| Literature DB >> 31133760 |
Siegfried Gessulat1,2, Tobias Schmidt1, Daniel Paul Zolg1, Patroklos Samaras1, Karsten Schnatbaum3, Johannes Zerweck3, Tobias Knaute3, Julia Rechenberger1, Bernard Delanghe4, Andreas Huhmer5, Ulf Reimer3, Hans-Christian Ehrlich2, Stephan Aiche2, Bernhard Kuster6,7, Mathias Wilhelm8.
Abstract
In mass-spectrometry-based proteomics, the identification and quantification of peptides and proteins heavily rely on sequence database searching or spectral library matching. The lack of accurate predictive models for fragment ion intensities impairs the realization of the full potential of these approaches. Here, we extended the ProteomeTools synthetic peptide library to 550,000 tryptic peptides and 21 million high-quality tandem mass spectra. We trained a deep neural network, termed Prosit, resulting in chromatographic retention time and fragment ion intensity predictions that exceed the quality of the experimental data. Integrating Prosit into database search pipelines led to more identifications at >10× lower false discovery rates. We show the general applicability of Prosit by predicting spectra for proteases other than trypsin, generating spectral libraries for data-independent acquisition and improving the analysis of metaproteomes. Prosit is integrated into ProteomicsDB, allowing search result re-scoring and custom spectral library generation for any organism on the basis of peptide sequence alone.Entities:
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Year: 2019 PMID: 31133760 DOI: 10.1038/s41592-019-0426-7
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547