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Vibrational Circular Dichroism Sheds New Light on the Competitive Effects of Crowding and ß-Synuclein on the Fibrillation Process of α-Synuclein.
Van de Vondel, Evelien; Baatsen, Pieter; Van Elzen, Roos; Lambeir, Anne-Marie; Keiderling, Timothy A; Herrebout, Wouter A; Johannessen, Christian.
Afiliación
  • Van de Vondel E; Molecular Spectroscopy Group, Department of Chemistry , University of Antwerp , 2020 Antwerp , Belgium.
  • Baatsen P; VIB & KU Leuven Center for Brain & Disease Research , 3000 Leuven , Belgium.
  • Van Elzen R; VIB & KU Leuven BioImaging Core , 9052 Ghent , Belgium.
  • Lambeir AM; Laboratory of Medical Biochemistry, Department of Pharmacy , University of Antwerp , 2610 Wilrijk , Belgium.
  • Keiderling TA; Laboratory of Medical Biochemistry, Department of Pharmacy , University of Antwerp , 2610 Wilrijk , Belgium.
  • Herrebout WA; Department of Chemistry , University of Illinois at Chicago , Chicago , Illinois 60607 , United States.
  • Johannessen C; Molecular Spectroscopy Group, Department of Chemistry , University of Antwerp , 2020 Antwerp , Belgium.
Biochemistry ; 57(41): 5989-5995, 2018 10 16.
Article en En | MEDLINE | ID: mdl-30239196
ABSTRACT
The effects of crowding, using the crowding agent Ficoll 70, and the presence of ß-synuclein on the fibrillation process of α-synuclein were studied by spectroscopic techniques, transmission electron microscopy, and thioflavin T assays. This combined approach, in which all techniques were applied to the same original sample, generated an unprecedented understanding of the effects of these modifying agents on the morphological properties of the fibrils. Separately, crowding gives rise to shorter mutually aligned fibrils, while ß-synuclein leads to branched, short fibrils. The combination of both effects leads to short, branched, mutually aligned fibrils. Moreover, it is shown that the nondestructive technique of vibrational circular dichroism is extremely sensitive to the length and the higher-order morphology of the fibrils.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Alfa-Sinucleína / Sinucleína beta / Amiloide Límite: Humans Idioma: En Revista: Biochemistry Año: 2018 Tipo del documento: Article País de afiliación: Bélgica

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Alfa-Sinucleína / Sinucleína beta / Amiloide Límite: Humans Idioma: En Revista: Biochemistry Año: 2018 Tipo del documento: Article País de afiliación: Bélgica