Evidence map›Paper›PMID 24040290›Full record

ArticlePloS one2013

Stepwise assembly of fibrinogen is assisted by the endoplasmic reticulum lectin-chaperone system in HepG2 cells.

Taku Tamura, Seisuke Arai, Hisao Nagaya, Jun Mizuguchi, Ikuo Wada

Open access · goldAbstract read
In one paragraph

Article in PloS one, 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
0.5field-weighted citation impact, top 29% 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, 16 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Turnover of EDEM1, an ERAD-enhancing factor, is mediated by multiple degradation routes.Genes to cells : devoted to molecular & cellular mechanisms · 2024
    Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. PDI Family Members as Guides for Client Folding and Assembly.International journal of molecular sciences · 2020
    Review
  10. Hereditary Hypofibrinogenemia with Hepatic Storage.International journal of molecular sciences · 2020
    Review
  11. Article
  12. Fibrin Formation, Structure and Properties.Sub-cellular biochemistry · 2017
    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

5 authors at 3 institutions in 1 country.

Taku TamuraDepartment of Cell Science, Institute of Biomedical Sciences, Fukushima Medical University, Fukushima, Japan ; Core Research for Evolutional Science and Technology, Japan Science and Technology Agency (JST), Tokyo, Japan.
Seisuke Arai
Hisao Nagaya
Jun Mizuguchi
Ikuo Wada
Fukushima Medical University · JPJapan Science and Technology Agency · JPKaketsuken (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The endoplasmic reticulum (ER) plays essential roles in protein folding and assembly of secretory proteins. ER-resident molecular chaperones and related enzymes assist in protein maturation by co-operated interactions and modifications. However, the folding/assembly of multimeric proteins is not well understood. Here, we show that the maturation of fibrinogen, a hexameric secretory protein (two trimers from α, β and γ subunits), occurs in a stepwise manner. The αγ complex, a precursor for the trimer, is retained in the ER by lectin-like chaperones, and the β subunit is incorporated into the αγ complex immediately after translation. ERp57, a protein disulfide isomerase homologue, is involved in the hexamer formation from two trimers. Our results indicate that the fibrinogen hexamer is formed sequentially, rather than simultaneously, using kinetic pause by lectin chaperones. This study provides a novel insight into the assembly of most abundant multi-subunit secretory proteins.

Indexed as

Endoplasmic ReticulumFibrinogenGenes, ReporterGreen Fluorescent ProteinsHep G2 CellsHumansKineticsMolecular ChaperonesProtein BiosynthesisProtein Disulfide-IsomerasesProtein FoldingProtein MultimerizationProtein SubunitsRNA, Small InterferingCyan Fluorescent ProteinFibrinogenGreen Fluorescent ProteinsMolecular ChaperonesPDIA3 protein, humanProtein Disulfide-IsomerasesProtein SubunitsRNA, Small Interfering

Identifiers

PMID24040290
PMCPMC3769264
OpenAlexW2071203988

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.