化学
马尔迪成像
质谱成像
质谱法
显微镜
染色
污渍
基质辅助激光解吸/电离
样品制备
蛋白质组学
原位
分析化学(期刊)
色谱法
解吸
病理
生物化学
医学
有机化学
吸附
基因
作者
Pierre Chaurand,Sarah Schwartz,Dean Billheimer,Baogang Xu,Anna C. Crecelius,Richard M. Caprioli
摘要
MALDI (matrix-assisted laser desorption/ionization) imaging mass spectrometry (IMS) is a new technology that generates molecular profiles and two-dimensional ion density maps of peptide and protein signals directly from the surface of thin tissue sections. This allows specific information to be obtained on the relative abundance and spatial distribution of proteins. One important aspect of this is the opportunity to correlate these specific ion images with histological features observed by optical microscopy. To facilitate this, we have developed protocols that allow MALDI mass spectrometry imaging and optical microscopy to be performed on the same section. Key components of these protocols involve the use of conductive glass slides as sample support for the tissue sections and MS-friendly tissue staining protocols. We show the effectiveness of these with protein standards and with several types of tissue sections. Although stain-specific intensity variations occur, the overall protein pattern and spectrum quality remain consistent between stained and control tissue samples. Furthermore, imaging mass spectrometry experiments performed on stained sections showed good image quality with minimal delocalization of proteins resulting from the staining protocols.
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