Evidence map›Paper›PMID 30665697›Full record

ArticleBiophysical journal2019

Complex Phase Behavior of GUVs Containing Different Sphingomyelins.

Daniel Balleza, Andrea Mescola, Nathaly Marín-Medina, Gregorio Ragazzini, Marco Pieruccini, Paolo Facci, Andrea Alessandrini

Abstract read
In one paragraph

Article in Biophysical journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Spectroscopic Analysis of the Binding of Paraquat and Diquat Herbicides to Biosubstrates.International journal of environmental research and public health · 2021
    Article
  11. Viennamycins: Lipopeptides Produced by aJournal of natural products · 2020
    Article
  12. Article
  13. Synthesis of GbAngewandte Chemie (International ed. in English) · 2019
    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.

Daniel BallezaIstituto Nanoscienze CNR, S3, Modena, Italy.
Andrea MescolaIstituto Nanoscienze CNR, S3, Modena, Italy.
Nathaly Marín-MedinaDepartamento de Física, Universidad de Los Andes, Bogotá, Colombia.
Gregorio RagazziniIstituto Nanoscienze CNR, S3, Modena, Italy; Dipartimento di Scienze Fisiche, Matematiche e Informatiche, Università di Modena e Reggio Emilia, Modena, Italy.
Marco PierucciniIstituto Nanoscienze CNR, S3, Modena, Italy.
Paolo FacciCNR - Istituto di Biofisica, Genova, Italy.
Andrea AlessandriniIstituto Nanoscienze CNR, S3, Modena, Italy; Dipartimento di Scienze Fisiche, Matematiche e Informatiche, Università di Modena e Reggio Emilia, Modena, Italy. Electronic address: andrea.alessandrini@unimore.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Understanding the lateral organization of biological membranes plays a key role on the road to fully appreciate the physiological functions of this fundamental barrier between the inside and outside regions of a cell. Ternary lipid bilayers composed of a high and a low melting temperature lipid and cholesterol represent a model system that mimics some of the important thermodynamical features of much more complex lipid mixtures such as those found in mammal membranes. The phase diagram of these ternary mixtures can be studied exploiting fluorescence microscopy in giant unilamellar vesicles, and it is typically expected to give rise, for specific combinations of composition and temperature, to regions of two-phase coexistence and a region with three-phase coexistence, namely, the liquid-ordered, liquid-disordered, and solid phases. Whereas the observation of two-phase coexistence is routinely possible using fluorescence microscopy, the three-phase region is more elusive to study. In this article, we show that particular lipid mixtures containing diphytanoyl-phosphatidylcholine and cholesterol plus different types of sphingomyelin (SM) are prone to produce bilayer regions with more than two levels of fluorescence intensity. We found that these intensity levels occur at low temperature and are linked to the copresence of long and asymmetric chains in SMs and diphytanoyl-phosphatidylcholine in the lipid mixtures. We discuss the possible interpretations for this observation in terms of bilayer phase organization in the presence of sphingolipids. Additionally, we also show that in some cases, liposomes in the three-phase coexistence state exhibit extreme sensitivity to lateral tension. We hypothesize that the appearance of the different phases is related to the asymmetric structure of SMs and to interdigitation effects.

Indexed as

CholesterolSphingomyelinsStress, MechanicalTemperatureUnilamellar LiposomesCholesterolSphingomyelinsUnilamellar Liposomes

Identifiers

PMID30665697
PMCPMC6369432

What OpenQuestion holds

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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.