<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Braun A</submitter><funding>National Psoriasis Foundation (NPF)</funding><funding>Rebecca L. Cooper Medical Research Foundation</funding><funding>Department of Health | National Health and Medical Research Council (NHMRC)</funding><pagination>7547</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11364864</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(1)</volume><pubmed_abstract>Most COVID-19 vaccines elicit immunity against the SARS-CoV-2 Spike protein. However, Spike protein mutations in emerging strains and immune evasion by the SARS-CoV-2 virus demonstrates the need to develop more broadly targeting vaccines. To facilitate this, we use mass spectrometry to identify immunopeptides derived from seven relatively conserved structural and non-structural SARS-CoV-2 proteins (N, E, Nsp1/4/5/8/9). We use two different B-lymphoblastoid cell lines to map Human Leukocyte Antigen (HLA) class I and class II immunopeptidomes covering some of the prevalent HLA types across the global human population. We employ DNA plasmid transfection and direct antigen delivery approaches to sample different antigens and find 248 unique HLA class I and HLA class II bound peptides with 71 d</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Mapping the immunopeptidome of seven SARS-CoV-2 antigens across common HLA haplotypes.</pubmed_title><pmcid>PMC11364864</pmcid><funding_grant_id>1194036</funding_grant_id><funding_grant_id>2016596</funding_grant_id><funding_grant_id>1143366</funding_grant_id><funding_grant_id>817907</funding_grant_id><funding_grant_id>2026357</funding_grant_id><funding_grant_id>1173871</funding_grant_id><funding_grant_id>PG2020775</funding_grant_id><pubmed_authors>Scull KE</pubmed_authors><pubmed_authors>Rowntree LC</pubmed_authors><pubmed_authors>Rossjohn J</pubmed_authors><pubmed_authors>Illing PT</pubmed_authors><pubmed_authors>Petersen J</pubmed_authors><pubmed_authors>Ayala R</pubmed_authors><pubmed_authors>Faridi P</pubmed_authors><pubmed_authors>Kringelum J</pubmed_authors><pubmed_authors>Braun A</pubmed_authors><pubmed_authors>Littler DR</pubmed_authors><pubmed_authors>Ramarathinam S</pubmed_authors><pubmed_authors>Chung S</pubmed_authors><pubmed_authors>Purcell AW</pubmed_authors><pubmed_authors>Thuesen N</pubmed_authors><pubmed_authors>Li C</pubmed_authors><pubmed_authors>Croft NP</pubmed_authors><pubmed_authors>Pandey K</pubmed_authors><pubmed_authors>Persson G</pubmed_authors><pubmed_authors>Jappe Lange E</pubmed_authors><pubmed_authors>Schantz Klausen M</pubmed_authors><pubmed_authors>Mifsud NA</pubmed_authors><pubmed_authors>Huang Z</pubmed_authors><pubmed_authors>Raji S</pubmed_authors><pubmed_authors>Kedzierska K</pubmed_authors><pubmed_authors>Nguyen THO</pubmed_authors><pubmed_authors>Sorensen AB</pubmed_authors></additional><is_claimable>false</is_claimable><name>Mapping the immunopeptidome of seven SARS-CoV-2 antigens across common HLA haplotypes.</name><description>Most COVID-19 vaccines elicit immunity against the SARS-CoV-2 Spike protein. However, Spike protein mutations in emerging strains and immune evasion by the SARS-CoV-2 virus demonstrates the need to develop more broadly targeting vaccines. To facilitate this, we use mass spectrometry to identify immunopeptides derived from seven relatively conserved structural and non-structural SARS-CoV-2 proteins (N, E, Nsp1/4/5/8/9). We use two different B-lymphoblastoid cell lines to map Human Leukocyte Antigen (HLA) class I and class II immunopeptidomes covering some of the prevalent HLA types across the global human population. We employ DNA plasmid transfection and direct antigen delivery approaches to sample different antigens and find 248 unique HLA class I and HLA class II bound peptides with 71 d</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Aug</publication><modification>2026-07-16T07:21:36.464Z</modification><creation>2025-04-06T13:45:25.132Z</creation></dates><accession>S-EPMC11364864</accession><cross_references><pubmed>39214998</pubmed><doi>10.1038/s41467-024-51959-6</doi></cross_references></HashMap>