Ion Mobility‐Enhanced Data‐Independent Acquisitions Enable a Deep Proteomic Landscape of Oligodendrocytes

• Published in: Proteomics (Weinheim) Vol. 17; no. 21
• Main Authors: Cassoli, Juliana S., Brandão‐Teles, Caroline, Santana, Aline G., Souza, Gustavo H. M. F., Martins‐de‐Souza, Daniel
• Format: Journal Article
• Language: English
• Published: Germany Wiley Subscription Services, Inc 01.11.2017
• Subjects: Axonogenesis; Axons; Biological activity; Cell Proliferation; Cells, Cultured; Central nervous system; Data acquisition; data‐independent acquisitions; Energy metabolism; Flow rates; Fractionation; Gene Expression Regulation, Developmental; Glia; Humans; Insulation; ion mobility; Ionic mobility; Maturation; Metabolism; Mobility; Myelination; Neurogenesis; Neuroglia; Oligodendrocytes; Oligodendroglia - cytology; Oligodendroglia - metabolism; Peptides; Proteins; Proteome - analysis; Spectrometry, Mass, Electrospray Ionization - methods; UDMSE; ion mobility; oligodendrocytes; data-independent acquisitions; UDMSE
• ISSN: 1615-9853; 1615-9861; 1615-9861
• DOI: 10.1002/pmic.201700209

Oligodendrocytes are a type of neuroglia that provide trophic support and insulation to axons in the central nervous system. The genesis and maturation of oligodendrocytes are essential processes for myelination and the course of CNS development. Using ion mobility‐enhanced, data‐independent acquisitions and 2D‐nanoUPLC fractionation operating at nanoscale flow rates, we established a comprehensive data set of proteins expressed by the human oligodendroglia cell line MO3.13. The final dataset incorporating all fractions comprised 223 531 identified peptides assigned to 10 390 protein hits, an improvement of 4.5 times on identified proteins described previously by our group using the same cell line. Identified proteins play pivotal roles in many biological processes such as cell growth and development and energy metabolism, providing a rich resource for future studies on oligodendrocyte development, myelination, axonal support, and the regulation of such process. Our results can help further studies that use MO3.13 cells as a tool of investigation, not only in relation to oligodendrocyte maturation, but also to diseases that have oligodendrocytes as key players. All MS data have been deposited in the ProteomeXchange with identifier PXD004696.