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首页> 外文期刊>Molecular BioSystems >Comparison of multiple protein extraction buffers for GeLC-MS/MS proteomic analysis of liver and colon formalin-fixed, paraffin-embedded tissues
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Comparison of multiple protein extraction buffers for GeLC-MS/MS proteomic analysis of liver and colon formalin-fixed, paraffin-embedded tissues

机译:用于肝和结肠福尔马林固定,石蜡包埋组织的GeLC-MS / MS蛋白质组学分析的多种蛋白质提取缓冲液的比较

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摘要

Formalin-fixed paraffin-embedded (FFPE) tissue specimens represent a potential valuable source of samples for clinical research. Since these specimens are banked in hospital archives, large cohorts of samples can be collected in short periods of time which can all be linked with a patients' clinical history. Therefore, the use of FFPE tissue in protein biomarker discovery studies gains interest. However, despite the growing number of FFPE proteome studies in the literature, there is a lack of a FFPE proteomics standard operating procedure (SOP). One of the challenging steps in the development of such a SOP is the ability to obtain an efficient and repeatabte extraction of full length FFPE proteins. In this study, the protein extraction efficiency of eight protein extraction buffers is critically compared with GeLC-MS/MS (1D gel electrophoresis followed by in-gel digestion and LC-MS/MS). The data variation caused by using these extraction buffers was investigated since the variation is a very important aspect when using FFPE tissue as a source for biomarker detection. In addition, a qualitative comparison was made between the protein extraction efficiency and repeatability for FFPE tissue and fresh frozen tissue.
机译:福尔马林固定石蜡包埋(FFPE)组织标本代表了潜在的有价值的临床研究样品来源。由于这些标本保存在医院档案中,因此可以在短时间内收集大量样本,这些样本都可以与患者的临床病史相关联。因此,在蛋白质生物标志物发现研究中使用FFPE组织引起了人们的兴趣。然而,尽管文献中对FFPE蛋白质组学的研究越来越多,但缺乏FFPE蛋白质组学标准操作程序(SOP)。开发这样的SOP的挑战性步骤之一是获得全长FFPE蛋白的有效且可重复提取的能力。在这项研究中,将八种蛋白质提取缓冲液的蛋白质提取效率与GeLC-MS / MS(一维凝胶电泳,然后进行凝胶内消化和LC-MS / MS)进行了严格比较。由于使用FFPE组织作为生物标志物检测的来源时,变化是一个非常重要的方面,因此研究了使用这些提取缓冲液引起的数据变化。另外,在FFPE组织和新鲜冷冻组织的蛋白质提取效率和重复性之间进行了定性比较。

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  • 来源
    《Molecular BioSystems 》 |2016年第2期| 553-565| 共13页
  • 作者单位

    Research Group of Functional Genomics and Proteomics, Department of Biology, University of Leuven, Zoological Institute, Naamsestraat 59, 3000 Leuven, Belgium;

    Research Group of Functional Genomics and Proteomics, Department of Biology, University of Leuven, Zoological Institute, Naamsestraat 59, 3000 Leuven, Belgium;

    Research Group of Functional Genomics and Proteomics, Department of Biology, University of Leuven, Zoological Institute, Naamsestraat 59, 3000 Leuven, Belgium;

    Centre for Translational Cell and Tissue Research, University Hospital of Leuven, Herestraat 49, 3000 Leuven, Belgium;

    Department of Gastro-Enterology, Digestive Oncology Unit, University Hospital of Leuven, Herestraat 49, 3000 Leuven, Belgium;

    Research Group of Functional Genomics and Proteomics, Department of Biology, University of Leuven, Zoological Institute, Naamsestraat 59, 3000 Leuven, Belgium;

    Research Group of Functional Genomics and Proteomics, Department of Biology, University of Leuven, Zoological Institute, Naamsestraat 59, 3000 Leuven, Belgium;

    Flemish Institute for Technological Research (VITO), Boeretang 200, 2400 Mol, Belgium,Centre for Proteomics, University of Antwerp/Flemish Institute for Technological Research (VITO), Groenenborgerlaan 171, 2020 Antwerp, Belgium;

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