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Peptide Identification by Database Search of Mixture Tandem Mass Spectra

机译:通过混合串联质谱数据库搜索来鉴定肽

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摘要

In high-throughput proteomics the development of computational methods and novel experimental strategies often rely on each other. In certain areas, mass spectrom-etry methods for data acquisition are ahead of computational methods to interpret the resulting tandem mass spectra. Particularly, although there are numerous situations in which a mixture tandem mass spectrum can contain fragment ions from two or more peptides, nearly all database search tools still make the assumption that each tandem mass spectrum comes from one peptide. Common examples include mixture spectra from co-elut-ing peptides in complex samples, spectra generated from data-independent acquisition methods, and spectra from peptides with complex post-translational modifications. We propose a new database search tool (MixDB) that is able to identify mixture tandem mass spectra from more than one peptide. We show that peptides can be reliably identified with up to 95% accuracy from mixture spectra while considering only a 0.01% of all possible peptide pairs (four orders of magnitude speedup). Comparison with current database search methods indicates that our approach has better or comparable sensitivity and precision at identifying single-peptide spectra while simultaneously being able to identify 38% more peptides from mixture spectra at significantly higher precision.
机译:在高通量蛋白质组学中,计算方法的发展和新颖的实验策略经常相互依赖。在某些地区,用于数据采集的质谱方法要比用于解释所得串联质谱的计算方法领先。特别是,尽管在许多情况下混合串联质谱可能包含来自两个或多个肽段的碎片离子,但几乎所有数据库搜索工具仍假设每个串联质谱均来自一个肽。常见的例子包括复杂样品中共洗脱肽的混合光谱,从数据独立的采集方法生成的光谱以及具有复杂翻译后修饰的肽的光谱。我们提出了一种新的数据库搜索工具(MixDB),该工具能够从一个以上的肽段中识别混合串联质谱。我们显示,可以从混合物光谱中以高达95%的准确度可靠地鉴定肽,同时仅考虑所有可能的肽对中的0.01%(四个数量级的加速)。与当前数据库搜索方法的比较表明,我们的方法在鉴定单肽谱方面具有更好或相当的灵敏度和精度,同时能够以更高的精度从混合物谱中鉴定出38%的肽。

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