Spears Ian, Lagdameo Gabriella, Black Alyson, Brown Dalton R, Johnson Cole C, Hahm Tae-Hun, Wang Wanyue, Creissen Alain, Glunde Kristine, Tressler Caitlin M
The Johns Hopkins University Applied Imaging Mass Spectrometry Core and Service Center; Division of Cancer Imaging Research; The Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine; Baltimore, Maryland, 21205, United States.
HTX Technologies, LLC, Chapel Hill, North Carolina, 27516, United States.
Anal Chem. 2025 Sep 9;97(35):19001-19008. doi: 10.1021/acs.analchem.5c01767. Epub 2025 Aug 26.
Matrix-assisted laser desorption/ionization (MALDI) mass spectrometry imaging (MSI) is a powerful tool for imaging lipids, proteins, -glycans, metabolites, and drugs in situ. A key step in MALDI MSI is matrix deposition, which must balance the extraction of molecules from the surface of the tissue without inducing excessive analyte delocalization. Further, MALDI MSI spatial resolution is limited by the size of the matrix crystals formed during matrix deposition. Minimizing crystal size is paramount to obtaining detailed images and refined data. Sublimation has been shown to be a reliable method of depositing matrix while minimizing crystal size. Since sublimation does not use any solvents to deposit the matrix, it is also theorized to minimize analyte delocalization. However, these same solvents are thought to aid in analyte extraction, which may limit detection by sublimation. In this study, we compared crystal size, analyte delocalization, and signal intensity differences when using a commercial automatic pneumatic sprayer and a sublimator for lipid imaging analyses. We tested three matrices: α-cyano-4-hydroxycinnamic acid (CHCA), 2,5-dihydroxyacetophenone (DHAP), and 2,5-dihydroxybenzoic acid (DHB) on mouse brain, heart, and kidney. Our results revealed that crystal size depended upon the matrix and whether the crystals formed on or off tissue. Our data also showed that only a subset of the lipid spectrum was susceptible to increased delocalization from spraying and decreased signal intensity from sublimation.
基质辅助激光解吸/电离(MALDI)质谱成像(MSI)是一种用于原位成像脂质、蛋白质、聚糖、代谢物和药物的强大工具。MALDI MSI的一个关键步骤是基质沉积,这必须在从组织表面提取分子的同时,避免引起过多的分析物离域。此外,MALDI MSI的空间分辨率受到基质沉积过程中形成的基质晶体大小的限制。最小化晶体大小对于获得详细图像和精确数据至关重要。升华已被证明是一种在最小化晶体大小的同时沉积基质的可靠方法。由于升华不使用任何溶剂来沉积基质,理论上它也能使分析物离域最小化。然而,这些溶剂被认为有助于分析物提取,这可能会限制升华检测。在本研究中,我们比较了使用商用自动气动喷雾器和升华器进行脂质成像分析时的晶体大小、分析物离域和信号强度差异。我们在小鼠脑、心脏和肾脏上测试了三种基质:α-氰基-4-羟基肉桂酸(CHCA)、2,5-二羟基苯乙酮(DHAP)和2,5-二羟基苯甲酸(DHB)。我们的结果表明,晶体大小取决于基质以及晶体是在组织上还是组织外形成。我们的数据还表明,只有一部分脂质谱容易受到喷雾导致的离域增加和升华导致的信号强度降低的影响。