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Membrane Association Landscape of Myelin Basic Protein Portrays Formation of the Myelin Major Dense Line
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)...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504075/ https://www.ncbi.nlm.nih.gov/pubmed/28694532 http://dx.doi.org/10.1038/s41598-017-05364-3 |
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author | Raasakka, Arne Ruskamo, Salla Kowal, Julia Barker, Robert Baumann, Anne Martel, Anne Tuusa, Jussi Myllykoski, Matti Bürck, Jochen Ulrich, Anne S. Stahlberg, Henning Kursula, Petri |
author_facet | Raasakka, Arne Ruskamo, Salla Kowal, Julia Barker, Robert Baumann, Anne Martel, Anne Tuusa, Jussi Myllykoski, Matti Bürck, Jochen Ulrich, Anne S. Stahlberg, Henning Kursula, Petri |
author_sort | Raasakka, Arne |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5504075 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55040752017-07-12 Membrane Association Landscape of Myelin Basic Protein Portrays Formation of the Myelin Major Dense Line Raasakka, Arne Ruskamo, Salla Kowal, Julia Barker, Robert Baumann, Anne Martel, Anne Tuusa, Jussi Myllykoski, Matti Bürck, Jochen Ulrich, Anne S. Stahlberg, Henning Kursula, Petri Sci Rep Article 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. Nature Publishing Group UK 2017-07-10 /pmc/articles/PMC5504075/ /pubmed/28694532 http://dx.doi.org/10.1038/s41598-017-05364-3 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Raasakka, Arne Ruskamo, Salla Kowal, Julia Barker, Robert Baumann, Anne Martel, Anne Tuusa, Jussi Myllykoski, Matti Bürck, Jochen Ulrich, Anne S. Stahlberg, Henning Kursula, Petri Membrane Association Landscape of Myelin Basic Protein Portrays Formation of the Myelin Major Dense Line |
title | Membrane Association Landscape of Myelin Basic Protein Portrays Formation of the Myelin Major Dense Line |
title_full | Membrane Association Landscape of Myelin Basic Protein Portrays Formation of the Myelin Major Dense Line |
title_fullStr | Membrane Association Landscape of Myelin Basic Protein Portrays Formation of the Myelin Major Dense Line |
title_full_unstemmed | Membrane Association Landscape of Myelin Basic Protein Portrays Formation of the Myelin Major Dense Line |
title_short | Membrane Association Landscape of Myelin Basic Protein Portrays Formation of the Myelin Major Dense Line |
title_sort | membrane association landscape of myelin basic protein portrays formation of the myelin major dense line |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504075/ https://www.ncbi.nlm.nih.gov/pubmed/28694532 http://dx.doi.org/10.1038/s41598-017-05364-3 |
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