Abstract
Major histocompatibility complex (MHC, or human leukocyte antigen, HLA) peptide ligands can be exploited to develop immunotherapies targeting immunogenic disease-specific immunopeptides, such as virus- or cancer mutation-derived peptides. Liquid chromatography coupled with mass spectrometry (LC-MS)-based immunopeptidomics is the gold standard for identifying MHC ligands. We previously optimized a workflow enabling the identification of more than 10,000 MHC class I ligands per cell line. This process comprises three major steps: (I) a high-recovery immunopeptidome enrichment, (II) an optimized MS acquisition in the timsTOF Pro called Thunder-Data-Dependent Acquisition with Parallel Accumulation-SErial Fragmentation (Thunder-DDA-PASEF), and (III) peptide identification using PEAKS XPro boosted by MS2Rescore data-driven rescoring. Here, we describe our workflow for deep-coverage immunopeptidomics step-by-step, from sample preparation to data analysis and validation.
Author supplied keywords
Cite
CITATION STYLE
Gomez-Zepeda, D., Beyrle, J., Preikschat, A., Declercq, A., Chen, Y., Gabriels, R., … Tenzer, S. (2026). High-Coverage Immunopeptidomics Using timsTOF Mass Spectrometers with Thunder-DDA-PASEF Boosted by MS2Rescore. In Methods in Molecular Biology (Vol. 2980, pp. 115–155). Humana Press Inc. https://doi.org/10.1007/978-1-0716-4832-2_5
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.