Computational Tools for the Identification and Interpretation of Sequence Motifs in Immunopeptidomes. Issue 12 (26th February 2018)

• Record Type: Journal Article
• Authors: Alvarez, Bruno; Barra, Carolina; Nielsen, Morten; Andreatta, Massimo
• Other Names: Ternette Nicola guestEditor.; Purcell Anthony W. guestEditor.
• Is Part Of: Proteomics. Volume 18:Issue 12(2018)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2018-02-26
• Subjects: GibbsCluster -- mass spectrometry -- MHC -- prediction models -- sequence motifs; Proteins -- Separation -- Periodicals; Bioinformatics -- Periodicals; Proteomics -- Periodicals; Genomes -- Periodicals; Molecular genetics -- Periodicals; 572.605
• DOI: 10.1002/pmic.201700252
• Languages: English
• ISSNs: 1615-9853

Abstract

Abstract: Recent advances in proteomics and mass‐spectrometry have widely expanded the detectable peptide repertoire presented by major histocompatibility complex (MHC) molecules on the cell surface, collectively known as the immunopeptidome. Finely characterizing the immunopeptidome brings about important basic insights into the mechanisms of antigen presentation, but can also reveal promising targets for vaccine development and cancer immunotherapy. This report describes a number of practical and efficient approaches to analyze immunopeptidomics data, discussing the identification of meaningful sequence motifs in various scenarios and considering current limitations. Guidelines are provided for the filtering of false hits and contaminants, and to address the problem of motif deconvolution in cell lines expressing multiple MHC alleles, both for the MHC class I and class II systems. Finally, it is demonstrated how machine learning can be readily employed by non‐expert users to generate accurate prediction models directly from mass‐spectrometry eluted ligand data sets.