posted on 2016-02-11, 00:00authored byEmma V. Yates, Georg Meisl, Tuomas P. J. Knowles, Christopher M. Dobson
We have explored amyloid formation
using poly(amino acid) model
systems in which differences in peptide secondary structure and hydrophobicity
can be introduced in a controlled manner. We show that an environmentally
sensitive fluorescent dye, dapoxyl, is able to identify β-sheet
structure and hydrophobic surfaces, structural features likely to
be related to toxicity, as a result of changes in its excitation and
emission profiles and its relative quantum yield. These results show
that dapoxyl is a multidimensional probe of the time dependence of
amyloid aggregation, which provides information about the presence
and nature of metastable aggregation intermediates that is inaccessible
to the conventional probes that rely on changes in quantum yield alone.