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Robust estimation of peptide abundance ratios and rigorous scoring of their variability and bias in quantitative shotgun proteomics

机译:定量估计shot弹枪蛋白质组学中肽丰度比的严格估计及其变异性和偏差的严格评分

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The abundance ratio between the light and heavy isotopologues of an isotopically labeled peptide can be estimated from their selected ion chromatograms. However, quantitative shotgun proteomics measurements yield selected ion chromatograms at highly variable signal-to-noise ratios for tens of thousands of peptides. This challenge calls for algorithms that not only robustly estimate the abundance ratios of different peptides but also rigorously score each abundance ratio for the expected estimation bias and variability. Scoring of the abundance ratios, much like scoring of sequence assignment for tandem mass spectra by peptide identification algorithms, enables filtering of unreliable peptide quantification and use of formal statistical inference in the subsequent protein abundance ratio estimation. In this study, a parallel paired covariance algorithm is used for robust peak detection in selected ion chromatograms. A peak profile is generated for each peptide, which is a scatterplot of ion intensities measured for the two isotopologues within their chromatographic peaks. Principal component analysis of the peak profile is proposed to estimate the peptide abundance ratio and to score the estimation with the signal-to-noise ratio of the peak profile ( profile signal-to-noise ratio). We demonstrate that the profile signal-to-noise ratio is inversely correlated with the variability and bias of peptide abundance ratio estimation.
机译:同位素标记的肽的轻同位素和重同位素之间的丰度比可以根据其选择的离子色谱图估算。但是,定量shot弹枪蛋白质组学测量结果会以成千上万种肽的信噪比在高度可变的条件下生成选定的离子色谱图。这一挑战要求算法不仅要可靠地估计不同肽的丰度比,而且还要对每个丰度比进行严格的评分,以获得预期的估计偏差和可变性。丰度比的计分,与通过肽段识别算法为串联质谱进行序列分配的计分非常相似,可以过滤不可靠的肽段定量,并在随后的蛋白质丰度比估算中使用形式统计推断。在这项研究中,并行配对协方差算法用于在选定离子色谱图中进行稳健的峰检测。为每个肽生成一个峰图,这是在其色谱峰内为两个同位素分子测得的离子强度的散点图。提出了峰轮廓的主成分分析,以估计肽丰度比,并用峰轮廓的信噪比(轮廓信噪比)对估计值打分。我们证明,配置文件信噪比与肽丰度比估计的可变性和偏差成反比。

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