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440-kD ankyrinB: structure of the major developmentally regulated domain and selective localization in unmyelinated axons.

Publication ,  Journal Article
Chan, W; Kordeli, E; Bennett, V
Published in: J Cell Biol
December 1993

440-kD ankyrinB is an alternatively spliced variant of 220-kD ankyrinB, with a predicted 220-kD sequence inserted between the membrane/spectrin binding domains and COOH-terminal domain (Kunimoto, M., E. Otto, and V. Bennett. 1991. J. Cell Biol. 236:1372-1379). This paper presents the sequence of 2085 amino acids comprising the alternatively spliced portion of 440-kD ankyrinB, and provides evidence that much of the inserted sequence has the configuration of an extended random coil. Notable features of the inserted sequence include a hydrophilicity profile that contains few hydrophobic regions, and 220 predicted sites for phosphorylation by protein kinases (casein kinase 2, protein kinase C, and proline-directed protein kinase). Secondary structure and folding of the inserted amino acid residues were deduced from properties of recombinant polypeptides. Frictional ratios of 1.9-2.4 were calculated from Stokes radii and sedimentation coefficients, for polypeptides comprising 70% of the inserted sequence, indicating a highly asymmetric shape. Circular dichroism spectra of these polypeptides indicate a nonglobular structure with negligible alpha-helix or beta sheet folding. These results suggest a ball-and-chain model for 440-kD ankyrinB with a membrane-associated globular head domain and an extended filamentous tail domain encoded by the inserted sequence. Immunofluorescence and immunoblot studies of developing neonatal rat optic nerve indicate that 440-kD ankyrinB is selectively targeted to premyelinated axons, and that 440-kD ankyrinB disappears from these axons coincident with myelination. Hypomyelinated nerve tracts of the myelin-deficient Shiverer mice exhibit elevated levels of 440-kD ankyrinB. 440-kD ankyrinB thus is a specific component of unmyelinated axons and expression of 440-kD ankyrinB may be downregulated as a consequence of myelination.

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Published In

J Cell Biol

DOI

ISSN

0021-9525

Publication Date

December 1993

Volume

123

Issue

6 Pt 1

Start / End Page

1463 / 1473

Location

United States

Related Subject Headings

  • Structure-Activity Relationship
  • Solubility
  • Recombinant Proteins
  • Rats
  • Protein Structure, Secondary
  • Optic Nerve
  • Molecular Sequence Data
  • Mice, Neurologic Mutants
  • Mice
  • Humans
 

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Chan, W., Kordeli, E., & Bennett, V. (1993). 440-kD ankyrinB: structure of the major developmentally regulated domain and selective localization in unmyelinated axons. J Cell Biol, 123(6 Pt 1), 1463–1473. https://doi.org/10.1083/jcb.123.6.1463
Chan, W., E. Kordeli, and V. Bennett. “440-kD ankyrinB: structure of the major developmentally regulated domain and selective localization in unmyelinated axons.J Cell Biol 123, no. 6 Pt 1 (December 1993): 1463–73. https://doi.org/10.1083/jcb.123.6.1463.
Chan, W., et al. “440-kD ankyrinB: structure of the major developmentally regulated domain and selective localization in unmyelinated axons.J Cell Biol, vol. 123, no. 6 Pt 1, Dec. 1993, pp. 1463–73. Pubmed, doi:10.1083/jcb.123.6.1463.

Published In

J Cell Biol

DOI

ISSN

0021-9525

Publication Date

December 1993

Volume

123

Issue

6 Pt 1

Start / End Page

1463 / 1473

Location

United States

Related Subject Headings

  • Structure-Activity Relationship
  • Solubility
  • Recombinant Proteins
  • Rats
  • Protein Structure, Secondary
  • Optic Nerve
  • Molecular Sequence Data
  • Mice, Neurologic Mutants
  • Mice
  • Humans