Deep Learning-Assisted Analysis of Immunopeptidomics Data.

Methods Mol Biol

Computational Mass Spectrometry, TUM School of Life Sciences, Technical University of Munich, Freising, Germany.

Published: April 2024

AI Article Synopsis

  • LC-MS/MS is a key technique for detecting disease-specific HLA, but analyzing HLA peptides is still tricky due to computational challenges compared to standard proteomics.
  • Recent improvements in fragment ion intensity-based matching scores have helped identify more peptides by comparing predicted and actual mass spectra, especially for non-tryptic peptides.
  • This chapter details three advanced procedures using deep learning models, specifically the Universal Spectrum Explorer (USE) and Oktoberfest tools, to enhance the analysis of mass spectrometry data and improve the identification of HLA peptides and neo-epitopes.

Article Abstract

Liquid chromatography-coupled mass spectrometry (LC-MS/MS) is the primary method to obtain direct evidence for the presentation of disease- or patient-specific human leukocyte antigen (HLA). However, compared to the analysis of tryptic peptides in proteomics, the analysis of HLA peptides still poses computational and statistical challenges. Recently, fragment ion intensity-based matching scores assessing the similarity between predicted and observed spectra were shown to substantially increase the number of confidently identified peptides, particularly in use cases where non-tryptic peptides are analyzed. In this chapter, we describe in detail three procedures on how to benefit from state-of-the-art deep learning models to analyze and validate single spectra, single measurements, and multiple measurements in mass spectrometry-based immunopeptidomics. For this, we explain how to use the Universal Spectrum Explorer (USE), online Oktoberfest, and offline Oktoberfest. For intensity-based scoring, Oktoberfest uses fragment ion intensity and retention time predictions from the deep learning framework Prosit, a deep neural network trained on a very large number of synthetic peptides and tandem mass spectra generated within the ProteomeTools project. The examples shown highlight how deep learning-assisted analysis can increase the number of identified HLA peptides, facilitate the discovery of confidently identified neo-epitopes, or provide assistance in the assessment of the presence of cryptic peptides, such as spliced peptides.

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Source
http://dx.doi.org/10.1007/978-1-0716-3646-6_25DOI Listing

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