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Multimodal Mass Spectrometry Imaging of N-Glycans and Proteins from the Same Tissue Section

机译:来自同一组织切片的N-聚糖和蛋白质的多峰质谱成像

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摘要

On-tissue digestion matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI) can be used to record spatially correlated molecular information from formalin-fixed, paraffin-embedded (FFPE) tissue sections. In this work, we present the in situ multimodal analysis of N-linked glycans and proteins from the same FFPE tissue section. The robustness and applicability of the method are demonstrated for several tumors, including epithelial and mesenchymal tumor types. Major analytical aspects, such as lateral diffusion of the analyte molecules and differences in measurement sensitivity due to the additional sample preparation methods, have been investigated for both N-glycans and proteolytic peptides. By combining the MSI approach with extract analysis, we were also able to assess which mass spectral peaks generated by MALDI-MSI could be assigned to unique N-glycan and peptide identities.
机译:组织消化基质辅助激光解吸/电离质谱成像(MALDI-MSI)可用于记录福尔马林固定,石蜡包埋(FFPE)组织切片中与空间相关的分子信息。在这项工作中,我们提出了来自同一FFPE组织切片的N-连接聚糖和蛋白质的原位多峰分析。该方法的鲁棒性和适用性已被证明适用于多种肿瘤,包括上皮和间质肿瘤类型。对于N-聚糖和蛋白水解肽,已经研究了主要的分析方面,例如分析物分子的横向扩散以及由于其他样品制备方法而导致的测量灵敏度差异。通过将MSI方法与提取物分析相结合,我们还能够评估MALDI-MSI产生的质谱峰可以分配给唯一的N-聚糖和肽身份。

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