Myelin basic protein (MBP) charge variants show different sphingomyelin-mediated interactions with myelin-like lipid monolayers.


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 02 2020
Historique:
received: 12 03 2019
revised: 13 08 2019
accepted: 16 09 2019
pubmed: 6 12 2019
medline: 6 5 2020
entrez: 6 12 2019
Statut: ppublish

Résumé

Multiple sclerosis (MS) is correlated with increased deimination of myelin basic protein (MBP) in the central nervous system. Here, the interaction of MBP C1 (charge: +19) and MBP C8 (charge: +13) with the major lipids of the cytoplasmic side of the oligodendrocyte membrane is analysed using monolayer adsorption experiments and epifluorescence microscopy. Our findings show that the electrostatic attraction between the positively charged proteins and negatively charged lipids in the myelin-like monolayers competes with the incorporation of MBP into regions directly bordering cholesterol-rich domains. The latter is favoured to avoid additional lipid condensation and reduction in fluidity of the phospholipid layer. We find that MBP C1 does not incorporate at the cholesterol-rich domains if sphingomyelin (SM) is absent from the lipid composition. In contrast, MBP C8 is still incorporated near cholesterol-enriched regions without SM. Thus, the highly charged C1 variant needs a specific interaction with SM, whereas for C8 the incorporation at the cholesterol-rich regions is ensured due to its reduced net positive charge. This phenomenon may be relevant for the correlation of higher amounts of MBP C8 in brains of adult MS patients and healthy children, in which the amount of SM is reduced compared to healthy adults.

Identifiants

pubmed: 31805269
pii: S0005-2736(19)30223-8
doi: 10.1016/j.bbamem.2019.183077
pii:
doi:

Substances chimiques

Ions 0
Mbp protein, mouse 0
Myelin Basic Protein 0
Phospholipids 0
Sphingomyelins 0
Unilamellar Liposomes 0
Cholesterol 97C5T2UQ7J

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

183077

Informations de copyright

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

Auteurs

Katharina Widder (K)

Institut für Chemie, Martin-Luther-Universität Halle-Wittenberg, Von-Danckelmann-Platz 4, Halle (Saale) 06120, Germany.

George Harauz (G)

Department of Molecular and Cellular Biology, University of Guelph, 50 Stone Road East, Guelph, Ontario N1G 2W1, Canada.

Dariush Hinderberger (D)

Institut für Chemie, Martin-Luther-Universität Halle-Wittenberg, Von-Danckelmann-Platz 4, Halle (Saale) 06120, Germany. Electronic address: dariush.hinderberger@chemie.uni-halle.de.

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Classifications MeSH