Membrane Association Landscape of Myelin Basic Protein Portrays Formation of the Myelin Major Dense Line.
Détails
ID Serval
serval:BIB_873FED5BBBFB
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Membrane Association Landscape of Myelin Basic Protein Portrays Formation of the Myelin Major Dense Line.
Périodique
Scientific reports
ISSN
2045-2322 (Electronic)
ISSN-L
2045-2322
Statut éditorial
Publié
Date de publication
10/07/2017
Peer-reviewed
Oui
Volume
7
Numéro
1
Pages
4974
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: epublish
Publication Status: epublish
Résumé
Compact myelin comprises most of the dry weight of myelin, and its insulative nature is the basis for saltatory conduction of nerve impulses. The major dense line (MDL) is a 3-nm compartment between two cytoplasmic leaflets of stacked myelin membranes, mostly occupied by a myelin basic protein (MBP) phase. MBP is an abundant myelin protein involved in demyelinating diseases, such as multiple sclerosis. The association of MBP with lipid membranes has been studied for decades, but the MBP-driven formation of the MDL remains elusive at the biomolecular level. We employed complementary biophysical methods, including atomic force microscopy, cryo-electron microscopy, and neutron scattering, to investigate the formation of membrane stacks all the way from MBP binding onto a single membrane leaflet to the organisation of a stable MDL. Our results support the formation of an amorphous protein phase of MBP between two membrane bilayers and provide a molecular model for MDL formation during myelination, which is of importance when understanding myelin assembly and demyelinating conditions.
Mots-clé
Animals, Cell Membrane/chemistry, Cell Membrane/metabolism, Cryoelectron Microscopy, Mice, Microscopy, Atomic Force, Models, Molecular, Myelin Basic Protein/chemistry, Myelin Basic Protein/metabolism, Myelin Sheath/chemistry, Myelin Sheath/metabolism, Protein Conformation, Scattering, Small Angle
Pubmed
Web of science
Open Access
Oui
Création de la notice
09/06/2023 15:02
Dernière modification de la notice
08/07/2023 5:50