Searching for improved mimetic peptides inhibitors preventing conformational transition of amyloid-β42 monomer

Abstract

A series of novel mimetic peptides were designed, synthesised and biologically evaluated as inhibitors of Aβ₄₂ aggregation. One of the synthesised peptidic compounds, termed compound 7 modulated Aβ₄₂ aggregation as demonstrated by thioflavin T fluorescence, acting also as an inhibitor of the cytotoxicity exerted by Aβ₄₂ aggregates. The early stage interaction between compound 7 and the Aβ₄₂ monomer was investigated by replica exchange molecular dynamics (REMD) simulations and docking studies. Our theoretical results revealed that compound 7 can elongate the helical conformation state of an early stage Aβ₄₂ monomer and it helps preventing the formation of β-sheet structures by interacting with key residues in the central hydrophobic cluster (CHC). This strategy where early "on-pathway" events are monitored by small molecules will help the development of new therapeutic strategies for Alzheimer's disease.

Keywords: Alzheimer’s disease; Amyloid β-peptide; Aβ aggregation; Mimetic peptides; Molecular docking; Molecular dynamics.