Evidence map›Paper›PMID 40067882›Full record

ArticleJournal of the American Society for Mass Spectrometry2025

TargetSeeker-MS: A Bayesian Inference Approach for Drug-Target Discovery Using Protein Fractionation Coupled to Mass Spectrometry.

Mathieu Lavallée-Adam, Alexander Pelletier, Jolene K Diedrich, Antonio F M Pinto, Salvador Martínez-Bartolomé, Michael Petrascheck, James J Moresco, John R Yates

Abstract read
In one paragraph

Article in Journal of the American Society for Mass Spectrometry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Mathieu Lavallée-AdamDepartment of Molecular Medicine, Scripps Research, 10550 N. Torrey Pines Rd., La Jolla, California 92037, United States.ORCID 0000-0003-2124-3872
Alexander PelletierDepartment of Molecular Medicine, Scripps Research, 10550 N. Torrey Pines Rd., La Jolla, California 92037, United States.
Jolene K DiedrichDepartment of Molecular Medicine, Scripps Research, 10550 N. Torrey Pines Rd., La Jolla, California 92037, United States.ORCID 0000-0001-6489-4558
Antonio F M PintoDepartment of Molecular Medicine, Scripps Research, 10550 N. Torrey Pines Rd., La Jolla, California 92037, United States.ORCID 0000-0002-1573-8011
Salvador Martínez-BartoloméDepartment of Molecular Medicine, Scripps Research, 10550 N. Torrey Pines Rd., La Jolla, California 92037, United States.ORCID 0000-0001-7592-5612
Michael PetrascheckDepartment of Molecular Medicine, Scripps Research, 10550 N. Torrey Pines Rd., La Jolla, California 92037, United States.
James J MorescoDepartment of Molecular Medicine, Scripps Research, 10550 N. Torrey Pines Rd., La Jolla, California 92037, United States.ORCID 0000-0003-1178-1642
John R YatesDepartment of Molecular Medicine, Scripps Research, 10550 N. Torrey Pines Rd., La Jolla, California 92037, United States.ORCID 0000-0001-5267-1672

Funding

TrainingP41GM103533 · NIGMS · UNIVERSITY OF WASHINGTON · PI YATES III, JOHN R · 2012 to 2021
$20.7M
TRAININGU54GM114833 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LINDSEY, MERRY L., PING, PEIPEI · 2014 to 2017
$13.8M
Proteogenetics of Autism Spectrum DisordersR01MH100175 · NIMH · SCRIPPS RESEARCH INSTITUTE, THE · PI MUOTRI, ALYSSON R., YATES III, JOHN R · 2013 to 2025
$7.4M
Quantitative Proteome Analysis of Brain DevelopmentR01MH067880 · NIMH · SCRIPPS RESEARCH INSTITUTE, THE · PI YATES III, JOHN R · 2003 to 2017
$7.1M
NHLBI NIH HHS HHSN268201000035CNIGMS NIH HHS P41 GM103533NIGMS NIH HHS U54 GM114833NIMH NIH HHS R01 MH067880NIMH NIH HHS R01 MH100175
6 · The paper itself

Abstract

To understand the mechanism of action of a drug and assess its clinical usefulness and viability, it is imperative that its affinity for its putative targets is determined. When coupled to mass spectrometry (MS), energetics-based protein separation (EBPS) techniques, such as a thermal shift assay, have shown great potential to identify the targets of a drug on a proteome scale. Nevertheless, the computational analyses assessing the confidence of drug-target predictions made by these methods have remained tightly tied to the protocol under which the data were produced. To identify drug targets in data sets produced using different EBPS-MS techniques, we have developed a novel flexible Bayesian inference approach named TargetSeeker-MS. We showed that TargetSeeker-MS identifies known and novel drug targets in

Indexed as

Drug DiscoveryMass SpectrometryProteinsAnimalsBayes TheoremCaenorhabditis elegansCaenorhabditis elegans ProteinsHEK293 CellsHumansProteomeProteomicsCaenorhabditis elegans ProteinsProteinsProteomeBioinformaticsDrug target discoveryMass spectrometryProteomicsThermal shift assay

Identifiers

PMID40067882
PMCPMC11968059

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.