RESUMO
Recent studies have found that ß-amyloid (Aß) oligomers may play much more important roles than amyloid plaques in the pathogenesis of Alzheimer's disease (AD). However, due to the complexity of Aß, studying the structural basis of Aß oligomer toxicity is challenging. Here, we assessed the amphiphilic property and ß-hairpin structure of Aß monomer. The potential impacts of Aß oligomers and three sequence-modifying peptides on the enzyme activities of horseradish peroxidase (HRP) and alkaline phosphatase (ALP) were further evaluated. We demonstrated that Aß oligomer possesses the ability to alter the activity of two enzymes. Moreover, modifications on the hydrophobic region and ß-turn structure of Aß monomer significantly alter its impacts on the enzyme activities. In addition, these modifications also change the bonding modes of Aß monomers or oligomers binding to HRP, as assessed by molecular docking. All of these findings provide direct experimental evidence to reveal the critical roles of the amphiphilic property and ß-sheet structure of Aß monomer in its impacts on protein activity.
