Institute of Biotechnology in Medicine, National Yang Ming University, Taipei, Taiwan, ROC.
J Proteomics. 2013 Oct 8;91:375-84. doi: 10.1016/j.jprot.2013.07.030. Epub 2013 Aug 8.
Mass measurement and precursor mass assignment are independent processes in proteomic data acquisition. Due to misassignments to C-13 peak, or for other reasons, extensive precursor mass shifts (i.e., deviations of the measured from calculated precursor neutral masses) in LC-MS/MS data obtained with the high-accuracy LTQ-Orbitrap mass spectrometers have been reported in previous studies. Although computational methods for post-acquisition reassignment to monoisotopic mass have been developed to curate the MS/MS spectra prior to database search, a simpler method for estimating the fraction of spectra with precursor mass shift so as to determine whether the data require curation remains desirable. Here, we provide the evidence that an easy approach, which applies a large precursor tolerance (2.1Da or higher) in SEQUEST search against a forward and decoy protein sequence database and then filters the data with PeptideProphet peptide identification probability (p≥0.9), could detect most of the MS/MS spectra containing inaccurate precursor masses. Furthermore, through the implementation of artificial mass shifts on 4000 randomly selected MS/MS spectra, which originally had accurate precursor mass assigned by the mass spectrometers, we demonstrated that the accuracy of the precursor mass has almost negligible influence on the efficacy and fidelity of peptide identification.
Integral precursor mass shift is a known problem and thus proteomic data should be handled and analyzed properly to avoid losing important protein identification and/or quantification information. A quick and easy approach for estimating the number of MS/MS spectra with inaccurate precursor mass assignments would be helpful for evaluating the performance of the instrument, determining whether the data requires curation prior to database search or should be searched with specific search parameter(s). Here we demonstrated most of the MS/MS spectra with inaccurate mass assignments (integral or non-integral changes) that could be easily identified by database search with large precursor tolerance windows.
在蛋白质组学数据采集过程中,质量测量和前体质量分配是两个独立的过程。由于 C-13 峰的错误分配,或由于其他原因,在使用高精度 LTQ-Orbitrap 质谱仪获得的 LC-MS/MS 数据中,已经有报道称存在广泛的前体质量偏移(即,实测前体中性质量与计算前体中性质量之间的偏差)。尽管已经开发了用于在数据库搜索之前对后获取的重新分配到单同位素质量的计算方法,但仍然需要一种更简单的方法来估计具有前体质量偏移的谱图的分数,以便确定数据是否需要进行处理。在这里,我们提供了证据表明,一种简单的方法,即在 SEQUEST 搜索中对正向和诱饵蛋白质序列数据库应用较大的前体容忍度(2.1Da 或更高),然后使用 PeptideProphet 肽鉴定概率(p≥0.9)过滤数据,可以检测到大多数包含不准确前体质量的 MS/MS 谱图。此外,通过在 4000 个随机选择的 MS/MS 谱图上实施人工质量偏移,这些谱图最初由质谱仪准确地分配了前体质量,我们证明了前体质量的准确性对肽鉴定的效果和保真度几乎没有影响。
整体前体质量偏移是一个已知的问题,因此应正确处理和分析蛋白质组学数据,以避免丢失重要的蛋白质鉴定和/或定量信息。一种快速简便的方法来估计具有不准确前体质量分配的 MS/MS 谱图的数量,将有助于评估仪器的性能,确定数据是否需要在数据库搜索之前进行处理,或者是否应该使用特定的搜索参数进行搜索。在这里,我们证明了大多数具有不准确质量分配(整体或非整体变化)的 MS/MS 谱图可以通过使用大的前体容忍窗口的数据库搜索轻松识别。