Evidence map›Paper›PMID 20514218›Full record

ArticleCurrent genomics2009

Getting a grip on complexes.

Yan Nie, Cristina Viola, Christoph Bieniossek, Simon Trowitzsch, Lakshmi Sumitra Vijay-Achandran, Maxime Chaillet, Frederic Garzoni, Imre Berger

Open access · bronzeAbstract read
In one paragraph

Article in Current genomics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. VLP-factory™ and ADDomerCurrent protocols · 2021
    Article
  3. Review
  4. Article
  5. Review
  6. Protein Complex Affinity Capture from Cryomilled Mammalian Cells.Journal of visualized experiments : JoVE · 2016
    Article
  7. Review
  8. Article
  9. Multiprotein complex production in insect cells by using polyproteins.Methods in molecular biology (Clifton, N.J.) · 2014
    Article
  10. The multiBac protein complex production platform at the EMBL.Journal of visualized experiments : JoVE · 2013
    Article
  11. Review
  12. Article
  13. Review
  14. 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

8 authors at 4 institutions in 1 country.

Yan NieEuropean Molecular Biology Laboratory (EMBL), Grenoble Outstation and Unit of Virus Host-Cell Interactions (UVHCI), UJF-EMBL-CNRS, UMR 5233, 6 rue Jules Horowitz, 38042 Grenoble CEDEX 9, France.
Cristina Viola
Christoph Bieniossek
Simon Trowitzsch
Lakshmi Sumitra Vijay-Achandran
Maxime Chaillet
Frederic Garzoni
Imre Berger
Centre National de la Recherche Scientifique · FRUnit of Virus Host Cell Interactions · FRUniversité Joseph Fourier · FREuropean Molecular Biology Laboratory · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We are witnessing tremendous advances in our understanding of the organization of life. Complete genomes are being deciphered with ever increasing speed and accuracy, thereby setting the stage for addressing the entire gene product repertoire of cells, towards understanding whole biological systems. Advances in bioinformatics and mass spectrometric techniques have revealed the multitude of interactions present in the proteome. Multiprotein complexes are emerging as a paramount cornerstone of biological activity, as many proteins appear to participate, stably or transiently, in large multisubunit assemblies. Analysis of the architecture of these assemblies and their manifold interactions is imperative for understanding their function at the molecular level. Structural genomics efforts have fostered the development of many technologies towards achieving the throughput required for studying system-wide single proteins and small interaction motifs at high resolution. The present shift in focus towards large multiprotein complexes, in particular in eukaryotes, now calls for a likewise concerted effort to develop and provide new technologies that are urgently required to produce in quality and quantity the plethora of multiprotein assemblies that form the complexome, and to routinely study their structure and function at the molecular level. Current efforts towards this objective are summarized and reviewed in this contribution.

Indexed as

ACEMBLBEVScomplexomics.interactomemultiBacmultigene expressionmultiprotein assembliesProteomeroboticsstructural genomics

Identifiers

PMID20514218
PMCPMC2817887
OpenAlexW2091963860

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.