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Ultra-High Mass Resolution MALDI Imaging Mass Spectrometry of Proteins and Metabolites in a Mouse Model of Glioblastoma

机译:胶质母细胞瘤小鼠模型中蛋白质和代谢物的超高质量分辨率MALDI成像蛋白质和代谢物

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摘要

Abstract MALDI mass spectrometry imaging is able to simultaneously determine the spatial distribution of hundreds of molecules directly from tissue sections, without labeling and without prior knowledge. Ultra-high mass resolution measurements based on Fourier-transform mass spectrometry have been utilized to resolve isobaric lipids, metabolites and tryptic peptides. Here we demonstrate the potential of 15T MALDI-FTICR MSI for molecular pathology in a mouse model of high-grade glioma. The high mass accuracy and resolving power of high field FTICR MSI enabled tumor specific proteoforms, and tumor-specific proteins with overlapping and isobaric isotopic distributions to be clearly resolved. The protein ions detected by MALDI MSI were assigned to proteins identified by region-specific microproteomics (0.8 mm2 regions isolated using laser capture microdissection) on the basis of exact mass and isotopic distribution. These label free quantitative experiments also confirmed the protein expression changes observed by MALDI MSI and revealed changes in key metabolic proteins, which were supported by in-situ metabolite MALDI MSI.
机译:摘要马尔迪质谱成像能够同时从组织切片同时测定数百分子的空间分布,而无需贴标签,没有先验知识。基于傅立叶变换质谱法的超高质量分辨率测量已被利用来解决异脂脂质,代谢物和胰蛋白肽。在这里,我们证明了在高级胶质瘤的小鼠模型中分子病理学的15T Maldi-FTICR MSI的潜力。高场FTICR MSI的高质量准确度和解决能力使肿瘤特异性蛋白质仿死,以及具有重叠和不均衡同位素分布的肿瘤特异性蛋白质可以清楚地解决。基于精确的质量和同位素分布,将MALDI MSI检测到的MALDI MSI检测到的蛋白质离子由区域特异性微蛋白质(使用激光捕获微碎裂分离的0.8mm 2区)。这些标签的免费定量实验还证实了MALDI MSI观察到的蛋白质表达变化,并揭示了关键代谢蛋白的变化,其由原位代谢物MALDI MSI支持。

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