碎片(计算)
质谱法
毫秒
离子
化学
离子迁移光谱法
分析化学(期刊)
四极
离子阱
四极飞行时间
灵敏度(控制系统)
洗脱
色谱法
串联质谱法
物理
原子物理学
计算机科学
操作系统
工程类
有机化学
电子工程
天文
作者
Florian Meier,Scarlet Beck,Niklas Graßl,Markus Lubeck,Melvin A. Park,Oliver Raether,Matthias Mann
标识
DOI:10.1021/acs.jproteome.5b00932
摘要
In liquid chromatography-mass spectrometry (LC-MS)-based proteomics, many precursors elute from the column simultaneously. In data-dependent analyses, these precursors are fragmented one at a time, whereas the others are discarded entirely. Here we employ trapped ion mobility spectrometry (TIMS) on an orthogonal quadrupole time-of-flight (QTOF) mass spectrometer to remove this limitation. In TIMS, all precursor ions are accumulated in parallel and released sequentially as a function of their ion mobility. Instead of selecting a single precursor mass with the quadrupole mass filter, we here implement synchronized scans in which the quadrupole is mass positioned with sub-millisecond switching times at the m/z values of appropriate precursors, such as those derived from a topN precursor list. We demonstrate serial selection and fragmentation of multiple precursors in single 50 ms TIMS scans. Parallel accumulation–serial fragmentation (PASEF) enables hundreds of MS/MS events per second at full sensitivity. Modeling the effect of such synchronized scans for shotgun proteomics, we estimate that about a 10-fold gain in sequencing speed should be achievable by PASEF without a decrease in sensitivity.
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