Physical Electronics, Inc., Chanhassen, Minnesota 55317, United States.
Multi-Modal Molecular Imaging (M4I) Institute, Maastricht University , 6211 ER Maastricht, Netherlands.
Anal Chem. 2016 Jun 21;88(12):6433-40. doi: 10.1021/acs.analchem.6b01022. Epub 2016 May 23.
We report a method for the unambiguous identification of molecules in biological and materials specimens at high practical lateral resolution using a new TOF-SIMS parallel imaging MS/MS spectrometer. The tandem mass spectrometry imaging reported here is based on the precise monoisotopic selection of precursor ions from a TOF-SIMS secondary ion stream followed by the parallel and synchronous collection of the product ion data. Thus, our new method enables simultaneous surface screening of a complex matrix chemistry with TOF-SIMS (MS(1)) imaging and targeted identification of matrix components with MS/MS (MS(2)) imaging. This approach takes optimal advantage of all ions produced from a multicomponent sample, compared to classical tandem mass spectrometric methods that discard all ions with the exception of specific ions of interest. We have applied this approach for molecular surface analysis and molecular identification on the nanometer scale. High abundance sensitivity is achieved at low primary ion dose density; therefore, one-of-a-kind samples may be relentlessly probed before ion-beam-induced molecular damage is observed.
我们报告了一种使用新型飞行时间二次离子质谱仪平行成像 MS/MS 光谱仪在高实际横向分辨率下对生物和材料样本中的分子进行明确识别的方法。这里报道的串联质谱成像基于从飞行时间二次离子流中精确地选择单同位素前体离子,然后平行和同步收集产物离子数据。因此,我们的新方法能够同时对复杂基质化学物质进行表面筛选(MS(1)成像),并对基质成分进行靶向识别(MS/MS(MS(2))成像)。与丢弃除特定感兴趣离子之外的所有离子的传统串联质谱方法相比,这种方法可以充分利用从多组分样品中产生的所有离子。我们已经将这种方法应用于纳米尺度的分子表面分析和分子鉴定。在低初级离子剂量密度下实现了高丰度灵敏度;因此,在观察到离子束诱导的分子损伤之前,可以对独一无二的样本进行无情探测。