Hennrique Taborda Ribas on Muck Rack

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Articles

Inhibitor-based modulation of huntingtin aggregation mechanisms mitigates fibril-induced cellular stress.

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By Greeshma Jain, Marina Trombetta-Lima, Irina Matlahov, Hennrique Taborda Ribas
| biorxiv.org
Abstract Huntington disease (HD) is a neurodegenerative disorder in which mutated fragments of the huntingtin protein (Htt) undergo misfolding and aggregation. Since misfolded and aggregated proteins can cause cellular stress and cytotoxicity, there is an interest in the development of small molecule aggregation inhibitors as potential modulators of HD pathogenesis. Here, we study how a polyphenol modulates the aggregation mechanism of huntingtin exon 1 (HttEx1) even at sub-stoichiometric ratios.
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Inhibitor-based modulation of huntingtin aggregation mechanisms reduces fibril toxicity

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By Greeshma Jain, Marina Trombetta-Lima, Irina Matlahov, Hennrique Taborda Ribas
| biorxiv.org
Abstract Huntington disease (HD) is a neurodegenerative disorder in which mutated fragments of the huntingtin protein (Htt) undergo misfolding and aggregation. Since misfolded and aggregated proteins can cause cytotoxicity, there is an interest in the development of small molecule aggregation inhibitors as potential modulators of HD pathogenesis. Here, we study how a polyphenol modulates the aggregation mechanism of huntingtin exon 1 (HttEx1) even at sub-stoichiometric ratios.
Open in Who Shared Issue with article?

Inhibitor-based modulation of huntingtin aggregation reduces fibril toxicity

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By Marina Trombetta-Lima, Greeshma Jain, Irina Matlahov, Hennrique Taborda Ribas
| biorxiv.org
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