Evidence map›Paper›PMID 17872963›Full record

ArticleBiophysical journal2008

Atomic force microscope spectroscopy reveals a hemifusion intermediate during soluble N-ethylmaleimide-sensitive factor-attachment protein receptors-mediated membrane fusion.

Midhat H Abdulreda, Akhil Bhalla, Edwin R Chapman, Vincent T Moy

Abstract read
In one paragraph

Article in Biophysical journal, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Pulling force generated by interacting SNAREs facilitates membrane hemifusion.Integrative biology : quantitative biosciences from nano to macro · 2009
    Article
  9. Article
  10. Article
  11. The fusion pores of Ca2+ -triggered exocytosis.Nature structural & molecular biology · 2008
    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.

Midhat H AbdulredaUniversity of Miami Miller School of Medicine, Physiology and Biophysics Department, Miami, Florida 33136, USA.
Akhil Bhalla
Edwin R Chapman
Vincent T Moy

Funding

Synaptotagmin C2B Domain as a Ca2+ Sensing ModuleR01MH061876 · NIMH · UNIVERSITY OF WISCONSIN-MADISON · PI Edwin R Chapman · 2002 to 2026
$7.7M
SYNAPTOTAGMIN IN EXCITATION/SECRETION COUPLINGR01GM056827 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI CHAPMAN, EDWIN R · 1998 to 2006
$1.8M
Protein-mediated molecular adhesion: AFM studiesR01GM055611 · NIGMS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI MOY, VINCENT T · 2003 to 2006
$932k
PROTEIN MEDIATED MOLECULAR ADHESION--AFM STUDIESR29GM055611 · NIGMS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI MOY, VINCENT T · 1997 to 2001
$315k
NIGMS NIH HHS GM55611NIGMS NIH HHS GM56827NIGMS NIH HHS R01 GM055611NIGMS NIH HHS R01 GM056827NIGMS NIH HHS R29 GM055611NIMH NIH HHS MH61876NIMH NIH HHS R01 MH061876
6 · The paper itself

Abstract

This study investigated the effect of soluble N-ethylmaleimide-sensitive factor-attachment protein (SNAP) receptors (SNAREs) on the fusion of egg L-alpha-phosphatidylcholine bilayers using atomic force microscope (AFM) spectroscopy. AFM measurements of the fusion force under compression were acquired to reveal the energy landscape of the fusion process. A single main energy barrier governing the fusion process was identified in the absence and presence of SNAREs in the bilayers. Under compression, a significant downward shift in the fusion dynamic force spectrum was observed when cognate v- and t-SNAREs were present in the opposite bilayers. The presence of vesicle-associated membrane protein (VAMP) and binary syntaxin and SNAP 25 in the apposed bilayers resulted in a reduction in the height of the activation potential by approximately 1.3 k(B)T and a >2-fold increase in the width of the energy barrier. The widening of the energy barrier in the presence SNAREs is interpreted as an increase in the compressibility of the membranes, which translates to a greater ease in the bilayer deformation and subsequently the fusion of the membranes under compression. Facilitation of membrane fusion was observed only when SNAREs were present in both bilayers. Moreover, addition of the soluble cytoplasmic domain of VAMP, which interferes with the interaction between opposing v- and t-SNAREs, prevented such facilitation. These observations implicated the interaction between the cytoplasmic domains of opposing SNAREs in the observed fusion facilitation, possibly by destabilizing the bilayers through pulling on their transmembrane segments. Our AFM compression measurements revealed that SNARE-mediated membrane fusion proceeded through a sequence of two approximately 5 nm collapses of the membrane, an observation that is consistent with the existence of a hemifused state during the fusion process.

Indexed as

Membrane FusionMicroscopy, Atomic ForceAnimalsSNARE ProteinsSolubilityThermodynamicsSNARE Proteins

Identifiers

PMID17872963
PMCPMC2157233

What OpenQuestion holds

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Registered trials

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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.