Background: Alzheimer's disease (AD) affects mainly elderly people over 60 years of age.
Currently, there are more than 35 million people with this disease worldwide. The enzyme β-secretase
is involved in the processing of the amyloid precursor protein and plays a key role in the physiopathology
of AD. The action of some acetylcholinesterase inhibitors (AChEI) as β-secretase inhibitors has
Objective: The aim of this study was to highlight the modes of the binding of acetylcholinesterase
ligands onto the active site of the β-secretase enzyme.
Methods: Molecular dynamics and docking were used in order to identify pivotal interactions that favor
the inhibitory activity and provide a rational basis for planning novel β-secretase inhibitors. Additionally,
density functional theory (DFT) was used to provide accurate energy values for the complexes.
A mechanistic study of the amide hydrolysis was also performed at the M06/6-31G(d) basis set.
Results: Of the 100 AChE inhibitors, 10 were able to interact with Asp32 and/or Asp228 residues from
the enzyme BACE-1, suggesting that these could act as multi-target compounds. These inhibitors were
selected for DFT studies in order to provide more accurate energy values. Interestingly, the range of
energy values (-27.01 to -8.64 kJ mol-1) obtained was in agreement with the anti-AChE activity. The
results obtained in the mechanistic study of compound 93 using DFT are in agreement with theoretical
studies described in the literature.
Conclusion: The results reported in this study will advance our understanding of the influence of the
distinct chemical structures of inhibitors at the active site and aid the development of new virtual
screening protocols to design novel AChE multi-target inhibitors.