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A tool to evaluate correspondence between extraction ion chromatographic peaks and peptide-spectrum matches in shotgun proteomics experiments

机译:在shot弹枪蛋白质组学实验中评估提取离子色谱峰与肽谱匹配之间对应关系的工具

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Chromatographed peptide signals form the basis of further data processing that eventually results in functional information derived from data-dependent bottom-up proteomics assays. We seek to rank LC/MS parent ions by the quality of their extracted ion chromatograms. Ranked extracted ion chromatograms act as an intuitive physical/chemical preselection filter to improve the quality of MS/MS fragment scans submitted for database search. We identify more than 4900 proteins when considering detector shifts of less than 7 ppm. High quality parent ions for which the database search yields no hits become candidates for subsequent unrestricted analysis for PTMs. Following this rational approach, we prioritize identification of more than 5000 spectrum matches from modified peptides and confirmed the presence of acetylaldehyde-modified His/Lys. We present a logical workflow that scores data-dependent selected ion chromatograms and leverage information about semianalytical LC/LC dimension prior to MS. Our method can be successfully used to identify unexpected modifications in peptides with excellent chromatography characteristics, independent of fragmentation pattern and activation methods. We illustrate analysis of ion chromatograms detected in two different modes by RF linear ion trap and electrostatic field orbitrap.
机译:色谱分离的肽信号构成了进一步数据处理的基础,该数据处理最终导致功能信息从数据依赖的自下而上的蛋白质组学测定中获得。我们试图通过提取离子色谱图的质量对LC / MS母离子进行排名。分级提取的离子色谱图可作为直观的物理/化学预选过滤器,以提高提交给数据库搜索的MS / MS碎片扫描的质量。当考虑检测器位移小于7 ppm时,我们鉴定出4900多种蛋白质。数据库搜索不会产生任何匹配的高质量母离子将成为随后对PTM进行无限制分析的候选离子。按照这种合理的方法,我们优先考虑从修饰的肽段中识别出5000多个光谱匹配项,并确认存在乙醛修饰的His / Lys。我们提出了一个逻辑工作流程,该流程对依赖于数据的所选离子色谱图进行评分,并利用有关MS之前半分析LC / LC尺寸的信息。我们的方法可以成功地用于鉴定具有出色色谱特性的多肽中意想不到的修饰,而与片段化模式和激活方法无关。我们说明了通过RF线性离子阱和静电场orbitrap在两种不同模式下检测到的离子色谱图的分析。

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