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PMID: 1560225 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Fetal-type phosphorylation of the tau in paired helical filaments.

Journal of neurochemistry ·Vol. 58 ·No. 5 ·1992-05-00 ·Pages 1667-75

Kanemaru K, Takio K, Miura R, Titani K, Ihara Y

Abstract

To determine the phosphorylation sites of the tau in paired helical filaments (PHF), two types of PHF antisera with different specificities were used: One was a conventional anti-PHF, and the other was an antiserum to formic acid-denatured PHF (anti-HFoPHF). Phosphorylated tau-specific antibodies, anti-ptau 1 and anti-ptau 2, were prepared from anti-PHF and anti-HFoPHF, respectively. We found that both anti-ptau 1 and anti-ptau 2 labeled fetal or juvenile tau but not adult tau. The anti-ptau 1- and anti-ptau 2-recognition sites were immunochemically localized to the fragment Asp313 to Ile328 in the most COOH-terminal portion of tau. Furthermore, Ser315 was determined as the anti-ptau 2 recognition site. The sequence surrounding Ser315 was not found in the canonical sequences phosphorylated with known kinases.

MeSH Terms
Amino Acid Sequence Animals Antibodies/immunology Enzyme-Linked Immunosorbent Assay Fetus/metabolism Humans Immune Sera/immunology Molecular Sequence Data Neurofibrillary Tangles/immunology,metabolism,ultrastructure Phosphorylation Rats tau Proteins/chemistry,metabolism
Chemicals
Antibodies Immune Sera tau Proteins
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Kanemaru K
Department of Neurophysiology, Tokyo Metropolitan Institute of Gerontology, University of Tokyo, Japan.
Takio K
Miura R
Titani K
Ihara Y
Article Info
Journal
Journal of neurochemistry
Abbr.
J Neurochem
ISSN
0022-3042
Published
1992-05-00
Pages
1667-75
Language
English
Region
England
NLM ID
2985190R
Subset
IM
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