Evidence map›Paper›PMID 17496041›Full record

ArticleBiophysical journal2007

Lipid lateral segregation driven by diacyl cyclodextrin interactions at the membrane surface.

Michel Roux, Stéphane Moutard, Bruno Perly, Florence Djedaini-Pilard

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

2 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Self-assemblies of amphiphilic cyclodextrins.European biophysics journal : EBJ · 2007
    Review
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

4 authors at 4 institutions in 1 country.

Michel RouxCommissariat à l'Energie Atomique/Direction des Sciences du Vivant/Institut de Biologie et Technologies de Saclay, URA CNRS, Service de Bioénergétique, Biologie Structurale et Mécanismes, Gif sur Yvette Cedex, France. michel.roux@cea.fr
Stéphane Moutard
Bruno Perly
Florence Djedaini-Pilard
Centre National de la Recherche Scientifique · FRCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FROZ Biosciences (France) · FRUniversité de Picardie Jules Verne · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cyclodextrins are hydrophilic molecular cages with a hydrophobic interior allowing the inclusion of water-insoluble drugs. Amphiphilic cyclodextrins obtained by appending a hydrophobic anchor were designed to improve the cell targeting of the drug-containing cavities through their liposome transportation in the organism. After insertion in model membranes, they were found to induce a lateral phase separation into a pure lipid phase and a fluid cyclodextrin-rich phase (L(CD)) with reduced acyl chain order parameters, as observed with a derivative containing a cholesterol anchor (M. Roux, R. Auzely-Velty, F. Djedaïni-Pilard, and B. Perly. 2002. Biophysical Journal, 8:813-822). We present another class of amphiphilic cyclodextrins obtained by grafting aspartic acid esterified by two lauryl chains on the oligosaccharide core via a succinyl spacer. The obtained dilauryl-beta-cyclodextrin (betaDLC) was inserted in chain perdeuterated dimyristoylphosphatidylcholine (DMPC-d54) membranes and studied by deuterium NMR ((2)H-NMR). A laterally segregated mixed phase was found to sequester three times more lipids than the cholesteryl derivative (approximately 4-5 lipids per monomer of betaDLC), and a quasipure L(CD) phase could be obtained with a 20% molar concentration of betaDLC. When cooled below the main fluid-to-gel transition of DMPC-d54 the betaDLC-rich phase stays fluid, coexisting with pure lipid in the gel state, and exhibits a sharp transition to a gel phase with frozen DMPC acyl chains at 12.5 degrees C. No lateral phase separation was observed with partially or fully methylated betaDLC, confirming that the stability of the segregated L(CD) phase was governed through hydrogen-bond-mediated intermolecular interactions between cyclodextrin headgroups at the membrane surface. As opposed to native betaDLC, the methylated derivatives were found to strongly increase the orientational order of DMPC acyl chains as the temperature reaches the membrane fluid-to-gel transition. The results are discussed in relation to the "anomalous swelling" of saturated phosphatidylcholine multilamellar membranes known to occur in the vicinity of the main fluid-to-gel transition.

Indexed as

beta-CyclodextrinsBiophysicsCell MembraneCholesterolCyclodextrinsDimyristoylphosphatidylcholineHydrogen BondingLipidsMagnetic Resonance SpectroscopyMethylationModels, ChemicalMolecular ConformationPhosphatidylcholinesSurface PropertiesTemperaturebeta-CyclodextrinsCholesterolCyclodextrinsDimyristoylphosphatidylcholineLipidsPhosphatidylcholines

Identifiers

PMID17496041
PMCPMC1948046
OpenAlexW1982863820

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.