Simulations on the dual effects of flavonoids as suppressors of Aβ42 fibrillogenesis and destabilizers of mature fibrils.

ABSTRACT: Structural studies of the aggregation inhibition of the amyloid-β peptide (Aβ) by different natural compounds are of the utmost importance due to their great potential as neuroprotective and therapeutic agents for Alzheimer's disease. We provided the simulation of molecular dynamics for two different states of Aβ42, including "monomeric aggregation-prone state (APS)" and "U-shaped pentamers of amyloidogenic protofilament intermediates" in the absence and presence of polyphenolic flavonoids (Flvs, myricetin and morin) in order to verify the possible mechanism of Flvs fibrillogenesis suppression. Data showed that Flvs directly bind into Aβ42 species in both states of "monomeric APS β-sheets" and "pentameric amyloidogenic intermediates". Binding of Flvs with amyloidogenic protofilament interm

SUBMITTER: Gargari SA 

PROVIDER: S-EPMC7538952 | biostudies-literature | 2020 Oct

REPOSITORIES: biostudies-literature