Brosch Markus, Swamy Sajani, Hubbard Tim, Choudhary Jyoti
The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SA, United Kingdom.
Mol Cell Proteomics. 2008 May;7(5):962-70. doi: 10.1074/mcp.M700293-MCP200. Epub 2008 Jan 23.
It is a major challenge to develop effective sequence database search algorithms to translate molecular weight and fragment mass information obtained from tandem mass spectrometry into high quality peptide and protein assignments. We investigated the peptide identification performance of Mascot and X!Tandem for mass tolerance settings common for low and high accuracy mass spectrometry. We demonstrated that sensitivity and specificity of peptide identification can vary substantially for different mass tolerance settings, but this effect was more significant for Mascot. We present an adjusted Mascot threshold, which allows the user to freely select the best trade-off between sensitivity and specificity. The adjusted Mascot threshold was compared with the default Mascot and X!Tandem scoring thresholds and shown to be more sensitive at the same false discovery rates for both low and high accuracy mass spectrometry data.
开发有效的序列数据库搜索算法,将串联质谱获得的分子量和片段质量信息转化为高质量的肽段和蛋白质鉴定结果,是一项重大挑战。我们研究了Mascot和X!Tandem在低精度和高精度质谱常见质量容差设置下的肽段鉴定性能。我们证明,对于不同的质量容差设置,肽段鉴定的灵敏度和特异性可能有很大差异,但这种影响对Mascot更为显著。我们提出了一个调整后的Mascot阈值,它允许用户在灵敏度和特异性之间自由选择最佳权衡。将调整后的Mascot阈值与默认的Mascot和X!Tandem评分阈值进行比较,结果表明,在低精度和高精度质谱数据的相同错误发现率下,调整后的阈值更具灵敏度。