Evidence map›Paper›PMID 23536066›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2013

Dance of the SNAREs: assembly and rearrangements detected with FRET at neuronal synapses.

Vadim Degtyar, Ismail M Hafez, Christopher Bray, Robert S Zucker

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
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

18 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Structural characterization of the Rabphilin-3A-SNAP25 interaction.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  7. Article
  8. Millisecond CaProceedings of the Japan Academy. Series B, Physical and biological sciences · 2017
    Review
  9. Article
  10. Article
  11. Article
  12. Munc18c: a controversial regulator of peripheral insulin action.Trends in endocrinology and metabolism: TEM · 2014
    Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Exocytosis through the Lens.Frontiers in endocrinology · 2013
    Review
  18. 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

4 authors.

Vadim DegtyarDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, California 94720, USA.
Ismail M Hafez
Christopher Bray
Robert S Zucker

Funding

SNARE Protein Dynamics during Synaptic TransmissionR01NS054760 · NINDS · UNIVERSITY OF CALIFORNIA BERKELEY · PI ZUCKER, ROBERT STEPHEN · 2007 to 2011
$1.6M
Changes/SNARE Proteins/Neural Transmission/FRETR21NS048016 · NINDS · UNIVERSITY OF CALIFORNIA BERKELEY · PI ZUCKER, ROBERT STEPHEN · 2004 to 2005
$352k
NINDS NIH HHS R01 NS054760NINDS NIH HHS R21 NS048016
6 · The paper itself

Abstract

Soluble N-ethylmaleimide-sensitive fusion protein attachment protein receptors (SNAREs) mediate vesicle fusion with the plasma membrane on activation by calcium binding to synaptotagmin. In the present study, we used fluorescence resonance energy transfer (FRET) and fluorescence lifetime imaging microscopy between fluorescently labeled SNARE proteins expressed in cultured rat hippocampal neurons to detect resting SNARE complexes, their conformational rearrangement on exocytosis, their disassembly before endocytosis of vesicular proteins, and SNARE assembly at newly docked vesicles. Assembled SNAREs are not only present in docked vesicles; unexpected residual "orphan SNARE complexes" also reside in para-active zone regions. Real-time changes in FRET between N-terminally labeled SNAP-25 and VAMP reported a reorientation of the SNARE motif upon exocytosis, SNARE disassembly in the active zone periphery, and SNARE reassembly in newly docked vesicles. With VAMP labeled C-terminally, decreased fluorescence in C-terminally labeled syntaxin (extracellular) reported trans-cis-conformational changes in SNAREs on vesicle fusion. After fusion SNAP-25 and syntaxin disperse along with VAMP, as well as the FRET signal itself, indicating diffusion of intact SNAREs after vesicle fusion but before their peripheral disassembly. Our measurements of spatiotemporal dynamics of SNARE conformational changes and movements refine models of SNARE function. Technical advances required to detect tiny changes in fluorescence in small fractions of labeled proteins in presynaptic boutons on a time scale of seconds permit the detection of rapid intermolecular interactions between small proportions of protein partners in cellular subcompartments.

Indexed as

AnimalsCell MembraneCells, CulturedCeruleninElectric StimulationEmbryo, MammalianExocytosisFemaleFluorescence Resonance Energy TransferGreen Fluorescent ProteinsHippocampusImage Processing, Computer-AssistedMaleModels, BiologicalMutationNeuronsCeruleninFM 4-64Green Fluorescent ProteinsPyridinium CompoundsQuaternary Ammonium CompoundsSnap25 protein, ratSNARE ProteinsSynaptosomal-Associated Protein 25Syntaxin 1Vamp2 protein, ratVesicle-Associated Membrane Protein 2

Identifiers

PMID23536066
PMCPMC3647469

What OpenQuestion holds

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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.