sites[MESH]
  • |COVID-19/pathology/therapy/virology[MESH]
  • |Drug Repositioning[MESH]
  • |Humans[MESH]
  • |Molecular Dynamics Simulation[MESH]
  • |N-Acetylneuraminic Acid/analogs & derivatives/metabolism/pharmacology/therapeutic use[MESH]
  • |Protein Binding[MESH]
  • |Protein Domains[MESH]
  • |SARS-CoV-2/isolation & purification/*metabolism[MESH]
  • |Small Molecule Libraries/chemistry/metabolism/pharmacology/therapeutic use[MESH]
  • |Spike Glycoprotein, Coronavirus/chemistry/*metabolism[MESH]


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