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Characterizing and alleviating ion suppression effects in atmospheric pressure matrix‐assisted laser desorption/ionization

化学 电离 解吸 离子 软激光解吸 基质辅助激光解吸电喷雾电离 激光器 大气压激光电离 基质(化学分析) 大气压力 分析化学(期刊) 基质辅助激光解吸/电离 环境化学 色谱法 光离子化 电子电离 光学 有机化学 吸附 气象学 物理
作者
Gongyu Li,Qinjingwen Cao,Yang Liu,Kellen DeLaney,Zichuan Tian,Eugene Moskovets,Lingjun Li
出处
期刊:Rapid Communications in Mass Spectrometry [Wiley]
卷期号:33 (4): 327-335 被引量:31
标识
DOI:10.1002/rcm.8358
摘要

Rationale As a powerful ambient ion source, atmospheric pressure (AP) matrix‐assisted laser desorption/ionization (MALDI) enables direct analysis at atmospheric pressure/temperature and minimal sample preparation. With the increasing usage of AP‐MALDI sources with Orbitrap instruments, systematic characterization of the extent of ion suppression effect (ISE) in AP‐MALDI‐Orbitrap mass spectrometry imaging (MSI) is desirable. Recently, a new low‐pressure MALDI platform has been introduced that reportedly provided better sensitivity. While extensive research efforts have been devoted to improving spatial resolution, fewer studies focused on the characterization and sensitivity improvement of these MALDI platforms that, coupled with high‐resolution Orbitraps, provide powerful strategy for MSI. Methods We compared the analytical performance of AP and low‐pressure (subatmospheric) MALDI sources to study the effect of pressure control in the ion source. Using a model peptide/protein mixture, we systematically evaluated the factors influencing ISE. Furthermore, the effect of laser spot size was evaluated through tissue imaging analysis of lipids and neuropeptides. The effects of ion suppression and laser spot size have also been examined by comparing the number of identified molecular species during MSI analysis. Results Several key operating parameters including source pressure, laser energy, laser repetition rate, and microscopic slide coating materials were optimized to minimize the ISE. Under the optimal conditions, the subatmospheric AP‐MALDI‐Orbitrap platform with high spatial and mass spectral resolution enabled significantly improved coverage of several lipid and neuropeptide families in the MS analysis of mouse brain tissue sections. Conclusions The new SubAP‐MALDI source coupled with an Orbitrap mass spectrometer was established as a viable platform for in situ endogenous biomolecular analysis with increased sensitivity compared with conventional AP‐MALDI sources as evidenced by the confident identification of neuropeptides from mouse brain imaging analyses. The alleviated ISE was key to substantial performance improvement due to optimized intermediate pressure conditions and better ion collection by the ion funnel.
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