Department of Chemistry and the Beckman Institute, University of Illinois, Urbana, Illinois 61801, USA.
Anal Chem. 2011 Dec 1;83(23):9181-5. doi: 10.1021/ac201857k. Epub 2011 Nov 4.
Matrix-assisted laser desorption/ionization (MALDI) mass spectrometry imaging (MSI) combines information-rich chemical detection with spatial localization of analytes. For a given instrumental platform and analyte class, the data acquired can represent a compromise between analyte extraction and spatial information. Here, we introduce an improvement to the spatial resolution achievable with MALDI MSI conducted with standard mass spectrometric systems that also reduces analyte migration during matrix application. Tissue is placed directly on a stretchable membrane that, when stretched, fragments the tissue into micrometer-sized pieces. Scanning electron microscopy analysis shows that this process produces fairly homogeneous distributions of small tissue fragments separated and surrounded by areas of hydrophobic membrane surface. MALDI matrix is then applied by either a robotic microspotter or an artist's airbrush. Rat spinal cord samples imaged with an instrumental resolution of 50-250 μm demonstrate lipid distributions with a 5-fold high spatial resolution (a 25-fold increase in pixel density) after stretching compared to tissues that were not stretched.
基质辅助激光解吸/电离(MALDI)质谱成像(MSI)将丰富的化学检测信息与分析物的空间定位相结合。对于给定的仪器平台和分析物类别,所获得的数据可以代表分析物提取和空间信息之间的折衷。在这里,我们介绍了一种改进,即在使用标准质谱系统进行 MALDI MSI 时,可以提高空间分辨率,同时减少基质施加过程中分析物的迁移。将组织直接放在可拉伸膜上,当拉伸时,组织会被切成微米大小的碎片。扫描电子显微镜分析表明,该过程产生的小组织碎片分布均匀,碎片被疏水膜表面的区域隔开和包围。然后通过机器人微点样器或艺术家喷枪施加 MALDI 基质。与未拉伸的组织相比,在仪器分辨率为 50-250 μm 的情况下对大鼠脊髓样本进行成像,拉伸后脂质分布的空间分辨率提高了 5 倍(像素密度增加了 25 倍)。