2022
DOI: 10.1016/j.fshw.2022.06.009
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Identification and dipeptidyl peptidase IV (DPP-IV) inhibitory activity verification of peptides from mouse lymphocytes

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Cited by 3 publications
(3 citation statements)
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“…Peptides with scores above 0.8 were considered potential ACEIPs. 40 The specific results are presented in Table 5. It is noteworthy that NILRFF obtained a significantly high PeptideRanker score of 0.93, suggesting the possibility of having a strong ACE inhibitory activity.…”
Section: Resultsmentioning
confidence: 99%
“…Peptides with scores above 0.8 were considered potential ACEIPs. 40 The specific results are presented in Table 5. It is noteworthy that NILRFF obtained a significantly high PeptideRanker score of 0.93, suggesting the possibility of having a strong ACE inhibitory activity.…”
Section: Resultsmentioning
confidence: 99%
“…For instance, four DPP-IV inhibitory peptides derived from quinoa hydrolysate with potential IC50 values (IPI: 5.25 μM; IPV: 26.15 μM; VAYPL: 42.93 μM; IPIN: 56.58 μM) have been identified as competitive inhibitors [27]. Moreover, DPP-IV competitive inhibitory peptides were also determined in napin of rapeseed (Brassica napus) hydrolysate (IPQVS) [28], camel whey protein (VPV, YPI, VPF, EPVK, LAHKPL, YPLR) [29], and mouse lymphocytes (SGVSLAALKKALAAAGYDVEK) [30]. On the other hand, peptide NY-7 was found to be a noncompetitive inhibitor of DPP-IV, as its Km value remained stable in both situations, whether NY-7 was present or absent (Supplementary data Table S1 and Figure 4D).…”
Section: Peptide Inhibition Patterns Of Ace and Dpp-ivmentioning
confidence: 99%
“…It suggests that NY-7 has been interacted with DPP-IV receptor via the second binding sites instead of directly binding with the active sites. Until now, the DPP-IV noncompetitive inhibitors were widely common, such as peptides obtained from αlactalbumin-rich whey hydrolysate (LDQWLCEKL, IC50: 131 µM) [31], Atlantic salmon skin hydrolysate (VLATSGPG, IC50: 1.73 mM) [32], and mouse lymphocytes (SAPRHGSLGFLPRK, IC50: 23.443 mg/L) [30]. These findings clarify the inhibitory mechanisms of LY-5 and NY-7 against DPP-IV, demonstrating their potential as therapeutic agents for diseases such as diabetes.…”
Section: Peptide Inhibition Patterns Of Ace and Dpp-ivmentioning
confidence: 99%