Literature DB >> 16104001

Characterization of paired helical filaments by scanning transmission electron microscopy.

Hanna Ksiezak-Reding1, Joseph S Wall.   

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.

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Year:  2005        PMID: 16104001     DOI: 10.1002/jemt.20188

Source DB:  PubMed          Journal:  Microsc Res Tech        ISSN: 1059-910X            Impact factor:   2.769


  17 in total

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Authors:  Claire Goldsbury; Ulrich Baxa; Martha N Simon; Alasdair C Steven; Andreas Engel; Joseph S Wall; Ueli Aebi; Shirley A Müller
Journal:  J Struct Biol       Date:  2010-09-22       Impact factor: 2.867

2.  Characterization of tau fibrillization in vitro.

Authors:  Shaohua Xu; Kurt R Brunden; John Q Trojanowski; Virginia M-Y Lee
Journal:  Alzheimers Dement       Date:  2010-03       Impact factor: 21.566

3.  Nucleation-dependent tau filament formation: the importance of dimerization and an estimation of elementary rate constants.

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Journal:  J Biol Chem       Date:  2008-03-21       Impact factor: 5.157

Review 4.  Modulation and detection of tau aggregation with small-molecule ligands.

Authors:  Edward Chang; Nicolette S Honson; Bhaswati Bandyopadhyay; Kristen E Funk; Jordan R Jensen; Sohee Kim; Swati Naphade; Jeff Kuret
Journal:  Curr Alzheimer Res       Date:  2009-10       Impact factor: 3.498

Review 5.  Amyloidogenesis of Tau protein.

Authors:  Bartosz Nizynski; Wojciech Dzwolak; Krzysztof Nieznanski
Journal:  Protein Sci       Date:  2017-09-13       Impact factor: 6.725

6.  Tau protein assembles into isoform- and disulfide-dependent polymorphic fibrils with distinct structural properties.

Authors:  Yoshiaki Furukawa; Kumi Kaneko; Nobuyuki Nukina
Journal:  J Biol Chem       Date:  2011-06-09       Impact factor: 5.157

7.  Secondary nucleating sequences affect kinetics and thermodynamics of tau aggregation.

Authors:  Christopher L Moore; Michael H Huang; Shauna A Robbennolt; Kellen R Voss; Benjamin Combs; T Chris Gamblin; Warren J Goux
Journal:  Biochemistry       Date:  2011-11-29       Impact factor: 3.162

Review 8.  Evidence that non-fibrillar tau causes pathology linked to neurodegeneration and behavioral impairments.

Authors:  Kurt R Brunden; John Q Trojanowski; Virginia M-Y Lee
Journal:  J Alzheimers Dis       Date:  2008-08       Impact factor: 4.472

Review 9.  Tau aggregation and toxicity in tauopathic neurodegenerative diseases.

Authors:  Nicolette S Honson; Jeff Kuret
Journal:  J Alzheimers Dis       Date:  2008-08       Impact factor: 4.472

10.  Polymer-Peptide Conjugates Convert Amyloid into Protein Nanobundles through Fragmentation and Lateral Association.

Authors:  John W Smith; Xing Jiang; Hyosung An; Alexander M Barclay; Giuseppe Licari; Emad Tajkhorshid; Edwin G Moore; Chad M Rienstra; Jeffrey S Moore; Qian Chen
Journal:  ACS Appl Nano Mater       Date:  2019-09-10
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