Issue 81, 2015

The mechanisms of flavonoids inhibiting conformational transition of amyloid-β42 monomer: a comparative molecular dynamics simulation study

Abstract

Flavonoids can bind Aβ42 to inhibit the aggregation of Aβ42 monomer. However, the inhibitory mechanism remains unknown. Herein, comparable molecular dynamics simulations for a total of 710 ns were performed to study its mechanism. The in silico experiments revealed that flavonoids halt the conformational transition of Aβ42 monomer by inhibiting β-sheet formation; the flavonoids push the residues D23 and K28 of Aβ42 to be exposed to solvated water, destroy the salt bridge between D23 and K28, induce the conformational distribution of Aβ42 into local minimization energy conformational state, and generate U-shaped Aβ42 configurations, which have more stable helixes and fewer unstable random coils. Moreover, simulation results from the free energy landscape and binding free energy analyses suggest that biflavonoids are superior to monoflavonoids in inhibiting conformational transition of Aβ42 monomer. These findings agree with the experimental data and may help in the design of new agents that will inhibit the conformational transition of Aβ42 so as to treat Alzheimer's disease.

Graphical abstract: The mechanisms of flavonoids inhibiting conformational transition of amyloid-β42 monomer: a comparative molecular dynamics simulation study

Supplementary files

Article information

Article type
Paper
Submitted
25 jun 2015
Accepted
28 jul 2015
First published
28 jul 2015

RSC Adv., 2015,5, 66391-66402

The mechanisms of flavonoids inhibiting conformational transition of amyloid-β42 monomer: a comparative molecular dynamics simulation study

L. Wang, R. Zeng, X. Pang, Q. Gu and W. Tan, RSC Adv., 2015, 5, 66391 DOI: 10.1039/C5RA12328C

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