Instant spectral assignment for advanced decision tree-driven mass spectrometry

被引:46
作者
Bailey, Derek J. [2 ,5 ]
Rose, Christopher M. [2 ,5 ]
McAlister, Graeme C. [2 ]
Brumbaugh, Justin [1 ,5 ]
Yu, Pengzhi [1 ]
Wenger, Craig D. [2 ]
Westphall, Michael S. [2 ,5 ]
Thomson, James A. [1 ,4 ,6 ]
Coon, Joshua J. [2 ,3 ,5 ]
机构
[1] Morgridge Inst Res, Madison, WI 53715 USA
[2] Univ Wisconsin, Dept Chem, Madison, WI 53706 USA
[3] Univ Wisconsin, Dept Biomol Chem, Madison, WI 53706 USA
[4] Univ Wisconsin, Dept Cell & Regenerat Biol, Madison, WI 53706 USA
[5] Univ Wisconsin, Genome Ctr Wisconsin, Madison, WI 53706 USA
[6] Univ Calif Santa Barbara, Dept Mol Cellular & Dev Biol, Santa Barbara, CA 93106 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
HIGH-THROUGHPUT PROTEOMICS; PHOSPHORYLATION ANALYSIS; PROTEIN IDENTIFICATION; SEQUENCE-ANALYSIS; PEPTIDE; DISSOCIATION; MODEL; QUANTIFICATION; ACQUISITION; ACTIVATION;
D O I
10.1073/pnas.1205292109
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We have developed and implemented a sequence identification algorithm (inSeq) that processes tandem mass spectra in real-time using the mass spectrometer's (MS) onboard processors. The inSeq algorithm relies on accurate mass tandem MS data for swift spectral matching with high accuracy. The instant spectral processing technology takes similar to 16 ms to execute and provides information to enable autonomous, real-time decision making by the MS system. Using inSeq and its advanced decision tree logic, we demonstrate (i) real-time prediction of peptide elution windows en masse (similar to 3 min width, 3,000 targets), (ii) significant improvement of quantitative precision and accuracy (similar to 3x boost in detected protein differences), and (iii) boosted rates of posttranslation modification site localization (90% agreement in real-time vs. offline localization rate and an approximate 25% gain in localized sites). The decision tree logic enabled by inSeq promises to circumvent problems with the conventional data-dependent acquisition paradigm and provides a direct route to streamlined and expedient targeted protein analysis.
引用
收藏
页码:8411 / 8416
页数:6
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