Hostname: page-component-586b7cd67f-dlnhk Total loading time: 0 Render date: 2024-11-24T16:26:07.805Z Has data issue: false hasContentIssue false

Electron Microscopy of Myelin Basic Protein (MBP) Organized as Planar Arrays on a Lipid Monolayer Surface: Deimination of MBP Hinders Its Organizational Properties

Published online by Cambridge University Press:  02 July 2020

N. Ishiyama
Affiliation:
Molecular Biology and Genetics, University of Guelph, Guelph, Canada, NIG 2W1.
P. Matharu
Affiliation:
Pathology and Microbiology, University of Bristol, Bristol, UK, BS8 1TD.
I.R. Bates
Affiliation:
Molecular Biology and Genetics, University of Guelph, Guelph, Canada, NIG 2W1.
D.D. Wood
Affiliation:
Structural Biology and Biochemistry, Hospital for Sick Children, Toronto, Canada, M5G 1X6.
M.A. Moscarello
Affiliation:
Structural Biology and Biochemistry, Hospital for Sick Children, Toronto, Canada, M5G 1X6.
N.J. Viner
Affiliation:
Pathology and Microbiology, University of Bristol, Bristol, UK, BS8 1TD.
G. Harauz
Affiliation:
Molecular Biology and Genetics, University of Guelph, Guelph, Canada, NIG 2W1.
Get access

Extract

Myelin basic protein (MBP) is one of the principal constituents of the mammalian myelin sheath. It is a basic peripheral membrane protein in the major dense line and is believed to play a structural role in maintaining myelin stability through its close association with lipids and other proteins. Immune responses to MBP have been implicated in the pathogenesis of multiple sclerosis (MS), the most common autoimmune disease of the central nervous system in North America and Northern Europe. The correlation between the severity of MS and the deimination of arginyl to citrullinyl residues in MBP was well illustrated in the acute case of MS (Marburg type) that contained MBP with 18 out of 19 arginines citrullinated.

We have studied a recombinant hexahistidine-tagged murine MBP (rmMBP, 18.5 kDa isoform) by electron microscopy of the protein organized as planar arrays on lipid monolayers that consisted of the nickel chelating lipid, l,2-dioleoyl-.yn-glycero-3-[(N(5-amino-l-carboxypentyl)iminodiacetic acid)succinyl] (Nickel salt) (Ni2+-NTADOGS), and the filler lipid, liver phosphatidylinositol (PI).

Type
Electron Cryomicroscopy of Macromolecules
Copyright
Copyright © Microscopy Society of America

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

l.Wood, D.D. etal. Ann. Neurol. 40(1996) 1824.CrossRefGoogle Scholar
2.Beniac, D.R. et al. J. Struct. Biol., in press, 2000.Google Scholar
3.Kubalek, E.W. et al. J. Struct. Biol. 113 (1994) 117123.CrossRefGoogle Scholar
4.Taylor, K.A. and Taylor, D.W.. J. Struct. Biol. 128 (1999) 7581.CrossRefGoogle Scholar
5.Napolitano, L. et al. J. Cell Biol. 34 (1967) 817826.CrossRefGoogle Scholar
6. This work was supported by the Canadian MRC, NSERC, and Multiple Sclerosis Society, and by the Wellcome Trust.Google Scholar