Myelin organization in the nodal, paranodal, and juxtaparanodal regions revealed by scanning x-ray microdiffraction

X-ray diffraction has provided extensive information about the arrangement of lipids and proteins in multilamellar myelin. This information has been limited to the abundant inter-nodal regions of the sheath because these regions dominate the scattering when x-ray beams of 100 µm diameter or more are...

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Veröffentlicht in:PloS one 2014-07, Vol.9 (7), p.e100592-e100592
Hauptverfasser: Inouye, Hideyo, Liu, Jiliang, Makowski, Lee, Palmisano, Marilena, Burghammer, Manfred, Riekel, Christian, Kirschner, Daniel A
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container_title PloS one
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creator Inouye, Hideyo
Liu, Jiliang
Makowski, Lee
Palmisano, Marilena
Burghammer, Manfred
Riekel, Christian
Kirschner, Daniel A
description X-ray diffraction has provided extensive information about the arrangement of lipids and proteins in multilamellar myelin. This information has been limited to the abundant inter-nodal regions of the sheath because these regions dominate the scattering when x-ray beams of 100 µm diameter or more are used. Here, we used a 1 µm beam, raster-scanned across a single nerve fiber, to obtain detailed information about the molecular architecture in the nodal, paranodal, and juxtaparanodal regions. Orientation of the lamellar membrane stacks and membrane periodicity varied spatially. In the juxtaparanode-internode, 198-202 Å-period membrane arrays oriented normal to the nerve fiber axis predominated, whereas in the paranode-node, 205-208 Å-period arrays oriented along the fiber direction predominated. In parts of the sheath distal to the node, multiple sets of lamellar reflections were observed at angles to one another, suggesting that the myelin multilayers are deformed at the Schmidt-Lanterman incisures. The calculated electron density of myelin in the different regions exhibited membrane bilayer profiles with varied electron densities at the polar head groups, likely due to different amounts of major myelin proteins (P0 glycoprotein and myelin basic protein). Scattering from the center of the nerve fibers, where the x-rays are incident en face (perpendicular) to the membrane planes, provided information about the lateral distribution of protein. By underscoring the heterogeneity of membrane packing, microdiffraction analysis suggests a powerful new strategy for understanding the underlying molecular foundation of a broad spectrum of myelinopathies dependent on local specializations of myelin structure in both the PNS and CNS.
doi_str_mv 10.1371/journal.pone.0100592
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subjects Analysis
Angle of reflection
Animals
Architectural engineering
Beams (radiation)
Biology
Biology and Life Sciences
Cell Membrane - chemistry
Cell Membrane - metabolism
Central nervous system
Computer engineering
Deformation
Electron density
Fibers
Glycoproteins
Life Sciences
Lipids
Medicine and Health Sciences
Membranes
Mice
Multilayers
Myelin
Myelin basic protein
Myelin Basic Protein - chemistry
Myelin Basic Protein - metabolism
Myelin P0 protein
Myelin P0 Protein - chemistry
Myelin P0 Protein - metabolism
Myelin proteins
Myelin Sheath - chemistry
Myelin Sheath - metabolism
Nervous system
Periodicity
Phospholipids
Proteins
Raster scanning
Research and analysis methods
Scattering
Studies
X-Ray Diffraction
Xenopus laevis
title Myelin organization in the nodal, paranodal, and juxtaparanodal regions revealed by scanning x-ray microdiffraction
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