Tsou Chih-Chiang, Avtonomov Dmitry, Larsen Brett, Tucholska Monika, Choi Hyungwon, Gingras Anne-Claude, Nesvizhskii Alexey I
1] Department of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, Michigan, USA. [2] Department of Pathology, University of Michigan, Ann Arbor, Michigan, USA.
Department of Pathology, University of Michigan, Ann Arbor, Michigan, USA.
Nat Methods. 2015 Mar;12(3):258-64, 7 p following 264. doi: 10.1038/nmeth.3255. Epub 2015 Jan 19.
As a result of recent improvements in mass spectrometry (MS), there is increased interest in data-independent acquisition (DIA) strategies in which all peptides are systematically fragmented using wide mass-isolation windows ('multiplex fragmentation'). DIA-Umpire (http://diaumpire.sourceforge.net/), a comprehensive computational workflow and open-source software for DIA data, detects precursor and fragment chromatographic features and assembles them into pseudo-tandem MS spectra. These spectra can be identified with conventional database-searching and protein-inference tools, allowing sensitive, untargeted analysis of DIA data without the need for a spectral library. Quantification is done with both precursor- and fragment-ion intensities. Furthermore, DIA-Umpire enables targeted extraction of quantitative information based on peptides initially identified in only a subset of the samples, resulting in more consistent quantification across multiple samples. We demonstrated the performance of the method with control samples of varying complexity and publicly available glycoproteomics and affinity purification-MS data.
由于最近质谱技术(MS)的改进,人们对数据非依赖型采集(DIA)策略越来越感兴趣,在这种策略中,所有肽段都使用宽质量隔离窗口进行系统碎裂(“多重碎裂”)。DIA-Umpire(http://diaumpire.sourceforge.net/)是一个用于DIA数据的综合计算工作流程和开源软件,它能检测前体和碎片的色谱特征,并将它们组装成伪串联质谱图。这些谱图可以用传统的数据库搜索和蛋白质推断工具进行鉴定,从而实现对DIA数据的灵敏、非靶向分析,而无需光谱库。定量分析使用前体离子和碎片离子强度。此外,DIA-Umpire能够基于最初仅在一部分样品中鉴定出的肽段进行定量信息的靶向提取,从而在多个样品中实现更一致的定量。我们用不同复杂度的对照样品以及公开可用的糖蛋白质组学和亲和纯化-MS数据证明了该方法的性能。