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Mapping the SARS-CoV-2 spike glycoprotein-derived peptidome presented by HLA class II on dendritic cells
Robert Parker; Thomas Partridge; Catherine Wormald; Rebeca Kawahara; Victoria Stalls; Maria Aggelakopoulou; Jimmy Parker; Rebecca Powell Doherty; Yoanna Ariosa-Morejon; Esther Lee; Kevin Saunders; Barton F. Haynes; Priyamvada Acharya; Morten Thaysen-Andersen; Persephone Borrow; Nicola Ternette.
Affiliation
  • Robert Parker; University of Oxford, Oxford, OX3 7BN, United Kingdom
  • Thomas Partridge; University of Oxford, Oxford, OX3 7FZ, United Kingdom
  • Catherine Wormald; University of Oxford, Oxford, OX3 7FZ, United Kingdom
  • Rebeca Kawahara; Macquarie University, Sydney, New South Wales 2109, Australia
  • Victoria Stalls; Duke University, , Durham, NC 27710, USA
  • Maria Aggelakopoulou; University of Oxford, Oxford, OX3 7FZ, United Kingdom
  • Jimmy Parker; Wellbeing Software, Mansfield, NG18 5FB, United Kingdom
  • Rebecca Powell Doherty; University of Oxford, Oxford, OX3 7BN, United Kingdom
  • Yoanna Ariosa-Morejon; University of Oxford, Oxford, OX37FZ, United Kingdom
  • Esther Lee; Duke University School of Medicine, Durham, NC 27710, USA
  • Kevin Saunders; Duke University, Durham, NC 27710, USA
  • Barton F. Haynes; Duke University, Durham, NC 27710, USA
  • Priyamvada Acharya; Duke University, Durham, NC 27710, USA
  • Morten Thaysen-Andersen; Macquarie University, Sydney, New South Wales 2109, Australia
  • Persephone Borrow; University of Oxford, Oxford, OX37FZ, United Kingdom
  • Nicola Ternette; Universtiy of Oxford, Oxford, OX3 7BN, United Kingdom
Preprint in En | PREPRINT-BIORXIV | ID: ppbiorxiv-255901
Journal article
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ABSTRACT
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 have profiled 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 revealed substantial trimming of glycan residues on the latter, likely introduced during antigen processing. Our data also highlight the receptor-binding motif in S1 as a HLA-DR-binding peptide-rich region. Results from this study have application in vaccine design, and will aid analysis of CD4+ T cell responses in infected individuals and vaccine recipients.
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Full text: 1 Collection: 09-preprints Database: PREPRINT-BIORXIV Language: En Year: 2020 Type: Preprint
Full text: 1 Collection: 09-preprints Database: PREPRINT-BIORXIV Language: En Year: 2020 Type: Preprint