Myelin: Methods for Purification and Proteome Analysis.
Cholesterol
Cyclic nucleotide phosphodiesterase (CNP)
Demyelination
Density gradient ultracentrifugation
Lipidome/lipidomics
Mass spectrometry
Myelin
Myelin basic protein (MBP)
Nerve conduction
Oligodendrocyte
Proteoform
Proteolipid protein (PLP)
Proteome/proteomics
Transcriptome/transcriptomics
White matter
Journal
Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969
Informations de publication
Date de publication:
2019
2019
Historique:
entrez:
2
3
2019
pubmed:
2
3
2019
medline:
3
7
2019
Statut:
ppublish
Résumé
Molecular characterization of myelin is a prerequisite for understanding the normal structure of the axon/myelin-unit in the healthy nervous system and abnormalities in myelin-related disorders. However, reliable molecular profiles necessitate very pure myelin membranes, in particular when considering the power of highly sensitive "omics"-data acquisition methods. Here, we recapitulate the history and recent applications of myelin purification. We then provide our laboratory protocols for the biochemical isolation of a highly pure myelin-enriched fraction from mouse brains and for its proteomic analysis. We also supply methodological modifications when investigating posttranslational modifications, RNA, or myelin from peripheral nerves. Notably, technical advancements in solubilizing myelin are beneficial for gel-based and gel-free myelin proteome analyses. We conclude this article by exemplifying the exceptional power of label-free proteomics in the mass-spectrometric quantification of myelin proteins.
Identifiants
pubmed: 30820892
doi: 10.1007/978-1-4939-9072-6_3
doi:
Substances chimiques
Myelin Proteins
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM