Evidence map›Paper›PMID 37120716›Full record

ArticleBiophysical journal2023

Distributing aminophospholipids asymmetrically across leaflets causes anomalous membrane stiffening.

Moritz P K Frewein, Paulina Piller, Enrico F Semeraro, Orsolya Czakkel, Yuri Gerelli, Lionel Porcar, Georg Pabst

Open access · hybridAbstract read
In one paragraph

Article in Biophysical journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.1field-weighted citation impact, top 8% of its field
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

7 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Article
  3. Loss of lipid asymmetry facilitates plasma membrane blebbing by decreasing membrane lipid packing.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
  5. Article
  6. Article
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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

7 authors at 3 institutions in 3 countries.

Moritz P K FreweinBiophysics, Institute of Molecular Biosciences, University of Graz, NAWI Graz, Graz, Austria; Institut Laue-Langevin, Grenoble, France; BioTechMed Graz, Graz, Austria; Field of Excellence BioHealth, Graz, Austria.
Paulina PillerBiophysics, Institute of Molecular Biosciences, University of Graz, NAWI Graz, Graz, Austria; BioTechMed Graz, Graz, Austria; Field of Excellence BioHealth, Graz, Austria.
Enrico F SemeraroBiophysics, Institute of Molecular Biosciences, University of Graz, NAWI Graz, Graz, Austria; BioTechMed Graz, Graz, Austria; Field of Excellence BioHealth, Graz, Austria.
Orsolya CzakkelInstitut Laue-Langevin, Grenoble, France.
Yuri GerelliCNR Institute for Complex Systems, Uos Sapienza, Roma, Italy; Department of Physics, Sapienza University of Rome, Roma, Italy.
Lionel PorcarInstitut Laue-Langevin, Grenoble, France.
Georg PabstBiophysics, Institute of Molecular Biosciences, University of Graz, NAWI Graz, Graz, Austria; BioTechMed Graz, Graz, Austria; Field of Excellence BioHealth, Graz, Austria. Electronic address: georg.pabst@uni-graz.at.
University of Graz · ATInstitut Laue-Langevin · FRInstitute for Complex Systems · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We studied the mechanical leaflet coupling of prototypic mammalian plasma membranes using neutron spin-echo spectroscopy. In particular, we examined a series of asymmetric phospholipid vesicles with phosphatidylcholine and sphingomyelin enriched in the outer leaflet and inner leaflets composed of phosphatidylethanolamine/phosphatidylserine mixtures. The bending rigidities of most asymmetric membranes were anomalously high, exceeding even those of symmetric membranes formed from their cognate leaflets. Only asymmetric vesicles with outer leaflets enriched in sphingolipid displayed bending rigidities in conformity with these symmetric controls. We performed complementary small-angle neutron and x-ray experiments on the same vesicles to examine possible links to structural coupling mechanisms, which would show up in corresponding changes in membrane thickness. In addition, we estimated differential stress between leaflets originating either from a mismatch of their lateral areas or spontaneous curvatures. However, no correlation with asymmetry-induced membrane stiffening was observed. To reconcile our findings, we speculate that an asymmetric distribution of charged or H-bond forming lipids may induce an intraleaflet coupling, which increases the weight of hard undulatory modes of membrane fluctuations and hence the overall membrane stiffness.

Indexed as

PhosphatidylcholinesPhospholipidsAnimalsCell MembraneLipid BilayersMammalsMembranesSphingomyelinsLipid BilayersPhosphatidylcholinesPhospholipidsSphingomyelins

Identifiers

PMID37120716
PMCPMC10322881
OpenAlexW4367301392

What Socratic holds

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LicenceCC BY
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 Socratic graph.