Shaping membrane interfaces in lipid vesicles mimicking the cytoplasmic leaflet of myelin through variation of cholesterol and myelin basic protein contents.

Dynamic light scattering Electron paramagnetic resonance Intrinsically disordered protein (IDP) Transmission electron microscopy

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:
10 2023
Historique:
received: 08 12 2022
revised: 23 04 2023
accepted: 20 05 2023
medline: 14 8 2023
pubmed: 28 5 2023
entrez: 27 5 2023
Statut: ppublish

Résumé

Myelin basic protein (MBP) is an intrinsically disordered protein and in the central nervous system (CNS) mainly responsible for connecting the cytoplasmic surfaces of the multilamellar, compact myelin. Increased posttranslational modification of MBP is linked to both, the natural development (from adolescent to adult brains) of myelin, and features of multiple sclerosis. Here, we study how a combination of this intrinsically disordered myelin protein with varying the natural cholesterol content may alter the characteristics of myelin-like membranes and interactions between these membranes. Large unilamellar vesicles (LUVs) with a composition mimicking the cytoplasmic leaflet of myelin were chosen as the model system, in which different parameters contributing to the interactions between the lipid membrane and MBP were investigated. While we use cryo-transmission electron microscopy (TEM) for imaging, dynamic light scattering (DLS) and electrophoretic measurements through continuously-monitored phase-analysis light scattering (cmPALS) were used for a more global overview of particle size and charge, and electron paramagnetic resonance (EPR) spectroscopy was utilized for local behavior of lipids in the vesicles' membranes in aqueous solution. The cholesterol content was varied from 060 % in these LUVs and measurements were performed in the presence and absence of MBP. We find that the composition of the lipid layers is relevant to the interaction with MBP. Not only the size, the shape and the aggregation behavior of the vesicles depend on the cholesterol content, but also within each membrane, cholesterol's freedom of movement, its environmental polarity and its distribution were found to depend on the content using the EPR-active spin-labeled cholesterol (CSOSL). In addition, DLS and EPR measurements probing the transition temperatures of the lipid phases allow a correlation of specific behavior with the human body temperature of 37 °C. Overall, our results aid in understanding the importance of the native cholesterol content in the healthy myelin membrane, which serves as the basis for stable and optimum protein-bilayer interactions. Although studied in this specific myelin-like system, from a more general and materials science-oriented point of view, we could establish how membrane and vesicle properties depend on cholesterol and/or MBP content, which might be useful generally when specific membrane and vesicle characteristics are sought for.

Identifiants

pubmed: 37244538
pii: S0005-2736(23)00061-5
doi: 10.1016/j.bbamem.2023.184179
pii:
doi:

Substances chimiques

Myelin Basic Protein 0
Unilamellar Liposomes 0
Lipids 0
Cholesterol 97C5T2UQ7J

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

184179

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Dariush Hinderberger reports financial support was provided by German Research Foundation. George Harauz reports financial support was provided by Natural Sciences and Engineering Research Council of Canada.

Auteurs

Jennica Träger (J)

Institute of Chemistry, Physical Chemistry - Complex Self-organizing Systems, Martin-Luther-Universität Halle-Wittenberg, Halle (Saale), Saxony-Anhalt, Germany; Interdisciplinary Research Center HALOmem at the Martin-Luther-Universität Halle-Wittenberg, Germany.

Annette Meister (A)

Interdisciplinary Research Center HALOmem at the Martin-Luther-Universität Halle-Wittenberg, Germany; Institute of Biochemistry, Physical Biotechnology, Martin-Luther-Universität Halle-Wittenberg, Halle (Saale), Germany.

Gerd Hause (G)

Biocenter, Martin-Luther-Universität Halle-Wittenberg, Halle (Saale), Germany.

George Harauz (G)

Department of Molecular and Cellular Biology, University of Guelph, Guelph, Ontario, Canada.

Dariush Hinderberger (D)

Institute of Chemistry, Physical Chemistry - Complex Self-organizing Systems, Martin-Luther-Universität Halle-Wittenberg, Halle (Saale), Saxony-Anhalt, Germany; Interdisciplinary Research Center HALOmem at the Martin-Luther-Universität Halle-Wittenberg, Germany. Electronic address: dariush.hinderberger@chemie.uni-halle.de.

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Classifications MeSH