Evidence map›Paper›PMID 40645189›Full record

ArticleCell reports methods2025

Deuterium labeling enables proteome-wide turnover kinetics analysis in cell culture.

Lorena Alamillo, Dominic C M Ng, Jordan Currie, Alexander Black, Boomathi Pandi, Vyshnavi Manda, Jay Pavelka, Peyton Schaal, Joshua G Travers, Timothy A McKinsey and 2 more

Abstract read
In one paragraph

Article in Cell reports methods, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Kinetic Lipidomics: QuantifyingbioRxiv : the preprint server for biology · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Lorena AlamilloDepartment of Medicine, Division of Cardiology, University of Colorado School of Medicine, Aurora, CO, USA; Consortium for Fibrosis Research & Translation, University of Colorado School of Medicine, Aurora, CO, USA.
Dominic C M NgDepartment of Medicine, Division of Cardiology, University of Colorado School of Medicine, Aurora, CO, USA; Consortium for Fibrosis Research & Translation, University of Colorado School of Medicine, Aurora, CO, USA.
Jordan CurrieDepartment of Medicine, Division of Cardiology, University of Colorado School of Medicine, Aurora, CO, USA; Consortium for Fibrosis Research & Translation, University of Colorado School of Medicine, Aurora, CO, USA.
Alexander BlackDepartment of Medicine, Division of Cardiology, University of Colorado School of Medicine, Aurora, CO, USA; Consortium for Fibrosis Research & Translation, University of Colorado School of Medicine, Aurora, CO, USA.
Boomathi PandiDepartment of Medicine, Division of Cardiology, University of Colorado School of Medicine, Aurora, CO, USA; Consortium for Fibrosis Research & Translation, University of Colorado School of Medicine, Aurora, CO, USA.
Vyshnavi MandaDepartment of Medicine, Division of Cardiology, University of Colorado School of Medicine, Aurora, CO, USA; Consortium for Fibrosis Research & Translation, University of Colorado School of Medicine, Aurora, CO, USA.
Jay PavelkaDepartment of Medicine, Division of Cardiology, University of Colorado School of Medicine, Aurora, CO, USA; Consortium for Fibrosis Research & Translation, University of Colorado School of Medicine, Aurora, CO, USA.
Peyton SchaalDepartment of Medicine, Division of Cardiology, University of Colorado School of Medicine, Aurora, CO, USA; Consortium for Fibrosis Research & Translation, University of Colorado School of Medicine, Aurora, CO, USA.
Joshua G TraversDepartment of Medicine, Division of Cardiology, University of Colorado School of Medicine, Aurora, CO, USA; Consortium for Fibrosis Research & Translation, University of Colorado School of Medicine, Aurora, CO, USA.
Timothy A McKinseyDepartment of Medicine, Division of Cardiology, University of Colorado School of Medicine, Aurora, CO, USA; Consortium for Fibrosis Research & Translation, University of Colorado School of Medicine, Aurora, CO, USA.
Maggie P Y LamDepartment of Medicine, Division of Cardiology, University of Colorado School of Medicine, Aurora, CO, USA; Consortium for Fibrosis Research & Translation, University of Colorado School of Medicine, Aurora, CO, USA; Department of Biochemistry and Molecular Genetics, University of Colorado School of Medicine, Aurora, CO, USA. Electronic address: maggie.lam@cuanschutz.edu.
Edward LauDepartment of Medicine, Division of Cardiology, University of Colorado School of Medicine, Aurora, CO, USA; Consortium for Fibrosis Research & Translation, University of Colorado School of Medicine, Aurora, CO, USA. Electronic address: edward.lau@cuanschutz.edu.

Funding

Cellular and Molecular Biology at MichiganT32GM145470 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI John Chadwick Brenner · 2022 to 2026
$4.1M
Alternative Protein Isoforms in Ventricular RemodelingR01HL141278 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI Maggie Lam · 2018 to 2026
$3.5M
Post-transcriptional regulations of proteomes in stress and senescenceR01GM144456 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI LAM, MAGGIE · 2022 to 2025
$2.2M
Investigations of Proteome Turnover Kinetics Under Cellular DifferentiationR35GM146815 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI Edward Lau · 2022 to 2026
$2.1M
15-PGDH-Mediated Eicosanoid Degradation in Cardiac Fibrosis and Heart FailureR01HL171711 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI Timothy McKinsey · 2024 to 2026
$1.6M
Multi-Omics Approach to Identify Cardiokines in Human iPSC ModelsR00HL144829 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI LAU, EDWARD · 2020 to 2022
$733k
Elucidating the Molecular Mechanisms and Cellular Specificity of HDAC Inhibitor Efficacy in Diastolic DysfunctionK99HL166708 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI TRAVERS, JOSHUA · 2023 to 2024
$214k
NHLBI NIH HHS K99 HL166708NHLBI NIH HHS R00 HL144829NHLBI NIH HHS R01 HL141278NHLBI NIH HHS R01 HL171711NIGMS NIH HHS R01 GM144456NIGMS NIH HHS R35 GM146815NIGMS NIH HHS T32 GM145470
6 · The paper itself

Abstract

Protein turnover is a critical component of gene expression regulation and cellular homeostasis, yet methods for measuring turnover rates that are scalable and applicable to different models are still needed. We introduce an improved D

Indexed as

Cell Culture TechniquesDeuteriumProteomeProteomicsCell DifferentiationCells, CulturedFibroblastsHumansInduced Pluripotent Stem CellsKineticsMyocytes, CardiacDeuteriumProteomeCP: molecular biologyCP: systems biologydegronheavy waterhiPSCmass spectrometryprotein synthesisprotein turnoversecretometurnover kinetics

Identifiers

PMID40645189
PMCPMC12296481

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.