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血管紧张素转化酶(ACE)抑制肽 FPPDVA 的胃肠道消化产物的协同抑制作用研究。

Research on the Synergistic Inhibition of Angiotensin-Converting Enzyme (ACE) by the Gastrointestinal Digestion Products of the ACE Inhibitory Peptide FPPDVA.

机构信息

School of Food Sciences and Engineering, Qilu University of Technology (Shandong Academy of Sciences), Jinan, Shandong 250353, China.

School of Materials Science and Engineering, Shandong University, Jinan, Shandong 250061, China.

出版信息

J Agric Food Chem. 2024 Nov 6;72(44):24463-24475. doi: 10.1021/acs.jafc.4c05518. Epub 2024 Oct 22.

DOI:10.1021/acs.jafc.4c05518
PMID:39436688
Abstract

To gain a deeper understanding of the ACE inhibition effect, the inhibitory effect of ACE-inhibiting peptide (ACEIP) FPPDVA's digestive products on ACE was further investigated. Two novel peptides, PD (IC = 161.1 ± 1.10 μM) and DV (IC = 66.51 ± 0.99 μM) were identified in the digestive products of FPPDVA using LC-MS/MS. The Peptide Mix (FPPDVA, PD, and DV) exhibited a remarkable synergistic effect on ACE inhibition by significantly enhancing it by up to 508% compared to the individual peptides alone. Furthermore, theoretical simulations suggest that the Peptide Mix synergistically inhibits ACE activity by forming more stable complexes with the active site of ACE, facilitated by an increased number of hydrogen bonds. Additionally, Lineweaver-Burk plot analysis and spectroscopic studies further verified the presence of these stable complexes. ITC results show that the combination of Peptides Mix and ACE is a spontaneous exothermic process driven by entropy. The study showed that FPPDVA has a stronger inhibitory effect on ACE after digestion, making it suitable as an antihypertensive peptide in functional foods.

摘要

为了更深入地了解 ACE 抑制作用,进一步研究了 ACE 抑制肽(ACEIP)FPPDVA 的消化产物对 ACE 的抑制作用。通过 LC-MS/MS 鉴定出 FPPDVA 消化产物中的两种新型肽 PD(IC=161.1±1.10 μM)和 DV(IC=66.51±0.99 μM)。与单独使用肽相比,肽混合物(FPPDVA、PD 和 DV)对 ACE 抑制表现出显著的协同作用,可将 ACE 抑制活性提高多达 508%。此外,理论模拟表明,肽混合物通过与 ACE 活性位点形成更多的氢键,促进形成更稳定的复合物,从而协同抑制 ACE 活性。此外,Lineweaver-Burk 图分析和光谱研究进一步证实了这些稳定复合物的存在。ITC 结果表明,肽混合物和 ACE 的结合是一个由熵驱动的自发放热过程。研究表明,FPPDVA 消化后对 ACE 的抑制作用更强,使其适合作为功能性食品中的降压肽。

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