AI-Assisted Processing Pipeline to Boost Protein Isoform Detection.

Methods Mol Biol

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

Published: July 2024

AI Article Synopsis

  • Proteomics is the study of proteins, and it's getting better at finding different versions of proteins called isoforms.
  • A challenge in this area is figuring out how to accurately identify these isoforms because there's a lot of data to sort through.
  • New tools using artificial intelligence can help scientists search for and identify proteins more effectively, leading to more discoveries about how proteins work in living things.

Article Abstract

Proteomics, the study of proteins within biological systems, has seen remarkable advancements in recent years, with protein isoform detection emerging as one of the next major frontiers. One of the primary challenges is achieving the necessary peptide and protein coverage to confidently differentiate isoforms as a result of the protein inference problem and protein false discovery rate estimation challenge in large data. In this chapter, we describe the application of artificial intelligence-assisted peptide property prediction for database search engine rescoring by Oktoberfest, an approach that has proven effective, particularly for complex samples and extensive search spaces, which can greatly increase peptide coverage. Further, it illustrates a method for increasing isoform coverage by the PickedGroupFDR approach that is designed to excel when applied on large data. Real-world examples are provided to illustrate the utility of the tools in the context of rescoring, protein grouping, and false discovery rate estimation. By implementing these cutting-edge techniques, researchers can achieve a substantial increase in both peptide and isoform coverage, thus unlocking the potential of protein isoform detection in their studies and shedding light on their roles and functions in biological processes.

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Source
http://dx.doi.org/10.1007/978-1-0716-4007-4_10DOI Listing

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