Evidence map›Paper›PMID 17664431›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2007

Assays of vacuole fusion resolve the stages of docking, lipid mixing, and content mixing.

Youngsoo Jun, William Wickner

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

40 citing papers in PubMed, 84 citations in OpenAlex.

  1. Article
  2. SNARE Proteins in Synaptic Vesicle Fusion.Advances in neurobiology · 2023
    Article
  3. Review
  4. Article
  5. Article
  6. The NaMolecular biology of the cell · 2018
    Article
  7. Article
  8. Article
  9. Review
  10. Hemifusion in Synaptic Vesicle Cycle.Frontiers in molecular neuroscience · 2017
    Review
  11. Article
  12. Bioengineered yeast-derived vacuoles with enhanced tissue-penetrating ability for targeted cancer therapy.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  13. Article
  14. Article
  15. Vibrio effector protein VopQ inhibits fusion of V-ATPase-containing membranes.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  16. Towards reconstitution of membrane fusion mediated by SNAREs and other synaptic proteins.Critical reviews in biochemistry and molecular biology · 2015
    Review
  17. Article
  18. In vitro assay using engineered yeast vacuoles for neuronal SNARE-mediated membrane fusion.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  19. Plant vacuole morphology and vacuolar trafficking.Frontiers in plant science · 2014
    Review
  20. Studying protein-reconstituted proteoliposome fusion with content indicators in vitro.BioEssays : news and reviews in molecular, cellular and developmental biology · 2013
    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

2 authors at 1 institution in 1 country.

Youngsoo JunDepartment of Biochemistry, Dartmouth Medical School, Hanover, NH 03755-3844, USA.
William Wickner
Dartmouth College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Membrane fusion entails organelle docking and subsequent mixing of membrane bilayers and luminal compartments. We now present an in vitro assay of fusion, using yeast vacuoles bearing domains of either Fos or Jun fused to complementary halves of beta-lactamase. Upon fusion, these proteins associate to yield beta-lactamase activity. This assay complements the standard fusion assay (activation of pro-Pho8p in protease-deficient vacuoles by proteases from pho8Delta vacuoles). Both the beta-lactamase and pro-Pho8p activation assays of fusion show the same long kinetic delay between SNARE pairing and luminal compartment mixing. Lipid-mixing occurs rapidly after SNARE pairing but well before aqueous compartment mixing. These results support a model in which SNARE pairing leads to rapid hemifusion, followed by slow further lipid rearrangement and aqueous compartment mixing.

Indexed as

Membrane FusionAdenosine TriphosphateAlkaline Phosphatasebeta-LactamasesLipidsSNARE ProteinsVacuolesYeastsadenosine 5'-O-(3-thiotriphosphate)Adenosine TriphosphateAlkaline Phosphatasebeta-LactamasesLipidsSNARE Proteins

Identifiers

PMID17664431
PMCPMC1941832
OpenAlexW1978698410

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.