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基于 TMT 的牛肝蛋白质组学分析凸显了合成代谢处理的蛋白质标志物。

TMT-Based Proteomics Profiling of Bovine Liver Underscores Protein Markers of Anabolic Treatments.

机构信息

Department of Chemistry, Istituto Zooprofilattico Sperimentale delle Venezie, 35020, Legnaro PD, Italy.

Department of Food Safety, Istituto Zooprofilattico Sperimentale delle Venezie, 35020, Legnaro PD, Italy.

出版信息

Proteomics. 2019 May;19(9):e1800422. doi: 10.1002/pmic.201800422. Epub 2019 Apr 18.

Abstract

Illegal use of growth promoter compounds in food production exposes consumers to health risk. Surveillance of such practices is based on direct detection of drugs or related metabolites by HPLC-MS/MS. Screening strategies focusing on indirect biological responses are considered promising tools to improve surveillance. In this study, an untargeted shotgun proteomics approach based on tandem mass tags (TMTs) is carried out to identify proteins altered in bovine liver after different anabolic treatments. Three controlled pharmacological treatments with dexamethasone, a combination of dexamethasone and clenbuterol, or a combination of sexual steroids (trenbolone and estradiol) are analyzed. Untargeted TMT analysis of liver digests by high resolution MS allowed for the relative quantification of proteins. Thanks to partial least squarediscriminant analysis, a set of proteins capable to classify animals treated with dexamethasone alone (11 proteins), or in combination with clenbuterol (13 proteins) are identified. No significant difference is found upon administration of sexual steroids. After relative quantification of candidate markers by parallel reaction monitoring (PRM), two predictive models are trained to validate protein markers. Finally, an independent animal set of control bulls and bulls treated with dexamethasone is analyzed by PRM to further validate a predictive model giving an accuracy of 100%.

摘要

在食品生产中非法使用生长促进剂会使消费者面临健康风险。此类做法的监测基于 HPLC-MS/MS 对药物或相关代谢物的直接检测。侧重于间接生物反应的筛选策略被认为是改进监测的有前途的工具。在这项研究中,采用基于串联质量标签(TMT)的非靶向 shotgun 蛋白质组学方法,鉴定牛肝在不同合成代谢处理后的变化蛋白。分析了三种受控药理学处理,即地塞米松、地塞米松和克伦特罗的组合或性类固醇(群勃龙和雌二醇)的组合。通过高分辨率 MS 对肝消化物进行非靶向 TMT 分析,可进行蛋白质的相对定量。通过偏最小二乘判别分析,鉴定出一组能够对单独用地塞米松(11 种蛋白)或与克伦特罗(13 种蛋白)联合治疗的动物进行分类的蛋白。给予性类固醇后没有发现显著差异。通过平行反应监测(PRM)对候选标志物进行相对定量后,训练了两个预测模型来验证蛋白质标志物。最后,通过 PRM 分析一组独立的对照公牛和用地塞米松治疗的公牛,进一步验证预测模型的准确性为 100%。

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