Investigation of the interaction of amyloid β peptide (11-42) oligomers with a 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC) membrane using molecular dynamics simulation

• Published in: Physical chemistry chemical physics : PCCP 2018, Vol.20 (10), p.6817-6829
• Main Authors: Xiang, Ning, Lyu, Yuan, Zhu, Xiao, Narsimhan, Ganesan
• Format: Article
• Language: English
• Subjects: Alzheimer's disease; Amyloid beta-Peptides - chemistry; Cell membranes; Cholesterol; Cholesterol - chemistry; Deformation mechanisms; Free energy; Humans; Hydrophobic and Hydrophilic Interactions; Lipids; Membrane Lipids - chemistry; Membranes; Membranes, Artificial; Molecular dynamics; Molecular Dynamics Simulation; Oligomers; Oligopeptides - chemistry; Parkinson's disease; Penetration; Peptide Fragments - chemistry; Peptides; Phosphatidylcholines - chemistry; Phospholipids; Pore formation; Proteins; Simulation; Thermodynamics
• ISSN: 1463-9076; 1463-9084
• DOI: 10.1039/c7cp07148e

Some amyloid related proteins/peptides are involved in aggregation and pore formation in phospholipid membranes (cell membranes), which result in a variety of neurological disorders such as Alzheimer's disease, Parkinson's disease and Huntington disease. In this research, the mechanism of pore formation by β amyloid (Aβ) peptides was investigated using molecular dynamics simulation by simulating the interaction of the Aβ(11-42) peptide, with a lipid membrane and the potential of the mean force of interaction was evaluated. A 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC) membrane system with different cholesterol concentrations was used to simulate the neural cell membrane. The results indicated that Aβ(11-42) peptide oligomers with peptide numbers larger than two were more likely to lead to lipid deformation and water channels, and the free energy of penetration into the membrane decreased with the increasing number of peptides. Increasing the concentration of cholesterol leads to a higher energy barrier for the penetration of peptide into the lipid bilayer thereby protecting the membrane. The results of this research have potential application in the prevention of pore formation by Aβ aggregates on the lipid membrane.