Department of Chemistry, Iowa State University, Ames, IA, 50011, USA.
Ames Laboratory-US DOE, Ames, IA, 50011, USA.
J Am Soc Mass Spectrom. 2017 Mar;28(3):434-442. doi: 10.1007/s13361-016-1577-8. Epub 2017 Jan 3.
High-spatial resolution mass spectrometry imaging (MSI) is crucial for the mapping of chemical distributions at the cellular and subcellular level. In this work, we improved our previous laser optical system for matrix-assisted laser desorption ionization (MALDI)-MSI, from ~9 μm practical laser spot size to a practical laser spot size of ~4 μm, thereby allowing for 5 μm resolution imaging without oversampling. This is accomplished through a combination of spatial filtering, beam expansion, and reduction of the final focal length. Most importantly, the new laser optics system allows for simple modification of the spot size solely through the interchanging of the beam expander component. Using 10×, 5×, and no beam expander, we could routinely change between ~4, ~7, and ~45 μm laser spot size, in less than 5 min. We applied this multi-resolution MALDI-MSI system to a single maize root tissue section with three different spatial resolutions of 5, 10, and 50 μm and compared the differences in imaging quality and signal sensitivity. We also demonstrated the difference in depth of focus between the optical systems with 10× and 5× beam expanders. Graphical Abstract ᅟ.
高空间分辨率质谱成像(MSI)对于在细胞和亚细胞水平上绘制化学分布图谱至关重要。在这项工作中,我们改进了之前用于基质辅助激光解吸电离(MALDI)-MSI 的激光光学系统,将实际的激光光斑尺寸从约 9μm 提高到约 4μm,从而能够在不进行过采样的情况下实现 5μm 的分辨率成像。这是通过空间滤波、光束扩展以及减小最终焦距来实现的。最重要的是,新的激光光学系统允许通过简单地更换扩束器组件来修改光斑尺寸。使用 10×、5×和无扩束器,我们可以在不到 5 分钟的时间内常规地在4、7 和~45μm 的激光光斑尺寸之间切换。我们将这种多分辨率 MALDI-MSI 系统应用于一个单根玉米根组织切片,具有 5、10 和 50μm 的三个不同空间分辨率,并比较了成像质量和信号灵敏度的差异。我们还展示了具有 10×和 5×扩束器的光学系统之间的景深差异。图摘要ᅟ。