Stevens Stanley M, Prokai-Tatrai Katalin, Prokai Laszlo
Department of Molecular Biology and Immunology, University of North Texas Health Science Center, Fort Worth, Texas 76107, USA.
Mol Cell Proteomics. 2008 Dec;7(12):2442-51. doi: 10.1074/mcp.M800065-MCP200. Epub 2008 Aug 16.
The high selectivity and throughput of tandem mass spectrometry allow for rapid identification and localization of various posttranslational protein modifications from complex mixtures by shotgun approaches. Although sequence database search algorithms provide necessary support to process the potentially enormous quantity of MS/MS spectra generated from large scale tandem mass spectrometry experiments, false positive identifications of peptide modifications may exist even after implementation of stringent identification criteria. In this report, we describe factors that lead to misinterpretation of MS/MS spectra as well as common chemical and experimental artifacts that generate false positives using the proteomics-based identification of tyrosine nitration as an example. In addition to the proposed manual validation criteria, the importance of peptide synthesis and subsequent MS/MS characterization for validation of peptide nitration demonstrated by several examples from earlier publications is also presented.
串联质谱的高选择性和高通量使得通过鸟枪法能够从复杂混合物中快速鉴定和定位各种蛋白质翻译后修饰。尽管序列数据库搜索算法为处理大规模串联质谱实验产生的潜在海量MS/MS谱图提供了必要支持,但即使实施了严格的鉴定标准,肽段修饰的假阳性鉴定仍可能存在。在本报告中,我们以基于蛋白质组学的酪氨酸硝化鉴定为例,描述了导致MS/MS谱图误判的因素以及产生假阳性的常见化学和实验假象。除了提出的手动验证标准外,还通过早期出版物中的几个例子展示了肽段合成及后续MS/MS表征对肽段硝化验证的重要性。