Evidence map›Paper›PMID 26153707›Full record

ArticleBiophysical journal2015

Tuning membrane thickness fluctuations in model lipid bilayers.

Rana Ashkar, Michihiro Nagao, Paul D Butler, Andrea C Woodka, Mani K Sen, Tadanori Koga

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

21 citing papers in PubMed, 58 citations in OpenAlex.

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  11. Scaling relationships for the elastic moduli and viscosity of mixed lipid membranes.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  12. How cholesterol stiffens unsaturated lipid membranes.Proceedings of the National Academy of Sciences of the United States of America · 2020
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  13. Article
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  15. Interleaflet coupling of n-alkane incorporated bilayers.Physical chemistry chemical physics : PCCP · 2020
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  18. Time-resolved measurements of an ion channel conformational change driven by a membrane phase transition.Proceedings of the National Academy of Sciences of the United States of America · 2017
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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

6 authors at 3 institutions in 1 country.

Rana AshkarNational Institute of Standards and Technology (NIST) Center for Neutron Research, National Institute of Standards and Technology, Gaithersburg, Maryland; Department of Material Science and Engineering, University of Maryland, College Park, Maryland.
Michihiro NagaoNational Institute of Standards and Technology (NIST) Center for Neutron Research, National Institute of Standards and Technology, Gaithersburg, Maryland; Center for Exploration of Energy and Matter, Indiana University, Bloomington, Indiana. Electronic address: mnagao@indiana.edu.
Paul D ButlerNational Institute of Standards and Technology (NIST) Center for Neutron Research, National Institute of Standards and Technology, Gaithersburg, Maryland; Department of Chemical & Biomolecular Engineering, University of Delaware, Newark, Delaware.
Andrea C WoodkaDepartment of Chemistry & Life Science, United States Military Academy, West Point, New York.
Mani K SenDepartment of Materials Science and Engineering, Stony Brook University, Stony Brook, New York.
Tadanori KogaDepartment of Materials Science and Engineering, Stony Brook University, Stony Brook, New York; Chemical and Molecular Engineering Program, Stony Brook University, Stony Brook, New York.
National Institute of Standards and Technology · USStony Brook University · USUnited States Military Academy · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Membrane thickness fluctuations have been associated with a variety of critical membrane phenomena, such as cellular exchange, pore formation, and protein binding, which are intimately related to cell functionality and effective pharmaceuticals. Therefore, understanding how these fluctuations are controlled can remarkably impact medical applications involving selective macromolecule binding and efficient cellular drug intake. Interestingly, previous reports on single-component bilayers show almost identical thickness fluctuation patterns for all investigated lipid tail-lengths, with similar temperature-independent membrane thickness fluctuation amplitude in the fluid phase and a rapid suppression of fluctuations upon transition to the gel phase. Presumably, in vivo functions require a tunability of these parameters, suggesting that more complex model systems are necessary. In this study, we explore lipid tail-length mismatch as a regulator for membrane fluctuations. Unilamellar vesicles of an equimolar mixture of dimyristoylphosphatidylcholine and distearoylphosphatidylcholine molecules, with different tail-lengths and melting transition temperatures, are used as a model system for this next level of complexity. Indeed, this binary system exhibits a significant response of membrane dynamics to thermal variations. The system also suggests a decoupling of the amplitude and the relaxation time of the membrane thickness fluctuations, implying a potential for independent control of these two key parameters.

Indexed as

Models, ChemicalDimyristoylphosphatidylcholineLipid BilayersNeutron DiffractionPhosphatidylcholinesScattering, Small AngleSpectrum AnalysisTransition TemperatureUnilamellar LiposomesX-Ray Diffraction1,2-distearoyllecithinDimyristoylphosphatidylcholineLipid BilayersPhosphatidylcholinesUnilamellar Liposomes

Identifiers

PMID26153707
PMCPMC4571027
OpenAlexW2111638891

What OpenQuestion holds

Textmetadata
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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.