Evidence map›Paper›PMID 25165137›Full record

ArticleMolecular biology of the cell2014

Fractionation profiling: a fast and versatile approach for mapping vesicle proteomes and protein-protein interactions.

Georg H H Borner, Marco Y Hein, Jennifer Hirst, James R Edgar, Matthias Mann, Margaret S Robinson

Open access · greenAbstract readValidation Study
In one paragraph

Article in Molecular biology of the cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

33 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. Article
  3. FGFR3 drives Aβ-induced tau uptake.Experimental & molecular medicine · 2024
    Article
  4. Article
  5. Article
  6. PSL-LCCL: a resource for subcellular protein localization in liver cancer cell line SK_HEP1.Database : the journal of biological databases and curation · 2022
    Article
  7. Article
  8. Subcellular proteomics.Nature reviews. Methods primers · 2021
    Article
  9. Article
  10. Organellar Maps Through Proteomic Profiling - A Conceptual Guide.Molecular & cellular proteomics : MCP · 2020
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Spatial proteomics: a powerful discovery tool for cell biology.Nature reviews. Molecular cell biology · 2019
    Review
  17. 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

6 authors at 2 institutions in 2 countries.

Georg H H BornerDepartment of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany borner@biochem.mpg.de.
Marco Y HeinDepartment of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany.
Jennifer HirstCambridge Institute for Medical Research, University of Cambridge, Cambridge CB2 0XY, United Kingdom.
James R EdgarCambridge Institute for Medical Research, University of Cambridge, Cambridge CB2 0XY, United Kingdom.
Matthias MannDepartment of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany.
Margaret S RobinsonCambridge Institute for Medical Research, University of Cambridge, Cambridge CB2 0XY, United Kingdom.
Max Planck Institute of Biochemistry · DEUniversity of Cambridge · GB

Funding

Wellcome Trust 086598Wellcome Trust 100140Wellcome Trust RG52996
6 · The paper itself

Abstract

We developed "fractionation profiling," a method for rapid proteomic analysis of membrane vesicles and protein particles. The approach combines quantitative proteomics with subcellular fractionation to generate signature protein abundance distribution profiles. Functionally associated groups of proteins are revealed through cluster analysis. To validate the method, we first profiled >3500 proteins from HeLa cells and identified known clathrin-coated vesicle proteins with >90% accuracy. We then profiled >2400 proteins from Drosophila S2 cells, and we report the first comprehensive insect clathrin-coated vesicle proteome. Of importance, the cluster analysis extends to all profiled proteins and thus identifies a diverse range of known and novel cytosolic and membrane-associated protein complexes. We show that it also allows the detailed compositional characterization of complexes, including the delineation of subcomplexes and subunit stoichiometry. Our predictions are presented in an interactive database. Fractionation profiling is a universal method for defining the clathrin-coated vesicle proteome and may be adapted for the analysis of other types of vesicles and particles. In addition, it provides a versatile tool for the rapid generation of large-scale protein interaction maps.

Indexed as

Adaptor Proteins, Vesicular TransportAnimalsCell FractionationClathrin-Coated VesiclesDrosophilaHeLa CellsHumansMembrane ProteinsProtein Interaction MappingProteomeAdaptor Proteins, Vesicular TransportMembrane ProteinsProteome

Identifiers

PMID25165137
PMCPMC4196868
OpenAlexW2153328834

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.