一种贝叶斯模型平均方法定量重叠多肽在maldy - toof质谱。

International journal of proteomics Pub Date : 2011-01-01 Epub Date: 2011-05-23 DOI:10.1155/2011/928391
Qi Zhu, Adetayo Kasim, Dirk Valkenborg, Tomasz Burzykowski
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引用次数: 4

摘要

在高分辨率MALDI-TOF质谱中,肽产生多个峰,对应于分子的同位素变体。当两个肽出现在质量坐标附近时,会发生重叠,导致难以量化这些肽的相对丰度和确切质量。为了解决这个问题,需要考虑两个因素:(1)与同位素变异体丰度有关的变率(2)补充数据中所含信息所需的额外信息内容。我们提出了一个贝叶斯模型来整合先验信息。例如,对于肽的质量分布和同位素变体的丰度,存在这样的信息。我们开发的模型允许对感兴趣的参数进行正确的估计。通过控制质谱实验和仿真研究验证了建模方法的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A bayesian model averaging approach to the quantification of overlapping peptides in an maldi-tof mass spectrum.

A bayesian model averaging approach to the quantification of overlapping peptides in an maldi-tof mass spectrum.

A bayesian model averaging approach to the quantification of overlapping peptides in an maldi-tof mass spectrum.

A bayesian model averaging approach to the quantification of overlapping peptides in an maldi-tof mass spectrum.

In a high-resolution MALDI-TOF mass spectrum, a peptide produces multiple peaks, corresponding to the isotopic variants of the molecules. An overlap occurs when two peptides appear in the vicinity of the mass coordinate, resulting in the difficulty of quantifying the relative abundance and the exact masses of these peptides. To address the problem, two factors need to be considered: (1) the variability pertaining to the abundances of the isotopic variants (2) extra information content needed to supplement the information contained in data. We propose a Bayesian model for the incorporation of prior information. Such information exists, for example, for the distribution of the masses of peptides and the abundances of the isotopic variants. The model we develop allows for the correct estimation of the parameters of interest. The validity of the modeling approach is verified by a real-life case study from a controlled mass spectrometry experiment and by a simulation study.

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