From the ‡Key Laboratory of Systems Biology, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Science, Chinese Academy of Sciences, Shanghai 200031, China; §Center for Quantitative Sciences, Vanderbilt University, Nashville, Tennessee 37232-6848;
From the ‡Key Laboratory of Systems Biology, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Science, Chinese Academy of Sciences, Shanghai 200031, China;
Mol Cell Proteomics. 2015 Feb;14(2):405-17. doi: 10.1074/mcp.O114.041376. Epub 2014 Nov 30.
Isobaric labeling techniques coupled with high-resolution mass spectrometry have been widely employed in proteomic workflows requiring relative quantification. For each high-resolution tandem mass spectrum (MS/MS), isobaric labeling techniques can be used not only to quantify the peptide from different samples by reporter ions, but also to identify the peptide it is derived from. Because the ions related to isobaric labeling may act as noise in database searching, the MS/MS spectrum should be preprocessed before peptide or protein identification. In this article, we demonstrate that there are a lot of high-frequency, high-abundance isobaric related ions in the MS/MS spectrum, and removing isobaric related ions combined with deisotoping and deconvolution in MS/MS preprocessing procedures significantly improves the peptide/protein identification sensitivity. The user-friendly software package TurboRaw2MGF (v2.0) has been implemented for converting raw TIC data files to mascot generic format files and can be downloaded for free from https://github.com/shengqh/RCPA.Tools/releases as part of the software suite ProteomicsTools. The data have been deposited to the ProteomeXchange with identifier PXD000994.
等压标记技术与高分辨率质谱联用,已广泛应用于需要相对定量的蛋白质组学工作流程中。对于每个高分辨率串联质谱(MS/MS),等压标记技术不仅可以通过报告离子来定量来自不同样品的肽,还可以鉴定其来源的肽。由于与等压标记相关的离子可能在数据库搜索中充当噪声,因此在肽或蛋白质鉴定之前,应预处理 MS/MS 光谱。在本文中,我们证明 MS/MS 光谱中存在大量高频、高丰度的等压相关离子,去除等压相关离子并结合 MS/MS 预处理过程中的去同位素峰和去卷积,可显著提高肽/蛋白质鉴定的灵敏度。用户友好的软件包 TurboRaw2MGF(v2.0)已被实现,用于将原始 TIC 数据文件转换为 Mascot 通用格式文件,可从 https://github.com/shengqh/RCPA.Tools/releases 免费下载,作为 ProteomicsTools 软件套件的一部分。该数据已存入 ProteomeXchange,标识符为 PXD000994。