Temperature dependent self-organization of DMPC membranes promoted by intermediate amounts of the saponin aescin.


Journal

Biochimica et biophysica acta. Biomembranes
ISSN: 1879-2642
Titre abrégé: Biochim Biophys Acta Biomembr
Pays: Netherlands
ID NLM: 101731713

Informations de publication

Date de publication:
01 05 2019
Historique:
received: 11 09 2018
revised: 18 12 2018
accepted: 28 01 2019
pubmed: 9 2 2019
medline: 27 11 2019
entrez: 9 2 2019
Statut: ppublish

Résumé

The plant-derived biosurfactant aescin is naturally present in many plants and is used for treatment of disorders such as varicose veins and inflammation of veins. The hemolytic activity of this saponin is attributed to its interaction with cholesterol in the red blood cell membrane. This work investigates the phase and aggregation behavior of saponin-containing model membranes consisting of the phospholipid 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC). The aescin concentrations studied range from 1 mol% to 7 mol% with respect to the total lipid content. The methods of choice to elucidate the structural picture are small-angle scattering of X-rays (SAXS) and neutrons (SANS) and cryogenic transmission electron microscopy (cryo-TEM). SANS and SAXS revealed that at lower aescin contents vesicular structures are conserved and vesicles tend to aggregate already at aescin contents of around 1 mol%. Aggregation and vesicle deformation effects are found to be stronger when the phospholipids are in the L [Formula: see text] phase. With increasing aescin content, mixed structures, i.e. aggregated and deformed vesicles and solubilized bilayer fragments, are present. This was proven for a sample with 4 mol% aescin by cryo-TEM. An increasing aescin amount leads to membrane decomposition and free standing bilayers which tend to build stacks at high temperature. These stacks are characterized by SAXS using the modified Caillé theory. Analyses and model dependent fitting reveal formation of well-defined structures beginning at 7 mol% aescin.

Identifiants

pubmed: 30735626
pii: S0005-2736(19)30026-4
doi: 10.1016/j.bbamem.2019.01.015
pii:
doi:

Substances chimiques

Membranes, Artificial 0
Escin 6805-41-0
Dimyristoylphosphatidylcholine U86ZGC74V5

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

897-906

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

Ramsia Sreij (R)

Physical and Biophysical Chemistry, Bielefeld University, Universitätsstr. 25, 33615 Bielefeld, Germany.

Carina Dargel (C)

Physical and Biophysical Chemistry, Bielefeld University, Universitätsstr. 25, 33615 Bielefeld, Germany.

Yvonne Hannappel (Y)

Physical and Biophysical Chemistry, Bielefeld University, Universitätsstr. 25, 33615 Bielefeld, Germany.

Jacques Jestin (J)

Laboratoire Léon Brillouin, UMR12 CEA-CNRS, Gif sur Yvette Cedex 91191, France.

Sylvain Prévost (S)

ESRF-The European Synchrotron Radiation Facility, 71 Avenue des Martyrs, 38043 Grenoble Cedex 9, France; Institut Laue-Langevin, DS/LSS, 71 avenue des Martyrs, Grenoble Cedex 9 38042, France.

Rajeev Dattani (R)

ESRF-The European Synchrotron Radiation Facility, 71 Avenue des Martyrs, 38043 Grenoble Cedex 9, France.

Oliver Wrede (O)

Physical and Biophysical Chemistry, Bielefeld University, Universitätsstr. 25, 33615 Bielefeld, Germany.

Thomas Hellweg (T)

Physical and Biophysical Chemistry, Bielefeld University, Universitätsstr. 25, 33615 Bielefeld, Germany. Electronic address: thomas.hellweg@uni-bielefeld.de.

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Classifications MeSH