Untargeted, spectral library-free analysis of data-independent acquisition proteomics data generated using Orbitrap mass spectrometers

被引:59
作者
Tsou, Chih-Chiang [1 ]
Tsai, Chia-Feng [2 ]
Teo, Guo Ci [3 ]
Chen, Yu-Ju [2 ]
Nesvizhskii, Alexey I. [1 ,3 ]
机构
[1] Univ Michigan, Dept Computat Med & Bioinformat, Ann Arbor, MI 48109 USA
[2] Acad Sinica, Inst Chem, Taipei, Taiwan
[3] Univ Michigan, Dept Pathol, 4237 Med Sci 1, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院;
关键词
Bioinformatics; Data-independent acquisition; PEPTIDE IDENTIFICATIONS; STATISTICAL VALIDATION; PROCESSING STRATEGIES; QUANTITATIVE-ANALYSIS; TARGETED PROTEOMICS; SEARCH TOOL; PROTEINS; MS/MS; TANDEM; QUANTIFICATION;
D O I
10.1002/pmic.201500526
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We describe an improved version of the data-independent acquisition (DIA) computational analysis tool DIA-Umpire, and show that it enables highly sensitive, untargeted, and direct (spectral library-free) analysis of DIA data obtained using the Orbitrap family of mass spectrometers. DIA-Umpire v2 implements an improved feature detection algorithm with two additional filters based on the isotope pattern and fractional peptide mass analysis. The targeted re-extraction step of DIA-Umpire is updated with an improved scoring function and a more robust, semiparametric mixture modeling of the resulting scores for computing posterior probabilities of correct peptide identification in a targeted setting. Using two publicly available Q Exactive DIA datasets generated using HEK-293 cells and human liver microtissues, we demonstrate that DIA-Umpire can identify similar number of peptide ions, but with better identification reproducibility between replicates and samples, as with conventional data-dependent acquisition. We further demonstrate the utility of DIA-Umpire using a series of Orbitrap Fusion DIA experiments with HeLa cell lysates profiled using conventional data-dependent acquisition and using DIA with different isolation window widths.
引用
收藏
页码:2257 / 2271
页数:15
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