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Precast Gelatin-Based Molds for Tissue Embedding Compatible with Mass Spectrometry Imaging

机译:适用于组织嵌入的基于明胶的预制模具与质谱成像兼容

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摘要

Preparation of tissue for matrix-assisted laser desorption ionization mass spectrometry imaging (MALDI-MSI) generally involves embedding the tissue followed by freezing and cryosectioning, usually between 5-25 μm thick, depending on the tissue type and the analyte(s) of interest. The brain is approximately 60% fat; it therefore lacks rigidity and poses structural preservation challenges during sample preparation. Histological sample preparation procedures are generally transferable to MALDI-MSI; however, there are various limitations. Optimal cutting temperature compound (OCT) is commonly used to embed and mount fixed tissue onto the chuck inside the cryostat during cryosectioning. However, OCT contains potential interferences that are detrimental to MALDI-MSI, whilst fixation is undesirable for the analysis of some analytes either due to extraction or chemical modification (i.e. polar metabolites). Therefore a method for both fixed and fresh tissue compatible with MALDI-MSI and histology is desirable to increase the breadth of analyte(s), maintain the topographies of the brain and provide rigidity to the fragile tissue whilst eliminating background interference. The method we introduce uses precast gelatin-based molds in which a whole mouse brain is embedded, flash frozen and cryosectioned in preparation for mass spectrometry imaging (MSI).
机译:制备用于基质辅助激光解吸电离质谱成像(MALDI-MSI)的组织通常涉及将组织包埋,然后冷冻和冷冻切片,通常厚度在5-25μm之间,具体取决于组织类型和感兴趣的分析物。大脑的脂肪约为60%;因此,它缺乏刚性,在样品制备过程中对结构保存提出了挑战。组织学样品制备程序通常可转移至MALDI-MSI;但是,存在各种限制。最佳切割温度化合物(OCT)通常用于在冷冻切片过程中将固定的组织嵌入并固定在低温恒温器内部的卡盘上。但是,OCT包含对MALDI-MSI有害的潜在干扰,而由于萃取或化学修饰(例如极性代谢物),固定对于分析某些分析物而言是不可取的。因此,需要一种与MALDI-MSI和组织学相容的固定和新鲜组织的方法,以增加分析物的广度,维持脑的拓扑结构并为脆弱的组织提供刚性,同时消除背景干扰。我们介绍的方法使用的是基于明胶的预制模具,其中嵌入了整个老鼠的大脑,进行了快速冷冻和冷冻切片,以准备进行质谱成像(MSI)。

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