Evidence map›Paper›PMID 16214871›Full record

ArticleBiophysical journal2006

Lipid asymmetry in DLPC/DSPC-supported lipid bilayers: a combined AFM and fluorescence microscopy study.

Wan-Chen Lin, Craig D Blanchette, Timothy V Ratto, Marjorie L Longo

Abstract read
In one paragraph

Article in Biophysical journal, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing 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

44 citing papers in PubMed.

  1. Review
  2. Article
  3. Domain Localization by Graphene Oxide in Supported Lipid Bilayers.International journal of molecular sciences · 2023
    Article
  4. Single-Molecule Trapping and Measurement in a Nanostructured Lipid Bilayer System.Langmuir : the ACS journal of surfaces and colloids · 2022
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Polar Lipid Fraction E fromInternational journal of molecular sciences · 2020
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Interleaflet Coupling of Lipid Nanodomains - Insights FromFrontiers in cell and developmental biology · 2020
    Review
  15. Do ABC transporters regulate plasma membrane organization?Cellular & molecular biology letters · 2020
    Review
  16. Article
  17. Article
  18. Asymmetric Hybrid Polymer-Lipid Giant Vesicles as Cell Membrane Mimics.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2018
    Article
  19. Article
  20. 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

4 authors.

Wan-Chen LinBiophysics Graduate Group, Division of Biological Sciences, University of California, Davis, California 95616, USA.
Craig D Blanchette
Timothy V Ratto
Marjorie L Longo

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A fundamental attribute of cell membranes is transmembrane asymmetry, specifically the formation of ordered phase domains in one leaflet that are compositionally different from the opposing leaflet of the bilayer. Using model membrane systems, many previous studies have demonstrated the formation of ordered phase domains that display complete transmembrane symmetry; but there have been few reports on the more biologically relevant asymmetric membrane structures. Here we report on a combined atomic force microscopy and fluorescence microscopy study whereby we observe three different states of transmembrane symmetry in phase-separated supported lipid bilayers formed by vesicle fusion. We find that if the leaflets differ in gel-phase area fraction, then the smaller domains in one leaflet are in registry with the larger domains in the other leaflet and the system is dynamic. In a presumed lipid flip-flop process similar to Ostwald ripening, the smaller domains in one leaflet erode away whereas the large domains in the other leaflet grow until complete compositional asymmetry is reached and remains stable. We have quantified this evolution and determined that the lipid flip-flop event happens most frequently at the interface between symmetric and asymmetric DSPC domains. If both leaflets have identical area fraction of gel-phase, gel-phase domains are in registry and are static in comparison to the first state. The stability of these three DSPC domain distributions, the degree of registry observed, and the domain immobility have biological significance with regards to maintenance of lipid asymmetry in living cell membranes, communication between inner leaflet and outer leaflet, membrane adhesion, and raft mobility.

Indexed as

4-Chloro-7-nitrobenzofurazanBiophysicsCell AdhesionCell MembraneLipid BilayersLipidsMembrane FluidityMembrane MicrodomainsMicroscopy, Atomic ForceMicroscopy, FluorescenceModels, StatisticalNormal DistributionPhosphatidylcholinesProtein Structure, TertiaryTemperatureTime Factors1,2-distearoyllecithin1,2-linoleoylphosphatidylcholine1-acyl-2-(12-((7-nitrobenz-2-oxa-1,3-diazol-4-yl)amino)dodecanoyl)phosphatidylcholine4-Chloro-7-nitrobenzofurazanLipid BilayersLipidsPhosphatidylcholines

Identifiers

PMID16214871
PMCPMC1367021

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.