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The CNS Myelin Proteome: Deep Profile and Persistence After Post-mortem Delay

Myelin membranes are dominated by lipids while the complexity of their protein composition has long been considered to be low. However, numerous additional myelin proteins have been identified since. Here we revisit the proteome of myelin biochemically purified from the brains of healthy c56Bl/6N-mi...

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Autores principales: Jahn, Olaf, Siems, Sophie B., Kusch, Kathrin, Hesse, Dörte, Jung, Ramona B., Liepold, Thomas, Uecker, Marina, Sun, Ting, Werner, Hauke B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7466725/
https://www.ncbi.nlm.nih.gov/pubmed/32973451
http://dx.doi.org/10.3389/fncel.2020.00239
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author Jahn, Olaf
Siems, Sophie B.
Kusch, Kathrin
Hesse, Dörte
Jung, Ramona B.
Liepold, Thomas
Uecker, Marina
Sun, Ting
Werner, Hauke B.
author_facet Jahn, Olaf
Siems, Sophie B.
Kusch, Kathrin
Hesse, Dörte
Jung, Ramona B.
Liepold, Thomas
Uecker, Marina
Sun, Ting
Werner, Hauke B.
author_sort Jahn, Olaf
collection PubMed
description Myelin membranes are dominated by lipids while the complexity of their protein composition has long been considered to be low. However, numerous additional myelin proteins have been identified since. Here we revisit the proteome of myelin biochemically purified from the brains of healthy c56Bl/6N-mice utilizing complementary proteomic approaches for deep qualitative and quantitative coverage. By gel-free, label-free mass spectrometry, the most abundant myelin proteins PLP, MBP, CNP, and MOG constitute 38, 30, 5, and 1% of the total myelin protein, respectively. The relative abundance of myelin proteins displays a dynamic range of over four orders of magnitude, implying that PLP and MBP have overshadowed less abundant myelin constituents in initial gel-based approaches. By comparisons with published datasets we evaluate to which degree the CNS myelin proteome correlates with the mRNA and protein abundance profiles of myelin and oligodendrocytes. Notably, the myelin proteome displays only minor changes if assessed after a post-mortem delay of 6 h. These data provide the most comprehensive proteome resource of CNS myelin so far and a basis for addressing proteomic heterogeneity of myelin in mouse models and human patients with white matter disorders.
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spelling pubmed-74667252020-09-23 The CNS Myelin Proteome: Deep Profile and Persistence After Post-mortem Delay Jahn, Olaf Siems, Sophie B. Kusch, Kathrin Hesse, Dörte Jung, Ramona B. Liepold, Thomas Uecker, Marina Sun, Ting Werner, Hauke B. Front Cell Neurosci Neuroscience Myelin membranes are dominated by lipids while the complexity of their protein composition has long been considered to be low. However, numerous additional myelin proteins have been identified since. Here we revisit the proteome of myelin biochemically purified from the brains of healthy c56Bl/6N-mice utilizing complementary proteomic approaches for deep qualitative and quantitative coverage. By gel-free, label-free mass spectrometry, the most abundant myelin proteins PLP, MBP, CNP, and MOG constitute 38, 30, 5, and 1% of the total myelin protein, respectively. The relative abundance of myelin proteins displays a dynamic range of over four orders of magnitude, implying that PLP and MBP have overshadowed less abundant myelin constituents in initial gel-based approaches. By comparisons with published datasets we evaluate to which degree the CNS myelin proteome correlates with the mRNA and protein abundance profiles of myelin and oligodendrocytes. Notably, the myelin proteome displays only minor changes if assessed after a post-mortem delay of 6 h. These data provide the most comprehensive proteome resource of CNS myelin so far and a basis for addressing proteomic heterogeneity of myelin in mouse models and human patients with white matter disorders. Frontiers Media S.A. 2020-08-19 /pmc/articles/PMC7466725/ /pubmed/32973451 http://dx.doi.org/10.3389/fncel.2020.00239 Text en Copyright © 2020 Jahn, Siems, Kusch, Hesse, Jung, Liepold, Uecker, Sun and Werner. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Jahn, Olaf
Siems, Sophie B.
Kusch, Kathrin
Hesse, Dörte
Jung, Ramona B.
Liepold, Thomas
Uecker, Marina
Sun, Ting
Werner, Hauke B.
The CNS Myelin Proteome: Deep Profile and Persistence After Post-mortem Delay
title The CNS Myelin Proteome: Deep Profile and Persistence After Post-mortem Delay
title_full The CNS Myelin Proteome: Deep Profile and Persistence After Post-mortem Delay
title_fullStr The CNS Myelin Proteome: Deep Profile and Persistence After Post-mortem Delay
title_full_unstemmed The CNS Myelin Proteome: Deep Profile and Persistence After Post-mortem Delay
title_short The CNS Myelin Proteome: Deep Profile and Persistence After Post-mortem Delay
title_sort cns myelin proteome: deep profile and persistence after post-mortem delay
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7466725/
https://www.ncbi.nlm.nih.gov/pubmed/32973451
http://dx.doi.org/10.3389/fncel.2020.00239
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