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在 L6 肌管中具有改善的葡萄糖摄取活性的 VPP 和 IPP 的肽类似物可从谷物蛋白中释放出来。

Peptide Analogues of VPP and IPP with Improved Glucose Uptake Activity in L6 Myotubes can be Released from Cereal Proteins.

机构信息

Zhejiang Key Laboratory for Agro-Food Processing, College of Biosystems Engineering and Food Science, Zhejiang University, 866 Yuhangtang Road, Hangzhou 310058, China.

College of Animal Sciences, Zhejiang University, Hangzhou 310058, China.

出版信息

J Agric Food Chem. 2021 Mar 10;69(9):2875-2883. doi: 10.1021/acs.jafc.1c00587. Epub 2021 Mar 1.

Abstract

VPP (Val-Pro-Pro) and IPP (Ile-Pro-Pro) are two famous antihypertensive peptides with possible benefits for type 2 diabetes mellitus (T2DM). The study was aimed to investigate the effect of peptide analogues of VPP and IPP on glucose uptake activity in L6 myotubes. The analogues were designed by replacing the N-terminal, middle, or C-terminal amino acid residues of VPP and IPP with one amino acid at a time from five amino acid groups (polar, nonpolar, basic, acidic, and aromatic amino acids). Among 26 tripeptides tested, IQP, IPQ, VPE, and VEP showed significantly higher glucose uptake activity than their parent peptides, and all were successfully released from rice proteins at the contents of 5415.82 ± 63.34, 1586.77 ± 14.94, 354.07 ± 6.56, and 596.10 ± 2.32 ng/mg dry basis, respectively, and quantified by liquid chromatography-mass spectrometry (MS)/MS using multiple reaction monitoring. All four peptides were shown to promote glucose uptake the adenosine monophosphate-activated protein kinase pathway accompanied by glucose transporter type 4 (Glut4) translocation rather than the insulin signaling pathway.

摘要

VPP(缬氨酰-脯氨酰-脯氨酸)和 IPP(异亮氨酰-脯氨酰-脯氨酸)是两种著名的具有降血压作用的肽,可能对 2 型糖尿病(T2DM)有益。本研究旨在研究 VPP 和 IPP 肽类似物对 L6 肌管葡萄糖摄取活性的影响。通过一次用来自 5 种氨基酸(极性、非极性、碱性、酸性和芳香族氨基酸)的 1 种氨基酸替换 VPP 和 IPP 的 N 端、中间或 C 端氨基酸残基来设计类似物。在测试的 26 种三肽中,IQP、IPQ、VPE 和 VEP 显示出比其母体肽更高的葡萄糖摄取活性,并且在 5415.82±63.34、1586.77±14.94、354.07±6.56 和 596.10±2.32ng/mg 干基的含量下,均能成功从大米蛋白中释放出来,通过液相色谱-质谱(MS)/MS 进行多重反应监测定量分析。这四种肽都被证明能通过 AMPK 途径促进葡萄糖摄取,同时伴有 Glut4 转位,而不是胰岛素信号通路。

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