A Molecular Integrative Study on the Inhibitory Effects of WRR and ERW on Amyloid β Peptide (1–42) Polymerization and Cell Toxicity

• Published in: Polymers 2023-11, Vol.15 (22), p.4356
• Main Authors: Wu, Zhongyun, Ye, Lianmeng, Yuan, Nan, Che Ajuyo, Nuela Manka’a, Xiao, Zhengpan, Liu, Liangwang, Chen, Zuqian, Pei, Yechun, Min, Yi, Wang, Dayong
• Format: Article
• Language: English
• Subjects: Amino acids; Analysis; Antibiotics; Apoptosis; Cell culture; Electron microscopes; Energy; Enzymes; Flow cytometry; Free energy; Hydrogen bonds; Identification and classification; Methods; Microscopy; Molecular docking; Molecular dynamics; Oligopeptides; Open source software; Peptides; Polymerization; Properties; Proteins; Structure; Toxic diseases; Toxicity
• ISSN: 2073-4360; 2073-4360
• DOI: 10.3390/polym15224356

Alzheimer’s disease (AD) is a neurodegenerative disease and the main pathological characteristic of AD is the deposition of Aβ42 in the brain. Inhibition of Aβ42 polymerization is one of the important research directions. Due to the pathological complexity of Alzheimer’s disease, studies on Aβ42 polymerization inhibitors have not made significant progress worldwide. Using an independently constructed structure database of oligopeptides, in this study, molecular docking, umbrella sampling analysis of free energy, ThT fluorescence detection of Aβ42 polymerization, transmission electron microscopy, and flow cytometry detection of reactive oxygen species (ROS) and apoptosis were performed to screen tripeptides and pentapeptides that inhibit polymerization. It was found that two tripeptides, i.e., WRR and ERW, bind stably to the core of Aβ42 polymerization in the molecular dynamics analysis, and they significantly inhibited the aggregation of Aβ42 and reduced their cell toxicity in vitro.