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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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