Novel ACE inhibitory tripeptides from ovotransferrin using bioinformatics and peptidomics approaches

Sci Rep. 2019 Nov 22;9(1):17434. doi: 10.1038/s41598-019-53964-y.

Abstract

Food-derived ACE inhibitory peptides have recently attracted increased attention. This work focused on a more efficient in silico method to find ACE inhibitory peptides from ovotransferrin. In this work, ovotransferrin was digested into peptides by virtual enzymolysis. Subsequently, in vitro ACE inhibitory activity of potential tripeptides was conducted following the peptide score, toxicity, and water solubility prediction. Both pharmacophore study and flexible docking were applied to analyze ACE inhibition mechanism of tripeptides. Our results demonstrated that EWL was a potent ACE inhibitory tripeptide with IC50 value of 380 ± 10 μM. Besides, pharmacophore and flexible docking showed that the pi interaction and hydrogen bond were the key interactions in ACE-EWL complex. It appears that the in vitro ACE inhibitory activity of tripeptide EWL was consistent with its molecular modeling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiotensin-Converting Enzyme Inhibitors
  • Computational Biology* / methods
  • Conalbumin* / chemistry
  • Ligands
  • Molecular Docking Simulation
  • Molecular Dynamics Simulation
  • Peptides* / chemistry
  • Protein Binding
  • Proteolysis
  • Proteome*
  • Proteomics*

Substances

  • Angiotensin-Converting Enzyme Inhibitors
  • Ligands
  • Peptides
  • Proteome
  • Conalbumin