Journal of Biological Chemistry · 1995 · 558 citations · 68 references
Life SciencesBiochemistryMolecular BiologyMolecular NeurobiologyProtein BiochemistryProteomicsMass Spectrometry-based ProteomicsPeptide AnalysisProtein PhosphorylationProtein Sequence AnalysisTau PathologyMass Spectrometry-based Phosphorylation AnalysisPhosphopeptide IdentificationPhosphorylation Site MappingPost-translationally Modified PeptidesProtein Phosphorylation AnalysisProtein Phosphosite MappingTau Hyperphosphorylation
To gain insight into the abnormal phosphorylation of PHF-tau, we have determined the phosphorylation sites by identifying phosphopeptides by means of ion spray mass spectrometry followed by sequencing of ethane-thiol-modified peptides. Nineteen sites have been identified; all but Ser-262 are localized to the amino- and carboxyl-terminal flanking regions of the microtubule-binding domain. Eleven sites correspond to fetal type sites. Unexpectedly, 10 are non-proline-directed, whereas the others are proline-directed. Thus, the abnormal phosphorylation of PHF-tau can be considered to consist of fetal type phosphorylation and additional proline-directed and non-proline-directed phosphorylation. This non-fetal type phosphorylation may provide PHF-tau with the unusual characteristics.
68
A protein factor essential for microtubule assembly.
Murray Weingarten, Arthur H. Lockwood, S Y Hwo et al. · Proceedings of the National Academy of Sciences · 1975 · 3.1K citations · Full text
A68: a Major Subunit of Paired Helical Filaments and Derivatized Forms of Normal Tau
Virginia M.‐Y. Lee, Brian J. Balin, László Ötvös et al. · Science · 1991 · 1.4K citations