<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>26(10)</volume><submitter>Kormann K</submitter><pubmed_abstract>Immunoassays for cardiac troponin, such as the Elecsys&lt;sup>®&lt;/sup> hs-TnT, have become the gold standard for myocardial infarction diagnostics. While various protein/chemical factors affecting the troponin complex and thus its diagnostic accuracy have been investigated, the role of coding single-nucleotide polymorphisms remains underexplored. To evaluate potential cSNP-induced interference with antibody binding in the Elecsys&lt;sup>®&lt;/sup> hs-TnT immunoassay, we applied ITEM-FOUR, a mass spectrometry-based method that quantifies changes in antibody binding upon amino acid substitutions in epitope peptides. Candidate cSNPs were selected from the dbSNP database and were mapped to human cardiac troponin T by molecular modeling. Consuming micromolar antibody concentrations and microliter sample </pubmed_abstract><journal>International journal of molecular sciences</journal><pagination>4892</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12112476</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Mass Spectrometric ITEM-FOUR Analysis Reveals Coding Single-Nucleotide Polymorphisms in Human Cardiac Troponin T That Evade Detection by Sandwich ELISAs Which Use Monoclonal Antibodies M7 and M11.7 from the Elecsys Troponin T&amp;lt;sup&amp;gt;®&amp;lt;/sup&amp;gt; Assay.</pubmed_title><pmcid>PMC12112476</pmcid><pubmed_authors>Glocker MO</pubmed_authors><pubmed_authors>Ruß M</pubmed_authors><pubmed_authors>Kormann K</pubmed_authors><pubmed_authors>Koy C</pubmed_authors><pubmed_authors>Rower C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Mass Spectrometric ITEM-FOUR Analysis Reveals Coding Single-Nucleotide Polymorphisms in Human Cardiac Troponin T That Evade Detection by Sandwich ELISAs Which Use Monoclonal Antibodies M7 and M11.7 from the Elecsys Troponin T&amp;lt;sup&amp;gt;®&amp;lt;/sup&amp;gt; Assay.</name><description>Immunoassays for cardiac troponin, such as the Elecsys&lt;sup>®&lt;/sup> hs-TnT, have become the gold standard for myocardial infarction diagnostics. While various protein/chemical factors affecting the troponin complex and thus its diagnostic accuracy have been investigated, the role of coding single-nucleotide polymorphisms remains underexplored. To evaluate potential cSNP-induced interference with antibody binding in the Elecsys&lt;sup>®&lt;/sup> hs-TnT immunoassay, we applied ITEM-FOUR, a mass spectrometry-based method that quantifies changes in antibody binding upon amino acid substitutions in epitope peptides. Candidate cSNPs were selected from the dbSNP database and were mapped to human cardiac troponin T by molecular modeling. Consuming micromolar antibody concentrations and microliter sample </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 May</publication><modification>2026-05-23T03:12:46.913Z</modification><creation>2026-05-23T03:08:16.556Z</creation></dates><accession>S-EPMC12112476</accession><cross_references><pubmed>40430031</pubmed><doi>10.3390/ijms26104892</doi></cross_references></HashMap>