Characterization of paired helical filaments by scanning transmission electron microscopy
- 1 July 2005
- journal article
- review article
- Published by Wiley in Microscopy Research and Technique
- Vol. 67 (3-4), 126-140
- https://doi.org/10.1002/jemt.20188
Abstract
Paired helical filaments (PHFs) are abnormal twisted filaments composed of hyperphosphorylated tau protein. They are found in Alzheimer's disease and other neurodegenerative disorders designated as tauopathies. They are a major component of intracellular inclusions known as neurofibrillary tangles (NFTs). The objective of this review is to summarize various structural studies of PHFs in which using scanning transmission electron microscopy (STEM) has been particularly informative. STEM provides shape and mass per unit length measurements important for studying ultrastructural aspects of filaments. These include quantitative comparisons between dispersed and aggregated populations of PHFs as well as comparative studies of PHFs in Alzheimer's disease and other neurodegenerative disorders. Other approaches are also discussed if relevant or complementary to studies using STEM, e.g., application of a novel staining reagent, Nanovan. Our understanding of the PHF structure and the development of PHFs into NFTs is presented from a historical perspective. Others goals are to describe the biochemical and ultrastructural complexity of authentic PHFs, to assess similarities between authentic and synthetic PHFs, and to discuss recent advances in PHF modeling. Microsc. Res. Tech. 67:126–140, 2005.Keywords
This publication has 89 references indexed in Scilit:
- Self-Propagating, Molecular-Level Polymorphism in Alzheimer's ß-Amyloid FibrilsScience, 2005
- Mixtures of Wild-type and a Pathogenic (E22G) Form of Aβ40 in Vitro Accumulate Protofibrils, Including Amyloid PoresJournal of Molecular Biology, 2003
- α-Synuclein, Especially the Parkinson's Disease-associated Mutants, Forms Pore-like Annular and Tubular ProtofibrilsJournal of Molecular Biology, 2002
- Transthyretin fibrillogenesis entails the assembly of monomers: a molecular model for in vitro assembled transthyretin amyloid-like fibrils 1 1Edited by M. MoodyJournal of Molecular Biology, 2002
- Structure, Microtubule Interactions, and Paired Helical Filament Aggregation by Tau Mutants of Frontotemporal DementiasBiochemistry, 2000
- RNA stimulates aggregation of microtubule‐associated protein tau into Alzheimer‐like paired helical filamentsFEBS Letters, 1996
- Differential sensitivity to proteolysis by brain calpain of adult human tau, fetal human tau and PHF‐tauFEBS Letters, 1995
- Assembly of Alzheimer‐like filaments from full‐length tau proteinFEBS Letters, 1994
- Neuropathological stageing of Alzheimer-related changesActa Neuropathologica, 1991
- Alzheimer's disease: Initial report of the purification and characterization of a novel cerebrovascular amyloid proteinBiochemical and Biophysical Research Communications, 1984