Evidence map›Paper›PMID 34681757›Full record

ArticleInternational journal of molecular sciences2021

The Effect of the Osmotically Active Compound Concentration Difference on the Passive Water and Proton Fluxes across a Lipid Bilayer.

Magdalena Przybyło, Dominik Drabik, Joanna Doskocz, Aleš Iglič, Marek Langner

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Biophysical Considerations in Cell Fusion.Advances in experimental medicine and biology · 2026
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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.

Magdalena PrzybyłoDepartment of Biomedical Engineering, Wroclaw University of Science and Technology, Grunwaldzki 13, 50-377 Wrocław, Poland.
Dominik DrabikDepartment of Biomedical Engineering, Wroclaw University of Science and Technology, Grunwaldzki 13, 50-377 Wrocław, Poland.ORCID 0000-0003-4568-4066
Joanna DoskoczDepartment of Biomedical Engineering, Wroclaw University of Science and Technology, Grunwaldzki 13, 50-377 Wrocław, Poland.ORCID 0000-0002-7100-6237
Aleš IgličLaboratory of Physics, Faculty of Electrical Engineering, University of Ljubljana, Tržaška 25, SI-1000 Ljubljana, Slovenia.ORCID 0000-0002-7895-343X
Marek LangnerDepartment of Biomedical Engineering, Wroclaw University of Science and Technology, Grunwaldzki 13, 50-377 Wrocław, Poland.ORCID 0000-0003-1772-4550

Funding

National Centre for Research and Development POIR.04.01.04-00-0050/15Slovenian Research Agency P2-0232
6 · The paper itself

Abstract

The molecular details of the passive water flux across the hydrophobic membrane interior are still a matter of debate. One of the postulated mechanisms is the spontaneous, water-filled pore opening, which facilitates the hydrophilic connection between aqueous phases separated by the membrane. In the paper, we provide experimental evidence showing that the spontaneous lipid pore formation correlates with the membrane mechanics; hence, it depends on the composition of the lipid bilayer and the concentration of the osmotically active compound. Using liposomes as an experimental membrane model, osmotically induced water efflux was measured with the stopped-flow technique. Shapes of kinetic curves obtained at low osmotic pressure differences are interpreted in terms of two events: the lipid pore opening and water flow across the aqueous channel. The biological significance of the dependence of the lipid pore formation on the concentration difference of an osmotically active compound was illustrated by the demonstration that osmotically driven water flow can be accompanied by the dissipation of the pH gradient. The application of the Helfrich model to describe the probability of lipid pore opening was validated by demonstrating that the probability of pore opening correlates with the membrane bending rigidity. The correlation was determined by experimentally derived bending rigidity coefficients and probabilities of lipid pores opening.

Indexed as

Cell MembraneEggsHydrogen-Ion ConcentrationKineticsLightLipid BilayersLiposomesLysophosphatidylcholinesMembrane LipidsModels, ChemicalOsmotic PressurePhosphatidylcholinesPhosphatidylethanolaminesProtonsWaterLipid BilayersLiposomesLysophosphatidylcholinesMembrane LipidsPhosphatidylcholinesphosphatidylethanolaminePhosphatidylethanolaminesProtonsWaterlipid bilayermembrane mechanicsproton transportwater activitywater transport

Identifiers

PMID34681757
PMCPMC8540289

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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.