Leibniz Institute - Isopeptide analysis

Comprehensive Detection of Isopeptides between Human Tissue Transglutaminase and Gluten Peptides
Data License: CC BY 4.0
  • Organism: Triticum, human
  • Instrument: Q Exactive HF
  • SpikeIn: No
  • Keywords: celiac disease; crosslink; deamidation; gliadin; gluten; isopeptides; LC-MS/MS; tissue transglutaminase; transamidation
  • Lab head: Katharina Scherf Submitter: Barbara Lexhaller
Celiac disease (CD) is a chronic inflammation of the small intestine triggered by the ingestion of gluten in genetically predisposed individuals. Tissue transglutaminase (TG2) is a key factor in CD pathogenesis, because it catalyzes both the deamidation of specific glutamine residues and the formation of covalent Nε-(γ-glutamyl)-lysine isopeptide crosslinks resulting in TG2–gluten peptide complexes. These complexes are thought to activate B cells causing the secretion of anti-TG2 autoantibodies that serve as diagnostic markers for CD, although their pathogenic role remains unclear. To gain more insight into the molecular structures of TG2-gluten peptide complexes, we used different proteomics software tools that enable the comprehensive identification of isopeptides. Thus, 34 different isopeptides involving 20 TG2 lysine residues were identified in a model system, only six of which were previously known. Additionally, 36 isopeptides of TG2-TG2 multimers were detected. Experiments with different TG2-gluten peptide molar ratios revealed the most preferred lysine residues involved in isopeptide crosslinking. Expanding the model system to three gluten peptides with more glutamine residues allowed the localization of the preferred glutamine crosslinking sites. These new insights into the structure of TG2-gluten peptide complexes may help clarify the role of extracellular TG2 in CD autoimmunity and in other inflammatory diseases.
Created on 9/28/19, 12:44 PM

Raw data files for this work are available in PRIDE under the ProteomeXchange ID PXD014067

This data is available under the CC BY 4.0 license.