Evidence map›Paper›PMID 30190552›Full record

ArticleNature protocols2018

Preparation of asymmetric phospholipid vesicles for use as cell membrane models.

Milka Doktorova, Frederick A Heberle, Barbara Eicher, Robert F Standaert, John Katsaras, Erwin London, Georg Pabst, Drew Marquardt

Open access · greenAbstract read
In one paragraph

Article in Nature protocols, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
7.1field-weighted citation impact, top 2% 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

80 citing papers in PubMed, 166 citations in OpenAlex.

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20 more citing papers are in PubMed but not listed here.

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

8 authors at 6 institutions in 3 countries.

Milka Doktorova *Tri-Institutional PhD Program in Computational Biology and Medicine, Weill Cornell Medical College, New York, NY, USA.ORCID http://orcid.org/0000-0003-4366-2242
Frederick A Heberle *Large Scale Structures Group, Oak Ridge National Laboratory, Oak Ridge, TN, USA.
Barbara EicherInstitute of Molecular Biosciences, University of Graz, Graz, Austria.
Robert F StandaertLarge Scale Structures Group, Oak Ridge National Laboratory, Oak Ridge, TN, USA.
John KatsarasLarge Scale Structures Group, Oak Ridge National Laboratory, Oak Ridge, TN, USA.ORCID http://orcid.org/0000-0002-0424-3240
Erwin LondonDepartment of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, NY, USA.ORCID http://orcid.org/0000-0002-1295-0113
Georg PabstInstitute of Molecular Biosciences, University of Graz, Graz, Austria.
Drew MarquardtDepartment of Chemistry and Biochemistry, University of Windsor, Windsor, ON, Canada. drew.marquardt@uwindsor.ca.
Oak Ridge National Laboratory · USUniversity of Graz · ATCornell University · USEast Tennessee State University · USStony Brook University · USUniversity of Windsor · CA

Funding

Austrian Science Fund FWF P 27083
6 · The paper itself

Abstract

Freely suspended liposomes are widely used as model membranes for studying lipid-lipid and protein-lipid interactions. Liposomes prepared by conventional methods have chemically identical bilayer leaflets. By contrast, living cells actively maintain different lipid compositions in the two leaflets of the plasma membrane, resulting in asymmetric membrane properties that are critical for normal cell function. Here, we present a protocol for the preparation of unilamellar asymmetric phospholipid vesicles that better mimic biological membranes. Asymmetry is generated by methyl-β-cyclodextrin-catalyzed exchange of the outer leaflet lipids between vesicle pools of differing lipid composition. Lipid destined for the outer leaflet of the asymmetric vesicles is provided by heavy-donor multilamellar vesicles containing a dense sucrose core. Donor lipid is exchanged into extruded unilamellar acceptor vesicles that lack the sucrose core, facilitating the post-exchange separation of the donor and acceptor pools by centrifugation because of differences in vesicle size and density. We present two complementary assays allowing quantification of each leaflet's lipid composition: the overall lipid composition is determined by gas chromatography-mass spectrometry, whereas the lipid distribution between the two leaflets is determined by NMR, using the lanthanide shift reagent Pr

Indexed as

Cell MembraneGas Chromatography-Mass SpectrometryMagnetic Resonance SpectroscopyModels, BiologicalPhospholipidsUnilamellar LiposomesPhospholipidsUnilamellar Liposomes

Identifiers

PMID30190552
PMCPMC6459367
OpenAlexW2891006829

What OpenQuestion holds

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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 OpenQuestion graph.