The E484K mutation in the SARS-CoV-2 spike protein reduces but does not abolish neutralizing activity of human convalescent and post-vaccination sera.


Journal

medRxiv : the preprint server for health sciences
Titre abrégé: medRxiv
Pays: United States
ID NLM: 101767986

Informations de publication

Date de publication:
29 Jan 2021
Historique:
pubmed: 4 2 2021
medline: 4 2 2021
entrez: 3 2 2021
Statut: epublish

Résumé

One year in the coronavirus disease 2019 (COVID-19) pandemic, the first vaccines are being rolled out under emergency use authorizations. It is of great concern that newly emerging variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) can escape antibody-mediated protection induced by previous infection or vaccination through mutations in the spike protein. The glutamate (E) to Lysine (K) substitution at position 484 (E484K) in the receptor binding domain (RBD) of the spike protein is present in the rapidly spreading variants of concern belonging to the B.1.351 and P.1 lineages. We performed

Identifiants

pubmed: 33532796
doi: 10.1101/2021.01.26.21250543
pmc: PMC7852247
pii:
doi:

Types de publication

Preprint

Langues

eng

Subventions

Organisme : NIAID NIH HHS
ID : 75N93019C00051
Pays : United States
Organisme : NIAID NIH HHS
ID : HHSN272201400005C
Pays : United States
Organisme : NIAID NIH HHS
ID : HHSN272201400008C
Pays : United States
Organisme : NCI NIH HHS
ID : U54 CA260560
Pays : United States

Auteurs

Sonia Jangra (S)

Department of Microbiology, Icahn School of Medicine at Mount Sinai New York, NY, USA.
Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai New York, NY, USA.

Chengjin Ye (C)

Texas Biomedical Research Institute, San Antonio, TX, USA.

Raveen Rathnasinghe (R)

Department of Microbiology, Icahn School of Medicine at Mount Sinai New York, NY, USA.
Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai New York, NY, USA.
Graduate School of Biomedical Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Daniel Stadlbauer (D)

Department of Microbiology, Icahn School of Medicine at Mount Sinai New York, NY, USA.

Florian Krammer (F)

Department of Microbiology, Icahn School of Medicine at Mount Sinai New York, NY, USA.

Viviana Simon (V)

Department of Microbiology, Icahn School of Medicine at Mount Sinai New York, NY, USA.
Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai New York, NY, USA.
Department of Medicine, Division of Infectious Diseases, Icahn School of Medicine at Mount Sinai New York, NY, USA.

Luis Martinez-Sobrido (L)

Texas Biomedical Research Institute, San Antonio, TX, USA.

Adolfo García-Sastre (A)

Department of Microbiology, Icahn School of Medicine at Mount Sinai New York, NY, USA.
Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai New York, NY, USA.
Department of Medicine, Division of Infectious Diseases, Icahn School of Medicine at Mount Sinai New York, NY, USA.
The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai New York, NY, USA.

Michael Schotsaert (M)

Department of Microbiology, Icahn School of Medicine at Mount Sinai New York, NY, USA.
Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai New York, NY, USA.

Classifications MeSH