REAL

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

Gera, János and Szögi, Titanilla and Bozsó, Zsolt and Fülöp, Lívia and Barrera, Exequiel E. and Paragi, Gábor (2018) Searching for improved mimetic peptides inhibitors preventing conformational transition of amyloid-β42 monomer. BIOORGANIC CHEMISTRY, 81. pp. 211-221. ISSN 0045-2068

[img] Text
1_s2.0_S004520681830573X_main_u.pdf
Restricted to Repository staff only

Download (2MB) | Request a copy

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.

Item Type: Article
Uncontrolled Keywords: Molecular docking; Molecular dynamics; Aβ aggregation; Amyloid β-peptide; Alzheimer’s disease; Mimetic peptides
Subjects: Q Science / természettudomány > QD Chemistry / kémia
SWORD Depositor: MTMT SWORD
Depositing User: MTMT SWORD
Date Deposited: 28 Sep 2018 23:56
Last Modified: 28 Sep 2018 23:56
URI: http://real.mtak.hu/id/eprint/85859

Actions (login required)

Edit Item Edit Item