Tonolo Federica, Fiorese Federico, Moretto Laura, Folda Alessandra, Scalcon Valeria, Grinzato Alessandro, Ferro Stefania, Arrigoni Giorgio, Bindoli Alberto, Feller Emiliano, Bellamio Marco, Marin Oriano, Rigobello Maria Pia
Department of Biomedical Sciences, University of Padova, 35131 Padova, Italy.
Institute of Neuroscience, CNR, 35131 Padova, Italy.
Antioxidants (Basel). 2020 Jan 29;9(2):117. doi: 10.3390/antiox9020117.
Due to their beneficial properties, fermented foods are considered important constituents of the human diet. They also contain bioactive peptides, health-promoting compounds studied for a wide range of effects. In this work, several antioxidant peptides extracted from fermented milk proteins were investigated. First, enriched peptide fractions were purified and analysed for their antioxidant capacity in vitro and in a cellular model. Subsequently, from the most active fractions, 23 peptides were identified by mass spectrometry MS/MS), synthesized and tested. Peptides , , and were selected for their antioxidant effects on Caco-2 cells both in the protection against oxidative stress and inhibition of ROS production. To define their action mechanism, the activation of the Kelch-like ECH-associated protein 1/nuclear factor erythroid 2-related factor 2(Keap1/Nrf2) pathway was studied evaluating the translocation of Nrf2 from cytosol to nucleus. In cells treated with , and a higher amount of Nrf2 was found in the nucleus with respect to the control. In addition, the three active peptides, through the activation of Keap1/Nrf2 pathway, led to overexpression and increased activity of antioxidant enzymes. Molecular docking analysis confirmed the potential ability of , and to bind Keap1, showing their destabilizing effect on Keap1/Nrf2 interaction.
由于其有益特性,发酵食品被认为是人类饮食的重要组成部分。它们还含有生物活性肽,这些具有促进健康作用的化合物有着广泛的研究。在这项工作中,对从发酵乳蛋白中提取的几种抗氧化肽进行了研究。首先,对富集的肽组分进行纯化,并在体外和细胞模型中分析其抗氧化能力。随后,从活性最高的组分中,通过串联质谱(MS/MS)鉴定出23种肽,进行合成并测试。肽、、和因其对Caco-2细胞的抗氧化作用而被选中,包括对氧化应激的保护作用和对活性氧生成的抑制作用。为了确定其作用机制,研究了类ECH相关蛋白1/核因子红细胞2相关因子2(Keap1/Nrf2)通路的激活情况,评估了Nrf2从细胞质向细胞核的转位。在用、和处理的细胞中,相对于对照组,细胞核中发现了更多的Nrf2。此外,这三种活性肽通过激活Keap1/Nrf2通路,导致抗氧化酶的过表达和活性增加。分子对接分析证实了、和与Keap1结合的潜在能力,显示了它们对Keap1/Nrf2相互作用的破坏作用。