Discovery of Biomarkers of a Recombinant Human Erythropoietin Administration to Thoroughbred Geldings by Label-Free Proteomics.

IF 2.6 3区 医学 Q2 BIOCHEMICAL RESEARCH METHODS
Hiu Wing Cheung, Kin-Sing Wong, Jimmy C L Tam, Adrian F Farrington, Amanda J Bond, Terence S M Wan, Emmie N M Ho
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Abstract

Erythropoiesis-stimulating agents (ESAs) continue to be a significant threat to the integrity of human and equine sports. Besides conventional direct testing, monitoring the biomarkers associated with the effects of ESAs may provide a complementary approach via indirect detection to enhance doping control. In this study, we applied label-free proteomics to discover plasma protein biomarkers in Thoroughbred geldings after administration with a long-acting form of recombinant human erythropoietin (rhEPO), methoxy polyethylene glycol epoetin beta, Mircera. Increased haematocrit, haemoglobin and red blood cell (RBC) levels were evidenced as early as 4 days post-administration in all three horses to varying extents. Tryptic peptides were obtained from plasma samples and analysed by nanoflow ultra-high-performance liquid chromatography-high-resolution tandem mass spectrometry (nano-UHPLC-HRMSMS) using data-independent acquisition. Differential protein abundance analysis has shortlisted seven protein biomarker candidates that showed significant changes specifically after Mircera administration in the treated but not in the control geldings, which comprised downregulation of two proteins, haptoglobin (HP) and haemopexin (HPX), and upregulation of five proteins, transferrin receptor 1 (TFR1), phospholipid transfer protein (PLTP), tenascin C (TNC), vascular cell adhesion molecule 1 (VCAM1) and galectin 3 binding protein (LGALS3BP). Multivariate analysis of plasma proteome has allowed the classification of control and treated samples. This is the first report on the discovery of plasma protein biomarkers of rhEPO administration to geldings. The results lay a foundation for applications of protein biomarkers for controlling the misuse of ESAs.

通过无标记蛋白质组学发现纯血马骟马使用重组人促红细胞生成素的生物标记物
促红细胞生成素(ESAs)仍然是对人类和马匹运动完整性的重大威胁。除了传统的直接检测外,监测与 ESAs 作用相关的生物标志物也是一种通过间接检测加强兴奋剂控制的补充方法。在这项研究中,我们应用无标记蛋白质组学发现了纯血马骟马在服用长效重组人促红细胞生成素(rhEPO)(甲氧基聚乙二醇环氧乙烷 beta,Mircera)后的血浆蛋白生物标记物。早在给药后 4 天,三匹马的血细胞比容、血红蛋白和红细胞(RBC)水平就出现了不同程度的升高。从血浆样本中提取了胰蛋白酶肽,并通过纳米流超高效液相色谱-高分辨串联质谱法(nano-UHPLC-HRMSMS)进行了分析,该方法采用了数据独立采集技术。差异蛋白质丰度分析筛选出了七种候选蛋白质生物标记物,这些标记物在治疗组骟马服用 Mircera 后发生了显著变化,而对照组骟马则没有,其中包括两种蛋白质的下调、转铁蛋白受体 1 (TFR1)、磷脂转移蛋白 (PLTP)、腱鞘蛋白 C (TNC)、血管细胞粘附分子 1 (VCAM1) 和半连接蛋白 3 结合蛋白 (LGALS3BP) 五种蛋白质上调。通过对血浆蛋白质组进行多变量分析,可以对对照样本和治疗样本进行分类。这是首次报道发现骟马服用 rhEPO 的血浆蛋白生物标志物。这些结果为应用蛋白质生物标志物控制ESAs的滥用奠定了基础。
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来源期刊
Drug Testing and Analysis
Drug Testing and Analysis BIOCHEMICAL RESEARCH METHODS-CHEMISTRY, ANALYTICAL
CiteScore
5.90
自引率
24.10%
发文量
191
审稿时长
2.3 months
期刊介绍: As the incidence of drugs escalates in 21st century living, their detection and analysis have become increasingly important. Sport, the workplace, crime investigation, homeland security, the pharmaceutical industry and the environment are just some of the high profile arenas in which analytical testing has provided an important investigative tool for uncovering the presence of extraneous substances. In addition to the usual publishing fare of primary research articles, case reports and letters, Drug Testing and Analysis offers a unique combination of; ‘How to’ material such as ‘Tutorials’ and ‘Reviews’, Speculative pieces (‘Commentaries’ and ‘Perspectives'', providing a broader scientific and social context to the aspects of analytical testing), ‘Annual banned substance reviews’ (delivering a critical evaluation of the methods used in the characterization of established and newly outlawed compounds). Rather than focus on the application of a single technique, Drug Testing and Analysis employs a unique multidisciplinary approach to the field of controversial compound determination. Papers discussing chromatography, mass spectrometry, immunological approaches, 1D/2D gel electrophoresis, to name just a few select methods, are welcomed where their application is related to any of the six key topics listed below.
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