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Refining comparative proteomics by spectral counting to account for shared peptides and multiple search engines

机译:通过光谱计数细化比较蛋白质组学以考虑共享肽和多个搜索引擎

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摘要

Spectral counting has become a widely used approach for measuring and comparing protein abundance in label-free shotgun proteomics. However, when analyzing complex samples, the ambiguity of matching between peptides and proteins greatly affects the assessment of peptide and protein inventories, differentiation, and quantification. Meanwhile, the configuration of database searching algorithms that assign peptides to MS/MS spectra may produce different results in comparative proteomic analysis. Here, we present three strategies to improve comparative proteomics through spectral counting. We show that comparing spectral counts for peptide groups rather than for protein groups forestalls problems introduced by shared peptides. We demonstrate the advantage and flexibility of this new method in two datasets. We present four models to combine four popular search engines that lead to significant gains in spectral counting differentiation. Among these models, we demonstrate a powerful vote counting model that scales well for multiple search engines. We also show that semi-tryptic searching outperforms tryptic searching for comparative proteomics. Overall, these techniques considerably improve protein differentiation on the basis of spectral count tables.
机译:光谱计数已成为测量和比较无标记shot弹枪蛋白质组学中蛋白质丰度的一种广泛使用的方法。但是,当分析复杂样品时,肽段和蛋白质之间匹配的歧义性会极大地影响肽段和蛋白质清单的评估,区分和定量。同时,将肽分配给MS / MS光谱的数据库搜索算法的配置在比较蛋白质组学分析中可能会产生不同的结果。在这里,我们提出了三种通过光谱计数来改善比较蛋白质组学的策略。我们显示,比较肽组而不是蛋白质组的光谱计数可以防止共享肽引入的问题。我们在两个数据集中展示了这种新方法的优势和灵活性。我们提出了四个模型,以结合四个流行的搜索引擎,这些搜索引擎可显着提高频谱计数差异。在这些模型中,我们演示了一个强大的投票计数模型,该模型可以很好地适用于多个搜索引擎。我们还表明,半胰蛋白酶搜索优于胰蛋白酶搜索的比较蛋白质组学。总体而言,这些技术可在光谱计数表的基础上极大地改善蛋白质的分化。

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