Modern Data Acquisition Approaches in Proteomics Based on Dynamic Instrument Control

被引:4
|
作者
Plank, Michael J. [1 ,2 ]
机构
[1] Univ Arizona, Dept Mol & Cellular Biol, Tucson, AZ 85721 USA
[2] Univ Arizona, Bio5 Inst, Tucson, AZ 85721 USA
关键词
instrument control; dynamic control; intelligent data acquisition; on-the-fly; real-time decision making; retention time scheduling trigger peptides; instrument application programming interface; MASS-SPECTROMETRY; STRATEGY; ACCURATE; LIVE;
D O I
10.1021/acs.jproteome.2c00096
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Traditionally, data acquisition in mass spectrometry-based proteomics is directed by user-defined parameters and relatively simple decision making, such as selection of the highest MS1 peaks for fragmentation. In recent years, access to two-way-communication with instrument codebases has led to a surge in algorithms instructing more complex decision processes on-the-fly. A closer matching between the time windows for monitoring peptides in targeted proteomics and their actual chromatographic elution peaks has been addressed through dynamic retention time scheduling and through triggered acquisition. Strategies based on real-time database searching and spectral matching have, among others, been used to adjust acquisition parameters for selected peptides for improved quantitative accuracy. While initial studies were mainly performed on a proof-of-concept level, dynamic acquisition approaches recently became more broadly available through software and increasing integration into standard instrument control and are likely to transform the field of proteomics in the coming years.
引用
收藏
页码:1209 / 1217
页数:9
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