Anti-Alzheimers activity and molecular mechanism of albumin-derived peptides against AChE and BChE

Food Funct. 2018 Feb 21;9(2):1173-1178. doi: 10.1039/c7fo01462g.

Abstract

Alzheimer's disease (AD) is a global health issue affecting millions of elderly people worldwide. The aim of the present study was to identify novel anti-AD peptides isolated from albumin. Anti-AD activities of the peptides were evaluated via inhibitory activities on acetylcholinesterase (AChE) and butyrylcholinesterase (BChE). Furthermore, the potential molecular mechanisms of the KLPGF/AChE were investigated by CDOCKER of Discovery studio 2017. The results revealed that peptide KLPGF could effectively inhibit AChE with an inhibition rate of 61.23% at a concentration of 50 μg mL-1. In addition, the peptide KLPGF came in contact with acylation sites and peripheral anion sites of AChE. The present study demonstrates that the peptide KLPGF could become a potential functional food intervention in AD.

MeSH terms

  • Acetylcholinesterase / chemistry
  • Acetylcholinesterase / metabolism*
  • Albumins / chemistry*
  • Alzheimer Disease / drug therapy
  • Alzheimer Disease / enzymology*
  • Butyrylcholinesterase / chemistry
  • Butyrylcholinesterase / metabolism*
  • Cholinesterase Inhibitors / chemistry*
  • Humans
  • Hydrolysis
  • Molecular Docking Simulation
  • Peptides / chemistry*

Substances

  • Albumins
  • Cholinesterase Inhibitors
  • Peptides
  • Acetylcholinesterase
  • Butyrylcholinesterase