多肽测序的多电荷质谱建模与表征

K. F. Chong, K. Ning, H. Leong, P. Pevzner
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引用次数: 6

摘要

利用串联质谱数据对肽序列进行测序是蛋白质组学中一个重要且具有挑战性的问题。在本文中,我们解决了多电荷谱的多肽测序问题。大多数肽测序算法目前处理1或2电荷谱,并没有设计用于处理高电荷谱。通过对已有模型的推广,给出了多电荷谱的表征。利用这些新模型,我们分析了来自GPM[8]数据集的带1-5电荷的光谱。我们的分析表明,存在较高的电荷峰,它们对完整肽的预测有重要贡献。它们也有助于解释为什么现有的算法在多电荷谱上表现不佳。在此基础上提出了一种处理多电荷谱的新算法。实验结果表明,该方法在各种光谱上都表现良好,特别是在多电荷谱上。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modeling and Characterization of Multi-charge Mass Spectra for Peptide Sequencing
Sequencing of peptide sequences using tandem mass spectrometry data is an important and challenging problem in proteomics. In this paper, we address the problem of peptide sequencing for multi-charge spectra. Most peptide sequencing algorithms currently handle spectra of charge 1 or 2 and have not been designed to handle higher-charge spectra. We give a characterization of multicharge spectra by generalizing existing models. Using these new models, we have analyzed spectra with charges 1-5 from the GPM [8] datasets. Our analysis shows that higher charge peaks are present and they contribute significantly to prediction of the complete peptide. They also help to explain why existing algorithms do not perform well on multi-charge spectra. We also propose a new de novo algorithm for dealing with multi-charge spectra based on the new models. Experimental results show that it performs well on all spectra, especially so for multi-charge spectra.
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