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同一切片组织的质谱成像、激光捕获显微切割和 LC-MS/MS

Mass Spectrometry Imaging, Laser Capture Microdissection, and LC-MS/MS of the Same Tissue Section.

机构信息

Fondazione Pisana per la Scienza ONLUS , 56121 Pisa, Italy.

Department of Chemistry and Industrial Chemistry, University of Pisa , 56126 Pisa, Italy.

出版信息

J Proteome Res. 2017 Aug 4;16(8):2993-3001. doi: 10.1021/acs.jproteome.7b00284. Epub 2017 Jul 5.

Abstract

Mass spectrometry imaging (MSI) is able to simultaneously record the distributions of hundreds of molecules directly from tissue. Rapid direct tissue analysis is essential for MSI in order to maintain spatial localization and acceptable measurement times. The absence of an explicit analyte separation/purification step means MSI lacks the depth of coverage of LC-MS/MS. In this work, we demonstrate how atmospheric pressure MALDI-MSI enables the same tissue section to be first analyzed by MSI, to identify regions of interest that exhibit distinct molecular signatures, followed by localized proteomics analysis using laser capture microdissection isolation and LC-MS/MS.

摘要

质谱成像(MSI)能够直接从组织中同时记录数百种分子的分布。为了保持空间定位和可接受的测量时间,MSI 中快速直接的组织分析是必不可少的。由于没有明确的分析物分离/纯化步骤,因此 MSI 的覆盖深度不如 LC-MS/MS。在这项工作中,我们展示了常压 MALDI-MSI 如何能够首先对同一组织切片进行 MSI 分析,以识别表现出独特分子特征的感兴趣区域,然后使用激光捕获显微切割分离和 LC-MS/MS 进行局部蛋白质组学分析。

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