De novo peptide sequencing and identification with precision mass spectrometry

被引:145
作者
Frank, Ari M. [1 ]
Savitski, Mikhail M.
Nielsen, Michael L.
Zubarev, Roman A.
Pevzner, Pavel A.
机构
[1] Univ Calif San Diego, Dept Comp Sci & Engn, La Jolla, CA 92093 USA
[2] Uppsala Univ, Lab Biol & Med Mass Spect, S-75105 Uppsala, Sweden
关键词
precision MS; MS/MS; de novo; database search; pattern matching; filtration; FTMS; FT-ICR; LTQ-FT;
D O I
10.1021/pr060271u
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The recent proliferation of novel mass spectrometers such as Fourier transform, QTOF, and OrbiTrap marks a transition into the era of precision mass spectrometry, providing a 2 orders of magnitude boost to the mass resolution, as compared to low-precision ion-trap detectors. We investigate peptide de novo sequencing by precision mass spectrometry and explore some of the differences when compared to analysis of low-precision data. We demonstrate how the dramatically improved performance of de novo sequencing with precision mass spectrometry paves the way for novel approaches to peptide identification that are based on direct sequence lookups, rather than comparisons of spectra to a database. With the direct sequence lookup, it is not only possible to search a database very efficiently, but also to use the database in novel ways, such as searching for products of alternative splicing or products of fusion proteins in cancer. Our de novo sequencing software is available for download at http://peptide.ucsd.edu/.
引用
收藏
页码:114 / 123
页数:10
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