Evidence map›Paper›PMID 36736316›Full record

ArticleMolecular cell2023

Multiplexed kinase interactome profiling quantifies cellular network activity and plasticity.

Martin Golkowski, Andrea Lius, Tanmay Sapre, Ho-Tak Lau, Taylor Moreno, Dustin J Maly, Shao-En Ong

Abstract read
In one paragraph

Article in Molecular cell, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Article
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  9. bioRxiv : the preprint server for biology · 2025
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  18. Review
  19. eLife · 2024
    Article
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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

7 authors.

Martin GolkowskiDepartment of Pharmacology, University of Washington, Seattle, WA 98195, USA. Electronic address: martin.golkowski@utah.edu.
Andrea LiusDepartment of Pharmacology, University of Washington, Seattle, WA 98195, USA.
Tanmay SapreDepartment of Pharmacology, University of Washington, Seattle, WA 98195, USA.
Ho-Tak LauDepartment of Pharmacology, University of Washington, Seattle, WA 98195, USA.
Taylor MorenoDepartment of Pharmacology, University of Washington, Seattle, WA 98195, USA.
Dustin J MalyDepartment of Chemistry, University of Washington, Seattle, WA 98195, USA.
Shao-En OngDepartment of Pharmacology, University of Washington, Seattle, WA 98195, USA. Electronic address: shaoen@uw.edu.

Funding

New Molecular Probes For Protein KinasesR01GM086858 · NIGMS · UNIVERSITY OF WASHINGTON · PI MALY, DUSTIN J · 2008 to 2025
$5.5M
Supplement to DEFINING PATHWAY-SPECIFIC KINASE SIGNALING MODULES WITH PROTEOMICSR01GM129090 · NIGMS · UNIVERSITY OF WASHINGTON · PI ONG, SHAO-EN · 2019 to 2022
$1.7M
A NanoLC-Orbitrap Tribrid Instrument for Comprehensive Proteomics AnalysesS10OD021502 · OD · UNIVERSITY OF WASHINGTON · PI ONG, SHAO-EN · 2017 to 2017
$906k
Targeting understudied kinases in cancer cell plasticity and drug resistanceR03TR003308 · NCATS · UNIVERSITY OF WASHINGTON · PI GOLKOWSKI, MARTIN · 2020 to 2020
$156k
NCATS NIH HHS R03 TR003308NIGMS NIH HHS R01 GM086858NIGMS NIH HHS R01 GM129090NIH HHS S10 OD021502
6 · The paper itself

Abstract

Dynamic changes in protein-protein interaction (PPI) networks underlie all physiological cellular functions and drive devastating human diseases. Profiling PPI networks can, therefore, provide critical insight into disease mechanisms and identify new drug targets. Kinases are regulatory nodes in many PPI networks; yet, facile methods to systematically study kinase interactome dynamics are lacking. We describe kinobead competition and correlation analysis (kiCCA), a quantitative mass spectrometry-based chemoproteomic method for rapid and highly multiplexed profiling of endogenous kinase interactomes. Using kiCCA, we identified 1,154 PPIs of 238 kinases across 18 diverse cancer lines, quantifying context-dependent kinase interactome changes linked to cancer type, plasticity, and signaling states, thereby assembling an extensive knowledgebase for cell signaling research. We discovered drug target candidates, including an endocytic adapter-associated kinase (AAK1) complex that promotes cancer cell epithelial-mesenchymal plasticity and drug resistance. Our data demonstrate the importance of kinase interactome dynamics for cellular signaling in health and disease.

Indexed as

NeoplasmsHumansProtein Interaction MapsSignal Transductionkinomenative complexprotein interactionsproteomicssignaling pathways

Identifiers

PMID36736316
PMCPMC10072906

What Socratic holds

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Registered trials

None linked

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 Socratic graph.