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Detection of amyloid-beta fibrils using the DNA-intercalating dye YOYO-1: Binding mode and fibril formation kinetics

David Lindberg (Institutionen för biologi och bioteknik, Kemisk biologi) ; Elin Esbjörner (Institutionen för biologi och bioteknik, Kemisk biologi)
Biochemical and Biophysical Research Communications (0006-291X). Vol. 469 (2016), 2, p. 313-318.
[Artikel, refereegranskad vetenskaplig]

Identification of the chemical and biological properties of amyloid fibrils is important for understanding their roles in human diseases and to clarify the mechanisms that govern their formation. In pursuit of these goals, small molecule fluorescent dyes have received increasing attention as probes of amyloid conformations. In this study, we report on the ability of YOYO-1, a homodimeric derivative of oxazole yellow, to detect fibrils formed by the Alzheimer's disease related A beta(1-42) peptide. We find that YOYO-1 binds to A beta(1-42) fibrils with the long axes of its oxazole yellow moieties parallel to the fibril axis, resulting in a 200x emission enhancement; a result that shows that YOYO-1 is a sensitive amyloid probe. Further, YOYO-1 exhibits characteristic absorption shifts upon binding to the A beta(1-42) fibrils that we attribute to a self-stacking to non-stacking transition in its homodimer configuration; herein we show how this phenomenon can be exploited to estimate the degree of dye binding. Furthermore, we show that YOYO-1 can be used to monitor the kinetics of amyloid formation reactions. Taken together, our results show that YOYO-1 is a sensitive amyloid probe that can operate with both absorption and fluorescence read-outs, and this suggests that this commercially available dye could become a useful complement to thioflavin-T for in vitro amyloid-sensing applications.

Nyckelord: YOYO-1, Thioflavin-T, Amyloid fibril, Amyloid-beta, Fluorescence, Linear dichroism

Denna post skapades 2016-02-17.
CPL Pubid: 232146


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Institutioner (Chalmers)

Institutionen för biologi och bioteknik, Kemisk biologi


Biokemi och molekylärbiologi

Chalmers infrastruktur

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