Evidence map›Paper›PMID 26399295›Full record

ArticleMolecular biology of the cell2015

Proteome-wide quantitative multiplexed profiling of protein expression: carbon-source dependency in Saccharomyces cerevisiae.

Joao A Paulo, Jeremy D O'Connell, Aleksandr Gaun, Steven P Gygi

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing 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

36 citing papers in PubMed.

  1. Article
  2. Article
  3. RewiringMetabolic engineering communications · 2024
    Article
  4. Article
  5. The regulatory landscape of the yeast phosphoproteome.Nature structural & molecular biology · 2023
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Pectinases Secretion byMolecules (Basel, Switzerland) · 2022
    Article
  13. Article
  14. Molecular and cellular biology · 2021
    Article
  15. In vitro turnover numbers do not reflect in vivo activities of yeast enzymes.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  16. Review
  17. A yeast FRET biosensor enlightens cAMP signaling.Molecular biology of the cell · 2021
    Article
  18. Article
  19. Article
  20. Article
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

4 authors.

Joao A PauloDepartment of Cell Biology, Harvard Medical School, Boston, MA 02115 joao_paulo@hms.harvard.edu sgygi@hms.harvard.edu.
Jeremy D O'ConnellDepartment of Cell Biology, Harvard Medical School, Boston, MA 02115.
Aleksandr GaunDepartment of Cell Biology, Harvard Medical School, Boston, MA 02115.
Steven P GygiDepartment of Cell Biology, Harvard Medical School, Boston, MA 02115 joao_paulo@hms.harvard.edu sgygi@hms.harvard.edu.

Funding

Resolving the role of nicotine-mediated phosphorylation on pancreatic fibrosisK01DK098285 · NIDDK · HARVARD MEDICAL SCHOOL · PI PAULO, JOAO A · 2013 to 2017
$638k
NIDDK NIH HHS K01 DK098285NIGMS NIH HHS GM97645
6 · The paper itself

Abstract

The global proteomic alterations in the budding yeast Saccharomyces cerevisiae due to differences in carbon sources can be comprehensively examined using mass spectrometry-based multiplexing strategies. In this study, we investigate changes in the S. cerevisiae proteome resulting from cultures grown in minimal media using galactose, glucose, or raffinose as the carbon source. We used a tandem mass tag 9-plex strategy to determine alterations in relative protein abundance due to a particular carbon source, in triplicate, thereby permitting subsequent statistical analyses. We quantified more than 4700 proteins across all nine samples; 1003 proteins demonstrated statistically significant differences in abundance in at least one condition. The majority of altered proteins were classified as functioning in metabolic processes and as having cellular origins of plasma membrane and mitochondria. In contrast, proteins remaining relatively unchanged in abundance included those having nucleic acid-related processes, such as transcription and RNA processing. In addition, the comprehensiveness of the data set enabled the analysis of subsets of functionally related proteins, such as phosphatases, kinases, and transcription factors. As a resource, these data can be mined further in efforts to understand better the roles of carbon source fermentation in yeast metabolic pathways and the alterations observed therein, potentially for industrial applications, such as biofuel feedstock production.

Indexed as

CarbonFermentationGalactoseGene Expression Regulation, FungalGlucoseMass SpectrometryMitochondriaProtein Processing, Post-TranslationalProteomeProteomicsRaffinoseSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSaccharomycetalesTranscription FactorsCarbonGalactoseGlucoseProteomeRaffinoseSaccharomyces cerevisiae ProteinsTranscription Factors

Identifiers

PMID26399295
PMCPMC4710237

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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 OpenQuestion graph.