Crucial Parameters for Immunopeptidome Characterization: A Systematic Evaluation

Author:

Juanes-Velasco Pablo123ORCID,Arias-Hidalgo Carlota123ORCID,García-Vaquero Marina L.123,Sotolongo-Ravelo Janet4ORCID,Paíno Teresa45ORCID,Lécrevisse Quentin123ORCID,Landeira-Viñuela Alicia123,Góngora Rafael123ORCID,Hernández Ángela-Patricia1236ORCID,Fuentes Manuel1237ORCID

Affiliation:

1. Translational and Clinical Research Program, Cancer Research Center (IBMCC, CSIC—University of Salamanca), Cytometry Service, NUCLEUS, Department of Medicine, University of Salamanca (Universidad de Salamanca), 37008 Salamanca, Spain

2. Institute of Biomedical Research of Salamanca (IBSAL), 37007 Salamanca, Spain

3. Biomedical Research Networking Centre Consortium of Oncology (CIBERONC), Instituto de Salud Carlos III, 28029 Madrid, Spain

4. Oncohematology Group, Cancer Research Center (IBMCC/CSIC/USAL/IBSAL), 37007 Salamanca, Spain

5. Department of Physiology and Pharmacology, University of Salamanca, 37007 Salamanca, Spain

6. Department of Pharmaceutical Sciences, Organic Chemistry, Faculty of Pharmacy, University of Salamanca, CIETUS, IBSAL, 37007 Salamanca, Spain

7. Proteomics Unit-IBSAL, Instituto de Investigación Biomédica de Salamanca, Universidad de Salamanca, (IBSAL/USAL), 37007 Salamanca, Spain

Abstract

Immunopeptidomics is the area of knowledge focused on the study of peptides assembled in the major histocompatibility complex (MHC), or human leukocyte antigen (HLA) in humans, which could activate the immune response via specific and selective T cell recognition. Advances in high-sensitivity mass spectrometry have enabled the detailed identification and quantification of the immunopeptidome, significantly impacting fields like oncology, infections, and autoimmune diseases. Current immunopeptidomics approaches primarily focus on workflows to identify immunopeptides from HLA molecules, requiring the isolation of the HLA from relevant cells or tissues. Common critical steps in these workflows, such as cell lysis, HLA immunoenrichment, and peptide isolation, significantly influence outcomes. A systematic evaluation of these steps led to the creation of an ‘Immunopeptidome Score’ to enhance the reproducibility and robustness of these workflows. This score, derived from LC-MS/MS datasets (ProteomeXchange identifier PXD038165), in combination with available information from public databases, aids in optimizing the immunopeptidome characterization process. The ‘Immunopeptidome Score’ has been applied in a systematic analysis of protein extraction, HLA immunoprecipitation, and peptide recovery yields across several tumor cell lines enabling the selection of peptides with optimal features and, therefore, the identification of potential biomarker and therapeutic targets.

Publisher

MDPI AG

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