<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Leddy O</submitter><funding>U.S. Department of Health &amp;amp; Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID)</funding><funding>NIAID NIH HHS</funding><funding>NIEHS NIH HHS</funding><funding>NCI NIH HHS</funding><funding>NIGMS NIH HHS</funding><funding>U.S. Department of Health &amp;amp; Human Services | NIH | National Institute of General Medical Sciences (NIGMS)</funding><pagination>1196-1222</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12012165</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(5)</volume><pubmed_abstract>Vaccines and immunotherapies that target peptide-major histocompatibility complexes (peptide-MHCs) have the potential to address multiple unmet medical needs in cancer and infectious disease. Designing vaccines and immunotherapies to target peptide-MHCs requires accurate identification of target peptides in infected or cancerous cells or tissue, and may require absolute or relative quantification to identify abundant targets and measure changes in presentation under different treatment conditions. Internal standard parallel reaction monitoring (also known as 'SureQuant') can be used to validate and/or quantify MHC peptides previously identified by using untargeted methods such as data-dependent acquisition. SureQuant MHC has three main use cases: (i) conclusive confirmation of the identiti</pubmed_abstract><journal>Nature protocols</journal><pubmed_title>Validation and quantification of peptide antigens presented on MHCs using SureQuant.</pubmed_title><pmcid>PMC12012165</pmcid><funding_grant_id>1R35GM142900</funding_grant_id><funding_grant_id>R35 GM142900</funding_grant_id><funding_grant_id>U54 CA283114</funding_grant_id><funding_grant_id>R01 AI022553</funding_grant_id><funding_grant_id>P30 AI060354</funding_grant_id><funding_grant_id>R01AI022553</funding_grant_id><funding_grant_id>P42 ES027707</funding_grant_id><funding_grant_id>U01 CA238720</funding_grant_id><pubmed_authors>Kim DH</pubmed_authors><pubmed_authors>Bryson BD</pubmed_authors><pubmed_authors>Choe E</pubmed_authors><pubmed_authors>White FM</pubmed_authors><pubmed_authors>Cui Y</pubmed_authors><pubmed_authors>Spranger S</pubmed_authors><pubmed_authors>Stopfer L</pubmed_authors><pubmed_authors>Leddy O</pubmed_authors><pubmed_authors>Roerden M</pubmed_authors><pubmed_authors>Ahn R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Validation and quantification of peptide antigens presented on MHCs using SureQuant.</name><description>Vaccines and immunotherapies that target peptide-major histocompatibility complexes (peptide-MHCs) have the potential to address multiple unmet medical needs in cancer and infectious disease. Designing vaccines and immunotherapies to target peptide-MHCs requires accurate identification of target peptides in infected or cancerous cells or tissue, and may require absolute or relative quantification to identify abundant targets and measure changes in presentation under different treatment conditions. Internal standard parallel reaction monitoring (also known as 'SureQuant') can be used to validate and/or quantify MHC peptides previously identified by using untargeted methods such as data-dependent acquisition. SureQuant MHC has three main use cases: (i) conclusive confirmation of the identiti</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 May</publication><modification>2026-06-05T07:37:54.948Z</modification><creation>2026-05-14T03:12:47.156Z</creation></dates><accession>S-EPMC12012165</accession><cross_references><pubmed>39438697</pubmed><doi>10.1038/s41596-024-01076-x</doi></cross_references></HashMap>