High-coverage immunopeptidomics using timsTOF mass spectrometers with Thunder-DDA-PASEF boosted by MS2Rescore

Author:

Gomez-Zepeda David1ORCID,Beyrle Julian1ORCID,Preikschat Annica2,Declercq Arthur3ORCID,Chen Yannic1,Gabriels Ralf3ORCID,Martens Lennart3ORCID,Distler Ute2ORCID,Tenzer Stefan4ORCID

Affiliation:

1. Helmholtz Institute for Translational Oncology Mainz (HI-TRON Mainz) – A Helmholtz Institute of the DKFZ, Mainz, Germany; DKFZ German Cancer Research Center, Heidelberg, Germany

2. Institute of Immunology, University Medical Center Mainz, Mainz, Germany

3. Gent University, Gent, Belgium

4. Helmholtz Institute for Translational Oncology Mainz (HI-TRON Mainz) – A Helmholtz Institute of the DKFZ, Mainz, Germany; DKFZ German Cancer Research Center, Heidelberg, Germany; Institute of Immunology, University Medical Center Mainz, Mainz, Germany

Abstract

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), (III) and 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.

Publisher

Springer Science and Business Media LLC

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