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可可多酚提取物介导的氧化应激反应的蛋白质组学分析。

Proteomic Analysis of Response to Oxidative Stress Mediated by Cocoa Polyphenols Extract.

机构信息

Departamento de Biotecnología, Instituto de Agroquímica y Tecnología de los Alimentos (IATA), Consejo Superior de Investigaciones Científicas (CSIC), Agustín Escardino 7, Paterna, 46980 Valencia, Spain.

Departamento de Medicina Preventiva y Salud Pública, Ciencias de la Alimentación, Bromatología, Toxicología y Medicina legal, Universidad de Valencia, Vicente Andrés Estellés s/n, Burjassot, 46100 Valencia, Spain.

出版信息

Molecules. 2020 Jan 21;25(3):452. doi: 10.3390/molecules25030452.

Abstract

The present study addressed the protective effects against oxidative stress (OS) of a cocoa powder extract (CPEX) on the protein expression profile of . A proteomic analysis was performed after culture preincubation with CPEX either without stress (-OS) or under stress conditions (+OS) (5 mM of HO). LC-MS/MS identified 33 differentially expressed proteins (-OS: 14, +OS: 19) that were included By Gene Ontology analysis in biological processes: biosynthesis of amino acids, carbohydrate metabolism and reactive oxygen species metabolic process. In a gene-knockout strains study, eight proteins were identified as putative candidates for being involved in the protective mechanism of cocoa polyphenols against OS induced by HO. CPEX was able to exert its antioxidant activity in yeast mainly through the regulation of: (a) amino acids metabolism proteins by modulating the production of molecules with known antioxidant roles; (b) stress-responsive protein Yhb1, but we were unable to fully understand its down-regulation; (c) protein Prb1, which can act by clipping Histone H3 N-terminal tails that are related to cellular resistance to DNA damaging agents.

摘要

本研究探讨了可可粉提取物 (CPEX) 对 蛋白表达谱的抗氧化应激 (OS) 保护作用。在培养物用 CPEX 预孵育后进行蛋白质组学分析,无论是否存在应激 (-OS) 或在应激条件下 (+OS) (5 mM 的 HO)。LC-MS/MS 鉴定出 33 种差异表达的蛋白质 (-OS:14,+OS:19),这些蛋白质通过基因本体分析被归入生物过程:氨基酸生物合成、碳水化合物代谢和活性氧代谢过程。在基因敲除菌株研究中,有 8 种蛋白质被鉴定为可能参与可可多酚对 HO 诱导的 OS 的保护机制。CPEX 能够在酵母中发挥其抗氧化活性,主要通过以下方式调节:(a) 通过调节具有已知抗氧化作用的分子的产生来调节氨基酸代谢蛋白;(b) 应激响应蛋白 Yhb1,但我们无法完全理解其下调;(c) Prb1 蛋白可以通过剪断与细胞抵抗 DNA 损伤剂相关的组蛋白 H3 N 端尾巴来发挥作用。

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