Mapping the SARS-CoV-2 spike glycoprotein-derived peptidome presented by HLA class II on dendritic cells
Author(s) -
Robert Parker,
Thomas Partridge,
Catherine Wormald,
Rebeca Kawahara,
Victoria Stalls,
Maria Aggelakopoulou,
Jimmy Parker,
Rebecca Powell Doherty,
Yoanna Ariosa Morejon,
Esther Lee,
Kevin O. Saunders,
Barton F. Haynes,
Priyamvada Acharya,
Morten ThaysenAndersen,
Persephone Borrow,
Nicola Ternette
Publication year - 2021
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2021.109179
Subject(s) - human leukocyte antigen , glycoprotein , glycan , biology , immunology , glycosylation , immune system , hla dr , peptide vaccine , peptide , virology , antigen , computational biology , epitope , genetics , biochemistry
Summary Understanding and eliciting protective immune responses to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is an urgent priority. To facilitate these objectives, we profile the repertoire of human leukocyte antigen class II (HLA-II)-bound peptides presented by HLA-DR diverse monocyte-derived dendritic cells pulsed with SARS-CoV-2 spike (S) protein. We identify 209 unique HLA-II-bound peptide sequences, many forming nested sets, which map to sites throughout S including glycosylated regions. Comparison of the glycosylation profile of the S protein to that of the HLA-II-bound S peptides reveals substantial trimming of glycan residues on the latter, likely induced during antigen processing. Our data also highlight the receptor-binding motif in S1 as a HLA-DR-binding peptide-rich region and identify S2-derived peptides with potential for targeting by cross-protective vaccine-elicited responses. Results from this study will aid analysis of CD4 + T cell responses in infected individuals and vaccine recipients and have application in next-generation vaccine design.
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