Lee Sunyoung, Li Zhiyu, Valentine Stephen J, Zucker Steven M, Webber Nathaniel, Reilly James P, Clemmer David E
Department of Chemistry, Indiana University, Bloomington, IN 47405.
Int J Mass Spectrom. 2012 Jan 1;309:154-160. doi: 10.1016/j.ijms.2011.09.011.
A new method is presented for constructing ion mobility distributions of precursor ions based upon the extraction of drift time distributions that are monitored for selected fragment ions. The approach is demonstrated with a recently designed instrument that combines ion mobility spectrometry (IMS) with ion trap mass spectrometry (MS) and ion fragmentation, as shown in a recent publication [J. Am. Soc. Mass Spectrom. 22 (2011) 1477-1485]. Here, we illustrate the method by examining selected charge states of electrosprayed ubiquitin ions, an extract from diesel fuel, and a mixture of phosphorylated peptide isomers. For ubiquitin ions, extraction of all drift times over small mass-to-charge (m/z) ranges corresponding to unique fragments of a given charge state allows the determination of precursor ion mobility distributions. A second example of the utility of the approach includes the distinguishing of precursor ion mobility distributions for isobaric, basic components from commercially available diesel fuel. Extraction of data for a single fragment ion is sufficient to distinguish the precursor ion mobility distribution of cycloalkyl-pyridine derivatives from pyrindan derivatives. Finally, the method is applied for the analysis of phosphopeptide isomers (LFpTGHPESLER and LFTGHPEpSLER) in a mixture. The approach alleviates several analytical challenges that include separation and characterization of species having similar (or identical) m/z values within complex mixtures.
本文提出了一种新方法,用于基于对选定碎片离子监测的漂移时间分布的提取来构建前体离子的离子迁移率分布。该方法已通过最近设计的一种仪器得到验证,该仪器将离子迁移谱(IMS)与离子阱质谱(MS)及离子碎裂相结合,如最近一篇出版物所示[《美国质谱学会杂志》22(2011)1477 - 1485]。在此,我们通过研究电喷雾泛素离子的选定电荷态、柴油提取物以及磷酸化肽异构体混合物来说明该方法。对于泛素离子,在对应于给定电荷态独特碎片的小质荷比(m/z)范围内提取所有漂移时间,可确定前体离子迁移率分布。该方法实用性的第二个例子包括区分市售柴油中同量异位、碱性成分的前体离子迁移率分布。提取单个碎片离子的数据足以区分环烷基吡啶衍生物与吡吲哚衍生物的前体离子迁移率分布。最后,该方法应用于混合物中磷酸化肽异构体(LFpTGHPESLER和LFTGHPEpSLER)的分析。该方法缓解了几个分析难题,包括在复杂混合物中分离和表征具有相似(或相同)m/z值的物种。