Evaluation of Aß fibrillization inhibitory effect by a PEG-peptide conjugate based on an Aß peptide fragment with intramolecular FRET.

A PEG-peptide conjugate based on an amyloid ß peptide fragment was synthesized. The formed amyloid protofibril-like aggregates induced intramolecular FRET. It proved to be useful as a bioprobe to evaluate the inhibitory effect of organic molecules toward amyloid fibrillization.