Evidence map›Paper›PMID 23419775›Full record

ReviewBiochimica et biophysica acta2013

Vesicle-mediated export from the ER: COPII coat function and regulation.

Jennifer G D'Arcangelo, Kyle R Stahmer, Elizabeth A Miller

Open access · greenAbstract readReview
In one paragraph

Review in Biochimica et biophysica acta, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 100 papers.

0numbers the graph read from it
0cells of the map it votes in
100citing papers in PubMed
8.2field-weighted citation impact, top 2% 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

100 citing papers in PubMed, 153 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Trafficking of the human NaProtein science : a publication of the Protein Society · 2026
    Article
  7. Review
  8. Collagen IV biosynthesis: Intracellular choreography of post-translational modifications.Matrix biology : journal of the International Society for Matrix Biology · 2025
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Rare genetic variants inmedRxiv : the preprint server for health sciences · 2023
    Article
  20. Review

40 more citing papers are in PubMed but not listed here.

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 at 1 institution in 1 country.

Jennifer G D'ArcangeloDepartment of Biological Sciences, Columbia University, New York, NY, USA.
Kyle R Stahmer
Elizabeth A Miller
Columbia University · US

Funding

ER export and the quality control checkpoint during membrane protein biogenesisR01GM078186 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI BULINSKI, JEANNETTE CHLOE, MILLER, ELIZABETH A. · 2006 to 2015
$2.7M
Molecular mechanisms of cargo capture into ER-derived transport vesiclesR01GM085089 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI BULINSKI, JEANNETTE CHLOE, MILLER, ELIZABETH A. · 2008 to 2016
$2.4M
NIGMS NIH HHS R01 GM078186NIGMS NIH HHS R01GM078186NIGMS NIH HHS R01 GM085089NIGMS NIH HHS R01GM085089
6 · The paper itself

Abstract

Vesicle trafficking from the endoplasmic reticulum (ER) is a vital cellular process in all eukaryotes responsible for moving secretory cargoes from the ER to the Golgi apparatus. To accomplish this feat, the cell employs a set of conserved cytoplasmic coat proteins - the coat protein II (COPII) complex - that recruit cargo into nascent buds and deform the ER membrane to drive vesicle formation. While our understanding of COPII coat mechanics has developed substantially since its discovery, we have only recently begun to appreciate the factors that regulate this complex and, in turn, ER-to-Golgi trafficking. Here, we describe these factors and their influences on COPII vesicle formation. Properties intrinsic to the GTP cycle of the coat, as well as coat structure, have critical implications for COPII vesicle trafficking. Extrinsic factors in the cytosol can modulate COPII activity through direct interaction with the coat or with scaffolding components, or by changing composition of the ER membrane. Further, lumenal and membrane-bound cargoes and cargo receptors can influence COPII-mediated trafficking in equally profound ways. Together, these factors work in concert to ensure proper cargo movement in this first step of the secretory pathway. This article is part of a Special Issue entitled: Functional and structural diversity of endoplasmic reticulum.

Indexed as

AnimalsCOP-Coated VesiclesEndoplasmic ReticulumGolgi ApparatusHumansProtein TransportVesicular Transport ProteinsVesicular Transport Proteinsbstbypass-of-sec-thirteenCargo exportCargo receptorCLSDcoat protein II complexCOPIIcranio–lentinculo–sutural dysplasiacTAGE5cutaneous T-cell lymphoma-associated antigen 5endoplasmic reticulumEndoplasmic reticulumERERESER exit sitesERKextracellular signal-regulated kinaseGAPGEFglutathione S-transferaseglycosylphophatidylinositol-anchored proteinGPI-APGSTGTPase activating proteinguanine nucleotide exchange factorMAPKmitogen activated protein kinasePHphosphatidylinositol 4-phosphatepleckstrin homologyPtdIns4PTANGO1TFG-1transport and Golgi organization 1TRK-fused gene 1Vesiclevesicular stomatitis virus G proteinVSVG

Identifiers

PMID23419775
PMCPMC3676692
OpenAlexW2047261885

What OpenQuestion holds

Textmetadata
LicenceTDM
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.