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PMID: 7706316 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Microtubule-associated protein/microtubule affinity-regulating kinase (p110mark). A novel protein kinase that regulates tau-microtubule interactions and dynamic instability by phosphorylation at the Alzheimer-specific site serine 262.

The Journal of biological chemistry ·Vol. 270 ·No. 13 ·1995-03-31 ·Pages 7679-88

Drewes G, Trinczek B, Illenberger S, Biernat J, Schmitt-Ulms G, Meyer HE, Mandelkow EM, Mandelkow E

Abstract

Aberrant phosphorylation of the microtubule-associated protein tau is one of the pathological features of neuronal degeneration in Alzheimer's disease. The phosphorylation of Ser-262 within the microtubule binding region of tau is of particular interest because so far it is observed only in Alzheimer's disease (Hasegawa, M., Morishima-Kawashima, M., Takio, K., Suzuki, M., Titani, K., and Ihara, Y. (1992) J. Biol. Chem. 26, 17047-17054) and because phosphorylation of this site alone dramatically reduces the affinity for microtubules in vitro (Biernat, J., Gustke, N., Drewes, G., Mandelkow, E.-M., and Mandelkow, E. (1993) Neuron 11, 153-163). Here we describe the purification and characterization of a protein-serine kinase from brain tissue with an apparent molecular mass of 110 kDa on SDS gels. This kinase specifically phosphorylates tau on its KIGS or KCGS motifs in the repeat domain, whereas no significant phosphorylation outside this region was detected. Phosphorylation occurs mainly on Ser-262 located in the first repeat. This largely abolishes tau's binding to microtubules and makes them dynamically unstable, in contrast to other protein kinases that phosphorylate tau at or near the repeat domain. The data suggest a role for this novel kinase in cellular events involving rearrangement of the microtuble-associated proteins/microtubule arrays and their pathological degeneration in Alzheimer's disease.

MeSH Terms
Alzheimer Disease/metabolism Amino Acid Sequence Animals Brain/enzymology Chromatography, Ion Exchange Cloning, Molecular Escherichia coli Humans Kinetics Microtubules/metabolism Molecular Sequence Data Peptide Fragments/chemistry,isolation & purification Peptide Mapping Phosphopeptides/chemistry,isolation & purification Phosphorylation Phosphoserine/analysis Protein Serine-Threonine Kinases/isolation & purification,metabolism Recombinant Proteins/biosynthesis,isolation & purification,metabolism Serine Swine Trypsin Tubulin/isolation & purification,metabolism tau Proteins/biosynthesis,isolation & purification,metabolism
Chemicals
Peptide Fragments Phosphopeptides Recombinant Proteins Tubulin tau Proteins Phosphoserine Serine MARK1 protein, human Protein Serine-Threonine Kinases Trypsin
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Drewes G
Max-Planck Unit for Structural Molecular Biology, Hamburg, Federal Republic of Germany.
Trinczek B
Illenberger S
Biernat J
Schmitt-Ulms G
Meyer H E
Mandelkow E M
Mandelkow E
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1995-03-31
Pages
7679-88
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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