Generation of Native, Untagged Huntingtin Exon1 Monomer and Fibrils Using a SUMO Fusion Strategy

Huntington's Disease (HD) is an inherited fatal neurodegenerative disease caused by a CAG expansion (≥36) in the first exon of the HD gene, resulting in the expression of the Huntingtin protein (Htt) or N-terminal fragments thereof with an expanded polyglutamine (polyQ) stretch. The exon1 of th...

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Detalles Bibliográficos
Autores principales: Reif, Andreas, Chiki, Anass, Ricci, Jonathan, Lashuel, Hilal A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MyJove Corporation 2018
Materias:
This Month in JoVE
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6102005/
https://www.ncbi.nlm.nih.gov/pubmed/30010666
http://dx.doi.org/10.3791/57506

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6102005/
https://www.ncbi.nlm.nih.gov/pubmed/30010666
http://dx.doi.org/10.3791/57506

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