Cargando…
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...
Autores principales: | , , , , , , , , |
---|---|
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 |
_version_ | 1783577879248896000 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7466725 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT jahnolaf thecnsmyelinproteomedeepprofileandpersistenceafterpostmortemdelay AT siemssophieb thecnsmyelinproteomedeepprofileandpersistenceafterpostmortemdelay AT kuschkathrin thecnsmyelinproteomedeepprofileandpersistenceafterpostmortemdelay AT hessedorte thecnsmyelinproteomedeepprofileandpersistenceafterpostmortemdelay AT jungramonab thecnsmyelinproteomedeepprofileandpersistenceafterpostmortemdelay AT liepoldthomas thecnsmyelinproteomedeepprofileandpersistenceafterpostmortemdelay AT ueckermarina thecnsmyelinproteomedeepprofileandpersistenceafterpostmortemdelay AT sunting thecnsmyelinproteomedeepprofileandpersistenceafterpostmortemdelay AT wernerhaukeb thecnsmyelinproteomedeepprofileandpersistenceafterpostmortemdelay AT jahnolaf cnsmyelinproteomedeepprofileandpersistenceafterpostmortemdelay AT siemssophieb cnsmyelinproteomedeepprofileandpersistenceafterpostmortemdelay AT kuschkathrin cnsmyelinproteomedeepprofileandpersistenceafterpostmortemdelay AT hessedorte cnsmyelinproteomedeepprofileandpersistenceafterpostmortemdelay AT jungramonab cnsmyelinproteomedeepprofileandpersistenceafterpostmortemdelay AT liepoldthomas cnsmyelinproteomedeepprofileandpersistenceafterpostmortemdelay AT ueckermarina cnsmyelinproteomedeepprofileandpersistenceafterpostmortemdelay AT sunting cnsmyelinproteomedeepprofileandpersistenceafterpostmortemdelay AT wernerhaukeb cnsmyelinproteomedeepprofileandpersistenceafterpostmortemdelay |