Intrinsic furin-mediated cleavability of the spike S1/S2 site from SARS-CoV-2 variant B.1.1.529 (Omicron).


Journal

bioRxiv : the preprint server for biology
Titre abrégé: bioRxiv
Pays: United States
ID NLM: 101680187

Informations de publication

Date de publication:
26 Jul 2022
Historique:
pubmed: 5 8 2022
medline: 5 8 2022
entrez: 4 8 2022
Statut: epublish

Résumé

The ability of SARS-CoV-2 to be primed for viral entry by the host cell protease furin has become one of the most investigated of the numerous transmission and pathogenicity features of the virus. SARS-CoV-2 The variant B.1.1.529 (Omicron) emerged in late 2020 and has continued to evolve and is now present in several distinct sub-variants. Here, we analyzed the "furin cleavage site" of the spike protein of SARS-CoV-2 B.1.1.529 (Omicron variant)

Identifiants

pubmed: 35923311
doi: 10.1101/2022.04.20.488969
pmc: PMC9347273
pii:
doi:

Types de publication

Preprint

Langues

eng

Auteurs

Bailey Lubinski (B)

Graduate Field of Biological & Biomedical Sciences, Cornell University, Ithaca NY, 14853, USA.
Department of Microbiology & Immunology, College of Veterinary Medicine, Cornell University, Ithaca NY, 14853, USA.

Javier A Jaimes (JA)

Department of Microbiology & Immunology, College of Veterinary Medicine, Cornell University, Ithaca NY, 14853, USA.

Gary R Whittaker (GR)

Department of Microbiology & Immunology, College of Veterinary Medicine, Cornell University, Ithaca NY, 14853, USA.
Department of Public and Ecosystem Health, College of Veterinary Medicine, Cornell University, Ithaca NY, 14853, USA.

Classifications MeSH