Evidence map›Paper›PMID 30265007›Full record

ArticleJournal of proteome research2018

d2ome, Software for in Vivo Protein Turnover Analysis Using Heavy Water Labeling and LC-MS, Reveals Alterations of Hepatic Proteome Dynamics in a Mouse Model of NAFLD.

Rovshan G Sadygov, Jayant Avva, Mahbubur Rahman, Kwangwon Lee, Sergei Ilchenko, Takhar Kasumov, Ahmad Borzou

Erratum issuedAbstract read
In one paragraph

Article in Journal of proteome research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing 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

39 citing papers in PubMed.

  1. Kinetic Lipidomics: QuantifyingbioRxiv : the preprint server for biology · 2026
    Article
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  3. Resilience of the mitochondrial reticulum in aging.American journal of physiology. Endocrinology and metabolism · 2025
    Article
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  10. Metabolomic and proteomic applications to exercise biomedicine.Translational exercise biomedicine · 2024
    Review
  11. Flexible Quality Control for Protein Turnover Rates Using d2ome.International journal of molecular sciences · 2023
    Article
  12. Article
  13. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Rovshan G SadygovDepartment of Biochemistry and Molecular Biology, Sealy Center for Molecular Medicine , The University of Texas Medical Branch , 301 University Blvd. , Galveston , Texas 77555 , United States.ORCID 0000-0003-1590-155X
Jayant AvvaDepartment of Biochemistry and Molecular Biology, Sealy Center for Molecular Medicine , The University of Texas Medical Branch , 301 University Blvd. , Galveston , Texas 77555 , United States.
Mahbubur RahmanDepartment of Biochemistry and Molecular Biology, Sealy Center for Molecular Medicine , The University of Texas Medical Branch , 301 University Blvd. , Galveston , Texas 77555 , United States.
Kwangwon LeeDepartment of Pharmaceutical Sciences , Northeast Ohio Medical University , Rootstown , Ohio 44272 , United States.
Sergei IlchenkoDepartment of Pharmaceutical Sciences , Northeast Ohio Medical University , Rootstown , Ohio 44272 , United States.
Takhar KasumovDepartment of Pharmaceutical Sciences , Northeast Ohio Medical University , Rootstown , Ohio 44272 , United States.
Ahmad BorzouDepartment of Biochemistry and Molecular Biology, Sealy Center for Molecular Medicine , The University of Texas Medical Branch , 301 University Blvd. , Galveston , Texas 77555 , United States.

Funding

Novel computational methods for in vivo proteome dynamics estimation using heavy water metabolic labeling and LC-MSR01GM112044 · NIGMS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI SADYGOV, ROVSHAN G · 2015 to 2023
$2.7M
NIGMS NIH HHS R01 GM112044
6 · The paper itself

Abstract

Metabolic labeling with heavy water followed by LC-MS is a high throughput approach to study proteostasis in vivo. Advances in mass spectrometry and sample processing have allowed consistent detection of thousands of proteins at multiple time points. However, freely available automated bioinformatics tools to analyze and extract protein decay rate constants are lacking. Here, we describe d2ome-a robust, automated software solution for in vivo protein turnover analysis. d2ome is highly scalable, uses innovative approaches to nonlinear fitting, implements Grubbs' outlier detection and removal, uses weighted-averaging of replicates, applies a data dependent elution time windowing, and uses mass accuracy in peak detection. Here, we discuss the application of d2ome in a comparative study of protein turnover in the livers of normal vs Western diet-fed LDLR

Indexed as

SoftwareAnimalsChromatography, LiquidDeuterium OxideDiet, WesternDisease Models, AnimalGene ExpressionHalf-LifeIsotope LabelingLiverMiceMice, Inbred C57BLMice, KnockoutNon-alcoholic Fatty Liver DiseaseProtein Interaction MappingProteolysisDeuterium OxideProteomeReceptors, LDLRibosomal Proteinsin vivo protein turnovermetabolic labelingNAFLDnonlinear least-squares modelingpeak detection and integrationprotein half-life; UPR; 40S ribosomal proteins; isotopomer quantificationproteome dynamics

Identifiers

PMID30265007
PMCPMC6466633

What OpenQuestion holds

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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 OpenQuestion graph.