2019
DOI: 10.1016/j.lwt.2018.12.059
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Purification, identification, and characterization of novel angiotensin I-converting enzyme (ACE) inhibitory peptides from alcalase digested horse gram flour

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Cited by 57 publications
(41 citation statements)
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“…These structural features all significantly contributed to its relatively high ACE-inhibitory activity (72.24 µM), which was higher (p < 0.05) than that of the peptides identified from horrens protein (GSAGY, IC 50 : 706 µM) and casein (NMAINPSKENLCSTFCK, IC 50 : 129.07 µM) [38,40]. Furthermore, the Arg at the N-terminal of RWDISQPY contributed substantially to the high activity [41]. An increasing number of studies have found that, apart from molecular mass and C-terminal tripeptides, other amino acid sequences such as Nutrients 2020, 12, 653 9 of 14 the N-terminal residue, C-terminal tetrapeptide, pentapeptide, and even heptapeptide of peptides also contribute to the inhibitory activity [25,41].…”
Section: Inhibition Kinetics Of Synthetic Peptidesmentioning
confidence: 95%
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“…These structural features all significantly contributed to its relatively high ACE-inhibitory activity (72.24 µM), which was higher (p < 0.05) than that of the peptides identified from horrens protein (GSAGY, IC 50 : 706 µM) and casein (NMAINPSKENLCSTFCK, IC 50 : 129.07 µM) [38,40]. Furthermore, the Arg at the N-terminal of RWDISQPY contributed substantially to the high activity [41]. An increasing number of studies have found that, apart from molecular mass and C-terminal tripeptides, other amino acid sequences such as Nutrients 2020, 12, 653 9 of 14 the N-terminal residue, C-terminal tetrapeptide, pentapeptide, and even heptapeptide of peptides also contribute to the inhibitory activity [25,41].…”
Section: Inhibition Kinetics Of Synthetic Peptidesmentioning
confidence: 95%
“…Compared to noncompetitive and uncompetitive inhibitors, competitive peptides seem to exhibit relatively higher ACE-inhibitory activity [4]. Bhaskar et al [41] and Lin et al [28] also identified peptides TVGMTAKF, QLLLQQ and PFPGPIPN with competitive inhibition patterns. Now, it has been demonstrated that hydrogen bonds formed between the ACE active sites (S1, S1 , and S2) and peptides' C-terminal tripeptide are crucial to ACE inhibition [6].…”
Section: Inhibition Kinetics Of Synthetic Peptidesmentioning
confidence: 99%
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“…The above results further confirmed the report that the majority of ACE-inhibitory and antioxidant peptides are short sequences with 2-12 residuals, of which hydrophobic amino acids (Phe, Val, Leu, Ile, Pro, Ala, Trp, and Met) are the major ones [10,29]. Although the structural bioinformatics showed that ACE-inhibitory activity had a negative correlation with molecular mass of peptides, RGQVIYVL (946.6 Da) showed a higher activity than that of peptides identified from tilapia skin gelatin (VGLPNSR, IC 50 = 80.9 µM), horse gram protein (QLLLQQ, IC 50 = 75.0 µM), and rice bran protein (YSK, IC 50 : 76 µM) [25,30,31]. The reason may be the presence of Tyr and branch amino acids (Val and Leu) at the C-terminal of RGQVIYVL simultaneously.…”
Section: Characterization Of Pooled Peptide Fraction By Mass Spectrommentioning
confidence: 99%