Department of Pathology , University of Michigan , Ann Arbor , Michigan 48109 , United States.
Department of Computational Medicine and Bioinformatics , University of Michigan , Ann Arbor , Michigan 48109 , United States.
J Proteome Res. 2019 Feb 1;18(2):715-720. doi: 10.1021/acs.jproteome.8b00728. Epub 2018 Dec 17.
Routine identification of thousands of proteins in a single LC-MS experiment has long become the norm. With these vast amounts of data, more rigorous treatment of modified forms of peptides becomes possible. "Open search", a protein database search with a large precursor ion mass tolerance window, is becoming a popular method to evaluate possible sets of post-translational and chemical modifications in samples. The extraction of statistical information about the modification from peptide search results requires additional effort and data processing, such as recalibration of masses and accurate detection of precursors in MS1 signals. Here we present a software tool, DeltaMass, which performs kernel-density-based estimation of observed mass shifts and allows for the detection of poorly resolved mass deltas. The software also maps observed mass shifts to known modifications from public databases such as UniMod and augments them with additionally generated possible chemical changes to the molecule. Its interactive graphical interface provides an effective option for the visual interrogation of the data and the identification of potentially interesting mass shifts or unusual artifacts for subsequent analysis. However, the program can also be used in fully automated command-line mode to generate mass-shift peak lists as well.
在单个 LC-MS 实验中常规鉴定数千种蛋白质早已成为惯例。有了这些海量数据,就可以更严格地处理肽的修饰形式。“开放式搜索”是一种对样品中可能存在的一系列翻译后和化学修饰进行评估的流行方法,它是一种使用较大前体离子质量容限窗口的蛋白质数据库搜索。从肽搜索结果中提取关于修饰的统计信息需要额外的工作和数据处理,例如质量重新校准和准确检测 MS1 信号中的前体。在这里,我们介绍了一个软件工具 DeltaMass,它基于核密度进行观测质量偏移的估计,并可以检测到质量偏移分辨率较差的情况。该软件还将观测到的质量偏移映射到 UniMod 等公共数据库中的已知修饰,并将其与分子上额外生成的可能化学变化相结合。其交互式图形界面为有效查询数据提供了一个选项,并可以识别潜在有趣的质量偏移或异常伪影,以供进一步分析。但是,该程序也可以在完全自动化的命令行模式下使用,以生成质量偏移峰列表。