Evidence map›Paper›PMID 27815573›Full record

ArticleEuropean biophysics journal : EBJ2017

Solubilization of lipids and lipid phases by the styrene-maleic acid copolymer.

Juan J Dominguez Pardo, Jonas M Dörr, Aditya Iyer, Ruud C Cox, Stefan Scheidelaar, Martijn C Koorengevel, Vinod Subramaniam, J Antoinette Killian

Abstract read
In one paragraph

Article in European biophysics journal : EBJ, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

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  8. Biological insights from SMA-extracted proteins.Biochemical Society transactions · 2021
    Review
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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

8 authors.

Juan J Dominguez PardoDepartment of Chemistry, Faculty of Science, Membrane Biochemistry and Biophysics, Bijvoet Center for Biomolecular Research, Padualaan 8, 3584, Utrecht, The Netherlands. J.J.DominguezPardo@uu.nl.ORCID http://orcid.org/0000-0002-8563-2466
Jonas M DörrDepartment of Chemistry, Faculty of Science, Membrane Biochemistry and Biophysics, Bijvoet Center for Biomolecular Research, Padualaan 8, 3584, Utrecht, The Netherlands.
Aditya IyerNanoscale Biophysics Group, FOM Institute AMOLF, Science Park 104, 1098, Amsterdam, The Netherlands.
Ruud C CoxDepartment of Chemistry, Faculty of Science, Membrane Biochemistry and Biophysics, Bijvoet Center for Biomolecular Research, Padualaan 8, 3584, Utrecht, The Netherlands.
Stefan ScheidelaarDepartment of Chemistry, Faculty of Science, Membrane Biochemistry and Biophysics, Bijvoet Center for Biomolecular Research, Padualaan 8, 3584, Utrecht, The Netherlands.
Martijn C KoorengevelDepartment of Chemistry, Faculty of Science, Membrane Biochemistry and Biophysics, Bijvoet Center for Biomolecular Research, Padualaan 8, 3584, Utrecht, The Netherlands.
Vinod SubramaniamNanoscale Biophysics Group, FOM Institute AMOLF, Science Park 104, 1098, Amsterdam, The Netherlands.
J Antoinette KillianDepartment of Chemistry, Faculty of Science, Membrane Biochemistry and Biophysics, Bijvoet Center for Biomolecular Research, Padualaan 8, 3584, Utrecht, The Netherlands. J.A.Killian@uu.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A promising tool in membrane research is the use of the styrene-maleic acid (SMA) copolymer to solubilize membranes in the form of nanodiscs. Since membranes are heterogeneous in composition, it is important to know whether SMA thereby has a preference for solubilization of either specific types of lipids or specific bilayer phases. Here, we investigated this by performing partial solubilization of model membranes and analyzing the lipid composition of the solubilized fraction. We found that SMA displays no significant lipid preference in homogeneous binary lipid mixtures in the fluid phase, even when using lipids that by themselves show very different solubilization kinetics. By contrast, in heterogeneous phase-separated bilayers, SMA was found to have a strong preference for solubilization of lipids in the fluid phase as compared to those in either a gel phase or a liquid-ordered phase. Together the results suggest that (1) SMA is a reliable tool to characterize native interactions between membrane constituents, (2) any solubilization preference of SMA is not due to properties of individual lipids but rather due to properties of the membrane or membrane domains in which these lipids reside and (3) exploiting SMA resistance rather than detergent resistance may be an attractive approach for the isolation of ordered domains from biological membranes.

Indexed as

Cell MembraneLipid BilayersMaleatesPolystyrenesSolubilityLipid BilayersMaleatesmaleic acidPolystyrenesstyrofoamLipid–protein interactionsLipid raftsNanodiscsSMALPSMA-resistant membrane (SRM)Styrene–maleic acid

Identifiers

PMID27815573
PMCPMC5209432

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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.