绿茶儿茶素可以结合和修饰ERp57/PDIA3的活性。

Biochimica et biophysica acta Pub Date : 2013-03-01
Lucie Trnková, Daniela Ricci, Caterina Grillo, Gianni Colotti, Fabio Altieri
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引用次数: 0

摘要

背景:绿茶含有丰富的多酚,主要是儿茶素(黄烷醇),绿茶在预防和治疗各种疾病方面具有显著的有益健康作用。在这项研究中,四种绿茶儿茶素对ERp57蛋白的影响,也被称为蛋白二硫异构酶异构体A3 (PDIA3),在体外模型中进行了研究。方法:采用荧光猝灭和表面等离子体共振技术研究儿茶素与ERp57的相互作用,并研究其对ERp57活性的影响。结果:观察到对没食子酸儿茶素具有较高的亲和力,其结合接近蛋白质的硫氧还蛋白样氧化还原敏感活性位点,并倾向于氧化形式。这些儿茶素对ERp57性质的影响也被研究,观察到ERp57还原酶活性的适度抑制以及ERp57 DNA结合活性的强烈抑制。结论:考虑到没食子酸儿茶素对ERp57的高亲和力及其抑制ERp57与其他大分子配体结合的能力,儿茶素与ERp57蛋白相互作用可能对真核细胞产生一些影响。一般意义:本研究为更好地理解儿茶素生物活性的分子机制和设计新的基于多酚的erp57特异性抑制剂提供了信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Green tea catechins can bind and modify ERp57/PDIA3 activity.

Background: Green tea is a rich source of polyphenols, mainly catechins (flavanols), which significantly contribute to the beneficial health effects of green tea in the prevention and treatment of various diseases. In this study the effects of four green tea catechins on protein ERp57, also known as protein disulfide isomerase isoform A3 (PDIA3), have been investigated in an in vitro model.

Methods: The interaction of catechins with ERp57 was explored by fluorescence quenching and surface plasmon resonance techniques and their effect on ERp57 activities was investigated.

Results: A higher affinity was observed for galloylated cathechins, which bind close to the thioredoxin-like redox-sensitive active sites of the protein, with a preference for the oxidized form. The effects of these catechins on ERp57 properties were also investigated and a moderate inhibition of the reductase activity of ERp57 was observed as well as a strong inhibition of ERp57 DNA binding activity.

Conclusions: Considering the high affinity of galloylated catechins for ERp57 and their capability to inhibit ERp57 binding to other macromolecular ligands, some effects of catechins interaction with this protein on eukaryotic cells may be expected.

General significance: This study provides information to better understand the molecular mechanisms underlying the biological activities of catechins and to design new polyphenol-based ERp57-specific inhibitors.

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