Original paper
Molecular dissection of amyloid disaggregation by human HSP70
Abstract
The deposition of highly ordered fibrillar-type aggregates into inclusion bodies is a hallmark of neurodegenerative diseases such as Parkinson’s disease. The high stability of such amyloid fibril aggregates makes them challenging substrates for the cellular protein quality-control machinery1,2. However, the human HSP70 chaperone and its co-chaperones DNAJB1 and HSP110 can dissolve preformed fibrils of the Parkinson’s disease-linked presynaptic...
Paper Details
Title
Molecular dissection of amyloid disaggregation by human HSP70
Published Date
Nov 11, 2020
Journal
Volume
587
Issue
7834
Pages
483 - 488
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Notes
History