Evidence map›Paper›PMID 23349476›Full record

ArticleMolecular & cellular proteomics : MCP2013

Global analysis of condition-specific subcellular protein distribution and abundance.

Sunhee Jung, Jennifer J Smith, Priska D von Haller, David J Dilworth, Katherine A Sitko, Leslie R Miller, Ramsey A Saleem, David R Goodlett, John D Aitchison

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.4field-weighted citation impact, top 12% of its field
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

12 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. The interactome challenge.The Journal of cell biology · 2015
    Article
  8. Article
  9. Article
  10. Systems cell biology.The Journal of cell biology · 2014
    Review
  11. Review
  12. Peroxisomes take shape.Nature reviews. Molecular cell biology · 2013
    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

9 authors at 3 institutions in 1 country.

Sunhee JungMolecular and Cellular Biology Program, University of Washington, Seattle, Washington 98195, USA.
Jennifer J Smith
Priska D von Haller
David J Dilworth
Katherine A Sitko
Leslie R Miller
Ramsey A Saleem
David R Goodlett
John D Aitchison
Institute for Systems Biology · USUniversity of Washington · USCenter for Infectious Disease Research · US

Funding

Quantitative Systems BiologyP50GM076547 · NIGMS · INSTITUTE FOR SYSTEMS BIOLOGY · PI BALIGA, NITIN S · 2006 to 2016
$30.6M
NEW TOOLS FOR EXPLORING THE DYNAMIC INTERACTOME(RMI)U54RR022220 · NCRR · ROCKEFELLER UNIVERSITY · PI ROUT, MICHAEL P · 2005 to 2011
$19.3M
Oleate-responsive gene regulatory networks governing peroxisome proliferationR01GM075152 · NIGMS · SEATTLE BIOMEDICAL RESEARCH INSTITUTE · PI AITCHISON, JOHN D. · 2008 to 2011
$1.9M
Parallel Peptide Tandem Mass Spectrometry (MS)R33CA099139 · NCI · UNIVERSITY OF WASHINGTON · PI GOODLETT, DAVID ROBINSON · 2004 to 2009
$1.7M
MULTI-TIERED PROTEOMIC COMPUTE CLUSTER: PARKINSON'S DISEASES10RR023044 · NCRR · UNIVERSITY OF WASHINGTON · PI GOODLETT, DAVID ROBINSON · 2006 to 2006
$500k
NCI NIH HHS 3R33CA099139-04S1NCI NIH HHS 5R33CA099139-04NCI NIH HHS R33 CA099139NCRR NIH HHS 1S10RR023044-01NCRR NIH HHS S10 RR023044NCRR NIH HHS U54 RR022220NCRR NIH HHS U54-RR022220NIGMS NIH HHS P50 GM076547NIGMS NIH HHS P50-GM076547NIGMS NIH HHS R01 GM075152NIGMS NIH HHS R01-GM075152
6 · The paper itself

Abstract

Cellular control of protein activities by modulation of their abundance or compartmentalization is not easily measured on a large scale. We developed and applied a method to globally interrogate these processes that is widely useful for systems-level analyses of dynamic cellular responses in many cell types. The approach involves subcellular fractionation followed by comprehensive proteomic analysis of the fractions, which is enabled by a data-independent acquisition mass spectrometry approach that samples every available mass to charge channel systematically to maximize sensitivity. Next, various fraction-enrichment ratios are measured for all detected proteins across different environmental conditions and used to group proteins into clusters reflecting changes in compartmentalization and relative conditional abundance. Application of the approach to characterize the response of yeast proteins to fatty acid exposure revealed dynamics of peroxisomes and novel dynamics of MCC/eisosomes, specialized plasma membrane domains comprised of membrane compartment occupied by Can1 (MCC) and eisosome subdomains. It also led to the identification of Fat3, a fatty acid transport protein of the plasma membrane, previously annotated as Ykl187.

Indexed as

Cell FractionationCulture MediaGlucoseLipid MetabolismMicroscopy, FluorescenceMolecular Sequence AnnotationOleic AcidOrganellesProtein TransportProteomeProteomicsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSubcellular FractionsCulture MediaGlucoseOleic AcidProteomeSaccharomyces cerevisiae Proteins

Identifiers

PMID23349476
PMCPMC3650349
OpenAlexW2143493486

What OpenQuestion holds

Textmetadata
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.