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Tau Protein Assembles into Isoform- and Disulfide-dependent Polymorphic Fibrils with Distinct Structural Properties

Tauopathies are neurodegenerative diseases in which insoluble fibrillar aggregates of a microtubule-binding protein, Tau, are abnormally accumulated. Pathological Tau fibrils often exhibit structural polymorphisms that differ among phenotypically distinct tauopathies; however, a molecular mechanism...

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Detalhes bibliográficos
Main Authors: Furukawa, Yoshiaki, Kaneko, Kumi, Nukina, Nobuyuki
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Biochemistry and Molecular Biology 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3149317/
https://ncbi.nlm.nih.gov/pubmed/21659525
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M111.248963
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