Evidence map›Paper›PMID 27074681›Full record

ArticleBiophysical journal2016

Lipid Interactions and Organization in Complex Bilayer Membranes.

Oskar Engberg, Tomokazu Yasuda, Victor Hautala, Nobuaki Matsumori, Thomas K M Nyholm, Michio Murata, J Peter Slotte

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

12 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Sea Anemones, Actinoporins, and Cholesterol.International journal of molecular sciences · 2022
    Review
  3. Article
  4. Article
  5. Article
  6. On the existence of endocytosis driven by membrane phase separations.Biochimica et biophysica acta. Biomembranes · 2020
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
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 2 countries.

Oskar EngbergBiochemistry, Faculty of Science and Engineering, Åbo Akademi University, Turku, Finland.
Tomokazu YasudaDepartment of Chemistry, Graduate School of Science, Osaka University, Toyonaka, Osaka, Japan; Lipid Active Structure Project, Japan Science and Technology Agency, ERATO, Toyonaka, Osaka, Japan.
Victor HautalaBiochemistry, Faculty of Science and Engineering, Åbo Akademi University, Turku, Finland.
Nobuaki MatsumoriDepartment of Chemistry, Graduate School of Science, Osaka University, Toyonaka, Osaka, Japan; Department of Chemistry, Faculty of Science, Kyushu University, Fukuoka, Japan.
Thomas K M NyholmBiochemistry, Faculty of Science and Engineering, Åbo Akademi University, Turku, Finland.
Michio MurataDepartment of Chemistry, Graduate School of Science, Osaka University, Toyonaka, Osaka, Japan; Lipid Active Structure Project, Japan Science and Technology Agency, ERATO, Toyonaka, Osaka, Japan. Electronic address: murata@chem.sci.osaka-u.ac.jp.
J Peter SlotteBiochemistry, Faculty of Science and Engineering, Åbo Akademi University, Turku, Finland. Electronic address: jpslotte@abo.fi.
Åbo Akademi University · FIOsaka University · JPJapan Science and Technology Agency · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bilayer lipids influence the lateral structure of the membranes, but the relationship between lipid properties and the lateral structure formed is not always understood. Model membrane studies on bilayers containing cholesterol and various phospholipids (PLs) suggest that high and low temperature melting PLs may segregate, especially in the presence of cholesterol. The effect of different PL headgroups on lateral structure of bilayers is also not clear. Here, we have examined the formation of lateral heterogeneity in increasingly complex (up to five-component) multilamellar bilayers. We have used time-resolved fluorescence spectroscopy with domain-selective fluorescent probes (PL-conjugated trans-parinaric acid), and (2)H NMR spectroscopy with site or perdeuterated PLs. We have measured changes in bilayer order using such domain-selective probes both as a function of temperature and composition. Our results from time-resolved fluorescence and (2)H NMR showed that in ternary bilayers, acyl chain order and thermostability in sphingomyelin-rich domains were not affected to any greater extent by the headgroup structure of the monounsaturated PLs (phosphatidylcholine, phosphatidylethanolamine, or phosphatidylserine) in the bilayer. In the complex five-component bilayers, we could not detect major differences between the different monounsaturated PLs regarding cholesterol-induced ordering. However, cholesterol clearly influenced deuterated N-palmitoyl sphingomyelin differently than the other deuterated PLs, suggesting that cholesterol favored N-palmitoyl sphingomyelin over the other PLs. Taken together, both the fluorescence spectroscopy and (2)H NMR data suggest that the complex five-component membranes displayed lateral heterogeneity, at least in the lower temperature regimen examined.

Indexed as

Cell MembraneLipid BilayersPhospholipidsLipid BilayersPhospholipids

Identifiers

PMID27074681
PMCPMC4833832
OpenAlexW2340451352

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.