Department of Chemistry, University of Reading, Whiteknights, Reading, RG6 6AD, UK.
Waters Corporation, Stamford Avenue, Wilmslow, SK9 4AX, UK.
Rapid Commun Mass Spectrom. 2021 Jan;35 Suppl 1(Suppl 1):e8246. doi: 10.1002/rcm.8246. Epub 2018 Sep 12.
Liquid atmospheric pressure matrix-assisted laser desorption/ionisation (AP-MALDI) has been shown to enable the production of electrospray ionisation (ESI)-like multiply charged analyte ions with little sample consumption and long-lasting, robust ion yield for sensitive analysis by mass spectrometry (MS). Previous reports have focused on positive ion production. Here, we report an initial optimisation of liquid AP-MALDI for ESI-like negative ion production and its application to the analysis of peptides/proteins, DNA and lipids.
The instrumentation employed for this study is identical to that of earlier liquid AP-MALDI MS studies for positive analyte ion production with a simple non-commercial AP ion source that is attached to a Waters Synapt G2-Si mass spectrometer and incorporates a heated ion transfer tube. The preparation of liquid MALDI matrices is similar to positive ion mode analysis but has been adjusted for negative ion mode by changing the chromophore to 3-aminoquinoline and 9-aminoacridine for further improvements.
For DNA, liquid AP-MALDI MS analysis benefited from switching to 9-aminoacridine-based MALDI samples and the negative ion mode, increasing the number of charges by up to a factor of 2 and the analyte ion signal intensities by more than 10-fold compared with the positive ion mode. The limit of detection was recorded at around 10 fmol for ATGCAT. For lipids, negative ion mode analysis provided a fully orthogonal set of detected lipids.
Negative ion mode is a sensitive alternative to positive ion mode in liquid AP-MALDI MS analysis. In particular, the analysis of lipids and DNA benefited from the complementarity of the detected lipid species and the vastly greater DNA ion signal intensities in negative ion mode.
液体常压基质辅助激光解吸/电离 (AP-MALDI) 已被证明能够在很少的样品消耗和持久、稳健的离子产率下产生电喷雾电离 (ESI) 样的多电荷分析物离子,从而实现质谱 (MS) 的灵敏分析。以前的报告集中在正离子的产生上。在这里,我们报告了液体 AP-MALDI 最初用于 ESI 样负离子产生的优化及其在肽/蛋白质、DNA 和脂质分析中的应用。
本研究中使用的仪器与早期用于正分析物离子产生的液体 AP-MALDI MS 研究相同,具有一个简单的非商业 AP 离子源,该离子源连接到 Waters Synapt G2-Si 质谱仪,并采用了加热的离子传输管。液体 MALDI 基质的制备与正离子模式分析相似,但通过将发色团更改为 3-氨基喹啉和 9-氨基吖啶,调整为负离子模式,以进一步改进,从而实现了负离子模式的分析。
对于 DNA,液体 AP-MALDI MS 分析通过切换到基于 9-氨基吖啶的 MALDI 样品和负离子模式而受益,与正离子模式相比,电荷数增加了高达 2 倍,分析物离子信号强度增加了 10 多倍。对于 ATGCAT,检测限约为 10 fmol。对于脂质,负离子模式分析提供了一组完全正交的检测脂质。
负离子模式是液体 AP-MALDI MS 分析中一种灵敏的正离子模式替代方法。特别是,脂质和 DNA 的分析受益于检测到的脂质种类的互补性以及负离子模式下 DNA 离子信号强度的大大增加。