Fibril polymorphism affects immobilized non-amyloid flanking domains of huntingtin exon1 rather than its polyglutamine core
Hsiang-Kai Lin, Jennifer C. Boatz, Inge E. Krabbendam and 6 more
Nature Communications · 2017
doi:10.1038/ncomms15462 (opens in a new tab)
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Abstract
Huntington's disease is caused by a polyglutamine stretch expansion in the first exon of huntingtin. Here, the authors use infrared spectroscopy and solid-state NMR and show that polymorphic huntingtin exon1 fibres differ in their flanking regions but not their core polyglutamine amyloid structures.
Abstract licence: CC BY-NC-ND
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