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A Proof of Concept to Bridge the Gap between Mass Spectrometry Imaging Protein Identification and Relative Quantitation: MSI~LC-MS/MS-LF

机译:弥合质谱成像蛋白质鉴定和相对定量之间差距的概念证明:MSI〜LC-MS / MS-LF

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摘要

Mass spectrometry imaging (MSI) is a powerful tool to visualize the spatial distribution of molecules on a tissue section. The main limitation of MALDI-MSI of proteins is the lack of direct identification. Therefore, this study focuses on a MSI~LC-MS/MS-LF workflow to link the results from MALDI-MSI with potential peak identification and label-free quantitation, using only one tissue section. At first, we studied the impact of matrix deposition and laser ablation on protein extraction from the tissue section. Then, we did a back-correlation of the m/z of the proteins detected by MALDI-MSI to those identified by label-free quantitation. This allowed us to compare the label-free quantitation of proteins obtained in LC-MS/MS with the peak intensities observed in MALDI-MSI. We managed to link identification to nine peaks observed by MALDI-MSI. The results showed that the MSI~LC-MS/MS-LF workflow (i) allowed us to study a representative muscle proteome compared to a classical bottom-up workflow; and (ii) was sparsely impacted by matrix deposition and laser ablation. This workflow, performed as a proof-of-concept, suggests that a single tissue section can be used to perform MALDI-MSI and protein extraction, identification, and relative quantitation.
机译:质谱成像(MSI)是一种强大的工具,可以可视化组织切片上分子的空间分布。蛋白质的MALDI-MSI的主要局限在于缺乏直接鉴定。因此,本研究着重于MSI〜LC-MS / MS-LF工作流程,以仅使用一个组织切片将MALDI-MSI的结果与潜在峰鉴定和无标记定量联系起来。首先,我们研究了基质沉积和激光烧蚀对从组织切片提取蛋白质的影响。然后,我们对MALDI-MSI检测到的蛋白质的m / z与无标记定量鉴定出的蛋白质的m / z进行了反相关。这使我们能够将LC-MS / MS中获得的蛋白质的无标记定量与MALDI-MSI中观察到的峰强度进行比较。我们设法将鉴定与MALDI-MSI观察到的九个峰相关联。结果表明,MSI〜LC-MS / MS-LF工作流程(i)与传统的自下而上的工作流程相比,使我们能够研究代表性的蛋白质组。 (ii)很少受到基质沉积和激光烧蚀的影响。作为概念验证执行的此工作流程表明,可以使用单个组织切片执行MALDI-MSI和蛋白质提取,鉴定和相对定量。

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