Evidence map›Paper›PMID 26979493›Full record

ArticleJournal of proteome research2016

Extraction, Enrichment, Solubilization, and Digestion Techniques for Membrane Proteomics.

Stephanie M Moore, Stephanie M Hess, James W Jorgenson

Abstract read
In one paragraph

Article in Journal of proteome research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Top-down proteomics.Nature reviews. Methods primers · 2024
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Strategies for Rapid Identification ofFrontiers in cellular and infection microbiology · 2021
    Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Top-Down Proteomics: Ready for Prime Time?Analytical chemistry · 2018
    Review
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

3 authors.

Stephanie M MooreChemistry Department University of North Carolina at Chapel Hill , Chapel Hill, North Carolina 27599, United States.
Stephanie M HessChemistry Department University of North Carolina at Chapel Hill , Chapel Hill, North Carolina 27599, United States.
James W JorgensonChemistry Department University of North Carolina at Chapel Hill , Chapel Hill, North Carolina 27599, United States.

Funding

Statistics and Bioinformatics Core - WangU24DK097153 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BURANT, CHARLES F · 2012 to 2017
$10.1M
High Resolution MetabolomicsR01DK101473 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KENNEDY, ROBERT T · 2015 to 2018
$1000k
NIDDK NIH HHS 1R01DK101473-01A1NIDDK NIH HHS 5U24DK097153NIDDK NIH HHS R01 DK101473NIDDK NIH HHS U24 DK097153
6 · The paper itself

Abstract

The importance of membrane proteins in biological systems is indisputable; however, their amphipathic nature makes them difficult to analyze. In this study, the most popular techniques for extraction, enrichment, solubilization, and digestion are compared, resulting in an overall improved workflow for the insoluble portion of Saccharomyces cerevisiae cell lysate. Yeast cells were successfully lysed using a French press pressure cell at 20 000 psi, and resulting proteins were fractionated prior to digestion to reduce sample complexity. The proteins were best solubilized with the addition of ionic detergent sodium deoxycholate (1%) and through the application of high-frequency sonication prior to a tryptic digestion at 37 °C. Overall, the improved membrane proteomic workflow resulted in a 26% increase in membrane protein identifications for baker's yeast. In addition, more membrane protein identifications were unique to the improved protocol. When comparing membrane proteins that were identified in the improved protocol and the standard operating procedure (176 proteins), 93% of these proteins were present in greater abundance (higher intensity) when using the improved method.

Indexed as

Chromatography, LiquidComplex MixturesDeoxycholic AcidDetergentsMass SpectrometryMembrane ProteinsPressureProteolysisSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSolubilitySonicationTrypsinComplex MixturesDeoxycholic AcidDetergentsMembrane ProteinsSaccharomyces cerevisiae ProteinsTrypsinmembrane proteinsSaccharomyces cerevisiaesample preparation techniquessodium deoxycholatesonication

Identifiers

PMID26979493
PMCPMC5488330

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.