Evidence map›Paper›PMID 20371318›Full record

ArticleBiophysical journal2010

Direct visualization of large and protein-free hemifusion diaphragms.

Jörg Nikolaus, Martin Stöckl, Dieter Langosch, Rudolf Volkmer, Andreas Herrmann

Abstract read
In one paragraph

Article in Biophysical journal, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed.

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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.

Jörg NikolausInstitute of Biology, Faculty of Mathematics and Natural Sciences, Humboldt-University Berlin, Berlin, Germany.
Martin Stöckl
Dieter Langosch
Rudolf Volkmer
Andreas Herrmann

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fusion of cellular membranes is a ubiquitous biological process requiring remodeling of two phospholipid bilayers. We believe it is very likely that merging of membranes proceeds via similar sequential intermediates. Contacting membranes form a stalk between the proximal leaflets that expands radially into an hemifusion diaphragm (HD) and subsequently open to a fusion pore. Although considered to be a key intermediate in fusion, direct experimental verification of this structure is difficult due to its transient nature. Using confocal fluorescence microscopy we have investigated the fusion of giant unilamellar vesicles (GUVs) containing phosphatidylserine and fluorescent virus derived transmembrane peptides or membrane proteins in the presence of divalent cations. Time-resolved imaging revealed that fusion was preceded by displacement of peptides and fluorescent lipid analogs from the GUV-GUV adhesion region. A detailed analysis of this area being several mum in size revealed that peptides were completely sequestered as expected for an HD. Lateral distribution of lipid analogs was consistent with formation of an HD but not with the presence of two adherent bilayers. Formation and size of the HD were dependent on lipid composition and peptide concentration.

Indexed as

AnimalsBiophysicsCalciumCationsFluorescence Recovery After PhotobleachingFluorescent DyesLipid BilayersLipidsMicroscopy, ConfocalMicroscopy, FluorescencePeptidesPhosphatidylserinesPhospholipidsUnilamellar LiposomesVirusesCalciumCationsFluorescent DyesLipid BilayersLipidsPeptidesPhosphatidylserinesPhospholipidsUnilamellar Liposomes

Identifiers

PMID20371318
PMCPMC2849057

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.