YDFYPSSTKDQQS (P3) is a peptide derived from the hydrolysis of lupin protein with pepsin that may be bioavailable, since it is absorbed in Caco-2 cells. In the framework of a research aimed at identifying new hypocholesterolemic peptides from plant proteins, this work provides evidence that P3 inhibits in vitro the functionality of 3-hydroxy-3-methylglutaryl CoA reductase (HMGCoAR) and reports the characterization of the molecular mechanism through which this peptide modulates cholesterol metabolism in HepG2 cells. Specifically, through the inhibition of HMGCoAR activity, P3 improves the low density lipoprotein receptor protein levels via SREBP-1 activation, leading to a better ability of HepG2 cells to uptake extracellular low density lipoproteins with a final in vitro hypocholesterolemic effect. Practical applications: Plant proteins have many practical applications in human nutrition, since they are environmentally sustainable and provide useful health benefits mostly in the area of hypercholesterolemia prevention. The identification of novel bioavailable hypocholesterolemic peptides and the characterization of their mechanism of action may strengthen the awareness of the role of plant proteins in human health. The mechanism through which P3 exerts its hypocholesterolemic activity is distinctive in respect to other plant peptides. Hypocholesterolemic peptides from plant proteins may be included in dietary supplements.

YDFYPSSTKDQQS (P3), a peptide from lupin protein, absorbed by Caco-2 cells, modulates cholesterol metabolism in HepG2 cells via SREBP-1 activation / C. Lammi, C. Zanoni, A. Arnoldi, G. Aiello. - In: JOURNAL OF FOOD BIOCHEMISTRY. - ISSN 0145-8884. - 42:3(2018), pp. e12524.1-e12524.8. [10.1111/jfbc.12524]

YDFYPSSTKDQQS (P3), a peptide from lupin protein, absorbed by Caco-2 cells, modulates cholesterol metabolism in HepG2 cells via SREBP-1 activation

C. Lammi
Primo
;
C. Zanoni
Secondo
;
A. Arnoldi
Penultimo
;
G. Aiello
Ultimo
2018

Abstract

YDFYPSSTKDQQS (P3) is a peptide derived from the hydrolysis of lupin protein with pepsin that may be bioavailable, since it is absorbed in Caco-2 cells. In the framework of a research aimed at identifying new hypocholesterolemic peptides from plant proteins, this work provides evidence that P3 inhibits in vitro the functionality of 3-hydroxy-3-methylglutaryl CoA reductase (HMGCoAR) and reports the characterization of the molecular mechanism through which this peptide modulates cholesterol metabolism in HepG2 cells. Specifically, through the inhibition of HMGCoAR activity, P3 improves the low density lipoprotein receptor protein levels via SREBP-1 activation, leading to a better ability of HepG2 cells to uptake extracellular low density lipoproteins with a final in vitro hypocholesterolemic effect. Practical applications: Plant proteins have many practical applications in human nutrition, since they are environmentally sustainable and provide useful health benefits mostly in the area of hypercholesterolemia prevention. The identification of novel bioavailable hypocholesterolemic peptides and the characterization of their mechanism of action may strengthen the awareness of the role of plant proteins in human health. The mechanism through which P3 exerts its hypocholesterolemic activity is distinctive in respect to other plant peptides. Hypocholesterolemic peptides from plant proteins may be included in dietary supplements.
bioavailable peptide; Caco-2 cells; hypocholesterolemic peptide; low density lipoproteins; lupin protein; lupinus albus; plant protein; SREBP-1 activation; biophysics; food science; pharmacology; cell biology
Settore CHIM/10 - Chimica degli Alimenti
2018
Article (author)
File in questo prodotto:
File Dimensione Formato  
P3.pdf

accesso riservato

Tipologia: Publisher's version/PDF
Dimensione 303.7 kB
Formato Adobe PDF
303.7 kB Adobe PDF   Visualizza/Apri   Richiedi una copia
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/557085
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 16
  • ???jsp.display-item.citation.isi??? 15
social impact