基于itraq和无标记的蛋白质组学方法研究人类腺病毒感染。

International journal of proteomics Pub Date : 2013-01-01 Epub Date: 2013-03-11 DOI:10.1155/2013/581862
Hung V Trinh, Jonas Grossmann, Peter Gehrig, Bernd Roschitzki, Ralph Schlapbach, Urs F Greber, Silvio Hemmi
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引用次数: 66

摘要

相对和绝对定量等压标记(iTRAQ)和无标记方法是定量蛋白质组学中广泛使用的方法。在这里,我们基于来自生物样本的大型数据集对这些蛋白质组学方法进行了详细的评估。使用未感染的人肺上皮A549细胞和感染3型或5型人腺病毒24小时的细胞的蛋白裂解液样品,比较基于itraq标记和无标记的定量。采用基于itraq标记或无标记的方法,并采用液相色谱(LC)和串联质谱(MS/MS)对所得样品进行分析。为了减少定量软件可能产生的偏差,我们在每个程序中应用了几个软件包。itraq标记的样品采用ProteinPilot和Scaffold Q+软件,无标记分析采用Progenesis LC-MS和progenisf - t2pq /T3PQ软件。应用于相同数据集的两个软件包之间的R(2)相关系数相关性良好,基于itraq -label的定量在0.48 ~ 0.78之间,无label的定量在0.5 ~ 0.86之间。与itraq标记的样品相比,无标记样品的分析显示更高水平的蛋白质上调或下调。通过Western blotting进一步评估四种下调蛋白的浓度差异。这些数据表明,无标签法比iTRAQ法更准确。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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iTRAQ-Based and Label-Free Proteomics Approaches for Studies of Human Adenovirus Infections.

Both isobaric tags for relative and absolute quantitation (iTRAQ) and label-free methods are widely used for quantitative proteomics. Here, we provide a detailed evaluation of these proteomics approaches based on large datasets from biological samples. iTRAQ-label-based and label-free quantitations were compared using protein lysate samples from noninfected human lung epithelial A549 cells and from cells infected for 24 h with human adenovirus type 3 or type 5. Either iTRAQ-label-based or label-free methods were used, and the resulting samples were analyzed by liquid chromatography (LC) and tandem mass spectrometry (MS/MS). To reduce a possible bias from quantitation software, we applied several software packages for each procedure. ProteinPilot and Scaffold Q+ software were used for iTRAQ-labeled samples, while Progenesis LC-MS and ProgenesisF-T2PQ/T3PQ were employed for label-free analyses. R (2) correlation coefficients correlated well between two software packages applied to the same datasets with values between 0.48 and 0.78 for iTRAQ-label-based quantitations and 0.5 and 0.86 for label-free quantitations. Analyses of label-free samples showed higher levels of protein up- or downregulation in comparison to iTRAQ-labeled samples. The concentration differences were further evaluated by Western blotting for four downregulated proteins. These data suggested that the label-free method was more accurate than the iTRAQ method.

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