NovoExD: De novo Peptide Sequencing for ETD/ECD Spectra

被引:3
作者
Yan, Yan [1 ]
Kusalik, Anthony J. [1 ,2 ]
Wu, Fang-Xiang [1 ,3 ]
机构
[1] Univ Saskatchewan, Div Biomed Engn, Saskatoon, SK S7N 5A9, Canada
[2] Univ Saskatchewan, Dept Comp Sci, Saskatoon, SK S7N 5A9, Canada
[3] Univ Saskatchewan, Dept Mech Engn, Saskatoon, SK S7N 5A9, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
De novo peptide sequencing; ECD/ETD spectra; graph with multiple edge types; peptide tags; fragment ion charge determination; ELECTRON-TRANSFER DISSOCIATION; TANDEM MASS-SPECTROMETRY; CAPTURE DISSOCIATION; ETD; PROTEOMICS; HCD; IDENTIFICATION; DATABASE; UTILITY; MS/MS;
D O I
10.1109/TCBB.2015.2389813
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
De novo peptide sequencing using tandem mass spectrometry (MS/MS) data has become a major computational method for sequence identification in recent years. With the development of new instruments and technology, novel computational methods have emerged with enhanced performance. However, there are only a few methods focusing on ECD/ETD spectra, which mainly contain variants of c-ions and z-ions. Here, a de novo sequencing method for ECD/ETD spectra, NovoExD, is presented. NovoExD applies a new form of spectrum graph with multiple edge types (called a GMET), considers multiple peptide tags, and integrates amino acid combination (AAC) and fragment ion charge information. Its performance is compared with another successful de novo sequencing method, pNovo+, which has an option for ECD/ETD spectra. Experiments conducted on three different datasets show that the average full length peptide identification accuracy of NovoExD is as high as 88.70 percent, and that NovoExD's average accuracy is more than 20 percent greater on all datasets than that of pNovo+.
引用
收藏
页码:337 / 344
页数:8
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