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Assessment of the Multifunctional Behavior of Lupin Peptide P7 and Its Metabolite Using an Integrated Strategy.

Carmen LammiGilda AielloLuca DellafioraCarlotta BollatiGiovanna BoschinGiulia RanaldiSimonetta FerruzzaYula SambuyGianni GalavernaAnna Arnoldi
Published in: Journal of agricultural and food chemistry (2020)
LTFPGSAED (P7) is a multifunctional hypocholesterolemic and hypoglycemic lupin peptide. While assessing its angiotensin-converting enzyme (ACE) inhibitory activity, it was more effective in intestinal Caco-2 cells (IC50 of 13.7 μM) than in renal HK-2 cells (IC50 of 79.6 μM). This discrepancy was explained by the metabolic transformation mediated by intestinal peptidases, which produced two main detected peptides, TFPGSAED and LTFPG. Indeed LTFPG, dynamically generated by intestinal dipeptidyl peptidase IV as well as its parent peptide P7 were linearly absorbed by mature Caco-2 cells. An in silico study demonstrated that the metabolite was a better ligand of the ACE enzyme than P7. These results are in agreement with an in vivo study, previously performed by Aluko et al., which has shown that LTFPG is an effective hypotensive peptide. Our work highlights the dynamic nature of bioactive food peptides that may be modulated by the metabolic activity of intestinal cells.
Keyphrases
  • induced apoptosis
  • angiotensin converting enzyme
  • cell cycle arrest
  • angiotensin ii
  • endoplasmic reticulum stress
  • signaling pathway
  • amino acid
  • pi k akt