Evidence map›Paper›PMID 38822521›Full record

ArticleBiophysical journal2024

Effect of leaflet asymmetry on the stretching elasticity of lipid bilayers with phosphatidic acid.

Dominik Drabik, Piotr Hinc, Mareike Stephan, Rafaela R M Cavalcanti, Aleksander Czogalla, Rumiana Dimova

Abstract read
In one paragraph

Article in Biophysical journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 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

6 authors.

Dominik DrabikDepartment of Cytobiochemistry, Faculty of Biotechnology, University of Wroclaw, Wroclaw, Poland; Max Planck Institute of Colloids and Interfaces, Potsdam, Germany; Department of Biomedical Engineering, Wroclaw University of Science and Technology, Wroclaw, Poland. Electronic address: dominik.drabik@pwr.edu.pl.
Piotr HincDepartment of Cytobiochemistry, Faculty of Biotechnology, University of Wroclaw, Wroclaw, Poland.
Mareike StephanMax Planck Institute of Colloids and Interfaces, Potsdam, Germany.
Rafaela R M CavalcantiMax Planck Institute of Colloids and Interfaces, Potsdam, Germany.
Aleksander CzogallaDepartment of Cytobiochemistry, Faculty of Biotechnology, University of Wroclaw, Wroclaw, Poland. Electronic address: aleksander.czogalla@uwr.edu.pl.
Rumiana DimovaMax Planck Institute of Colloids and Interfaces, Potsdam, Germany. Electronic address: rumiana.dimova@mpikg.mpg.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The asymmetry of membranes has a significant impact on their biophysical characteristics and behavior. This study investigates the composition and mechanical properties of symmetric and asymmetric membranes in giant unilamellar vesicles (GUVs) made of palmitoyloleoyl phosphatidylcholine (POPC) and palmitoyloleoyl phosphatidic acid (POPA). A combination of fluorescence quantification, zeta potential measurements, micropipette aspiration, and bilayer molecular dynamics simulations are used to characterize these membranes. The outer leaflet composition in vesicles is found consistent across the two preparation methods we employed, namely electroformation and inverted emulsion transfer. However, characterizing the inner leaflet poses challenges. Micropipette aspiration of GUVs show that oil residues do not substantially alter membrane elasticity, but simulations reveal increased membrane thickness and decreased interleaflet coupling in the presence of oil. Asymmetric membranes with a POPC:POPA mixture in the outer leaflet and POPC in the inner leaflet display similar stretching elasticity values to symmetric POPC:POPA membranes, suggesting potential POPA insertion into the inner leaflet during vesicle formation and suppressed asymmetry. The inverse compositional asymmetry, with POPC in the outer leaflet and POPC:POPA in the inner one yield less stretchable membranes with higher compressibility modulus compared with their symmetric counterparts. Challenges in achieving and predicting compositional correspondence highlight the limitations of phase-transfer-based methods. In addition, caution is advised when using fluorescently labeled lipids (even at low fractions of 0.5 mol %), as unexpected gel-like domains in symmetric POPC:POPA membranes were observed only with a specific type of labeled DOPE (dioleoylphosphatidylethanolamine) and the same fraction of unlabeled DOPE. The latter suggest that such domain formation may result from interactions between lipids and membrane fluorescent probes. Overall, this study underscores the complexity of factors influencing GUV membrane asymmetry, emphasizing the need for further research and improvement of characterization techniques.

Indexed as

ElasticityLipid BilayersPhosphatidic AcidsUnilamellar LiposomesMolecular Dynamics SimulationPhosphatidylcholines1-palmitoyl-2-oleoylphosphatidylcholineLipid BilayersPhosphatidic AcidsPhosphatidylcholinesUnilamellar Liposomes

Identifiers

PMID38822521
PMCPMC11365108

What Socratic holds

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LicenceCC BY
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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 Socratic graph.