Prosit-TMT: Deep Learning Boosts Identification of TMT-Labeled Peptides.


Journal

Analytical chemistry
ISSN: 1520-6882
Titre abrégé: Anal Chem
Pays: United States
ID NLM: 0370536

Informations de publication

Date de publication:
24 05 2022
Historique:
pubmed: 14 5 2022
medline: 26 5 2022
entrez: 13 5 2022
Statut: ppublish

Résumé

The prediction of fragment ion intensities and retention time of peptides has gained significant attention over the past few years. However, the progress shown in the accurate prediction of such properties focused primarily on unlabeled peptides. Tandem mass tags (TMT) are chemical peptide labels that are coupled to free amine groups usually after protein digestion to enable the multiplexed analysis of multiple samples in bottom-up mass spectrometry. It is a standard workflow in proteomics ranging from single-cell to high-throughput proteomics. Particularly for TMT, increasing the number of confidently identified spectra is highly desirable as it provides identification and quantification information with every spectrum. Here, we report on the generation of an extensive resource of synthetic TMT-labeled peptides as part of the ProteomeTools project and present the extension of the deep learning model Prosit to accurately predict the retention time and fragment ion intensities of TMT-labeled peptides with high accuracy. Prosit-TMT supports CID and HCD fragmentation and ion trap and Orbitrap mass analyzers in a single model. Reanalysis of published TMT data sets show that this single model extracts substantial additional information. Applying Prosit-TMT, we discovered that the expression of many proteins in human breast milk follows a distinct daily cycle which may prime the newborn for nutritional or environmental cues.

Identifiants

pubmed: 35549156
doi: 10.1021/acs.analchem.1c05435
doi:

Substances chimiques

Peptides 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

7181-7190

Auteurs

Wassim Gabriel (W)

Computational Mass Spectrometry, Technical University of Munich, 85354 Freising, Germany.

Matthew The (M)

Chair of Proteomics and Bioanalytics, Technical University of Munich, 85354 Freising, Germany.

Daniel P Zolg (DP)

Chair of Proteomics and Bioanalytics, Technical University of Munich, 85354 Freising, Germany.

Florian P Bayer (FP)

Chair of Proteomics and Bioanalytics, Technical University of Munich, 85354 Freising, Germany.

Omar Shouman (O)

Computational Mass Spectrometry, Technical University of Munich, 85354 Freising, Germany.

Ludwig Lautenbacher (L)

Computational Mass Spectrometry, Technical University of Munich, 85354 Freising, Germany.

Karsten Schnatbaum (K)

JPT Peptide Technologies GmbH, 12489 Berlin, Germany.

Johannes Zerweck (J)

JPT Peptide Technologies GmbH, 12489 Berlin, Germany.

Tobias Knaute (T)

JPT Peptide Technologies GmbH, 12489 Berlin, Germany.

Bernard Delanghe (B)

Thermo Fisher Scientific, 28199 Bremen, Germany.

Andreas Huhmer (A)

Thermo Fisher Scientific, San Jose, California 95134, United States.

Holger Wenschuh (H)

JPT Peptide Technologies GmbH, 12489 Berlin, Germany.

Ulf Reimer (U)

JPT Peptide Technologies GmbH, 12489 Berlin, Germany.

Guillaume Médard (G)

Chair of Proteomics and Bioanalytics, Technical University of Munich, 85354 Freising, Germany.

Bernhard Kuster (B)

Chair of Proteomics and Bioanalytics, Technical University of Munich, 85354 Freising, Germany.
Bavarian Center for Biomolecular Mass Spectrometry, 85354 Freising, Germany.

Mathias Wilhelm (M)

Computational Mass Spectrometry, Technical University of Munich, 85354 Freising, Germany.

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Classifications MeSH