A conformation- and phosphorylation-dependent antibody recognizing the paired helical filaments of Alzheimer's disease

Gregory A. Jicha, Eric Lane, Inez Vincent, Laszlo Otvos, Ralf Hoffmann, Peter Davies

Research output: Contribution to journalArticlepeer-review

224 Scopus citations

Abstract

Hyperphosphorylated tau (PHF-tau) is the major constituent of paired helical filaments (PHFs) from Alzheimer's disease (AD) brains. This conclusion has been based largely on the creation and characterization of monoclonal antibodies raised against PHFs, which can be classified in three categories: (a) those recognizing unmodified primary sequences of tau, (b) those recognizing phosphorylation-dependent epitopes on tau, and (c) those recognizing conformation-dependent epitopes on tau. Recent studies have suggested that the antibodies recognizing primary sequence and phosphorylation-dependent epitopes on tau are unable to distinguish between normal adult biopsy tau and PHF-tau. We now present evidence for a new fourth class, of monoclonal antibodies recognizing conformation-dependent phosphoepitopes on tau, typified by TG-3, a monoclonal antibody raised to PHFs from AD brain homogenates. Studies using a series of deletional tau mutants, site-directed tau mutants, and synthetic peptides enable the precise epitope mapping of TG-3. Additional studies demonstrate that TG-3 reacts with neonatal mouse tau and PHF-tau but does not recognize adult mouse tau or tau derived from normal human autopsy or biopsy tissue. Further investigation reveals that TG-3 recognizes a unique conformation of tau found almost exclusively in PHFs from AD brains.

Original languageEnglish
Pages (from-to)2087-2095
Number of pages9
JournalJournal of Neurochemistry
Volume69
Issue number5
DOIs
StatePublished - Nov 1997

Keywords

  • Alzheimer's disease
  • Conformation
  • Epitope
  • Paired helical filaments
  • Phosphorylation
  • Tau

ASJC Scopus subject areas

  • Biochemistry
  • Cellular and Molecular Neuroscience

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