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用于增强复杂肽检测和改善数据分析的半自动化液相色谱-质谱成像平台。

Semi-automated liquid chromatography-mass spectrometric imaging platform for enhanced detection and improved data analysis of complex peptides.

机构信息

School of Pharmacy, University of Wisconsin, 777 Highland Avenue, Madison, WI 53705, USA.

出版信息

J Chromatogr A. 2013 Jun 7;1293:44-50. doi: 10.1016/j.chroma.2013.03.042. Epub 2013 Mar 26.

Abstract

A semi-automated analytical platform featuring the coupling of monolithic reversed-phase liquid chromatography (RPLC) to matrix-assisted laser desorption/ionization mass spectrometric imaging (MALDI MSI) has been developed and evaluated. This is the first time that LC separation is readily coupled to MS imaging detection for the analysis of complex peptide mixtures both qualitatively and quantitatively. Methacrylate-based monolithic column with C12 functional groups is fabricated for fast RPLC separation. The LC flow and matrix flow are collected on a commercially available MALDI plate which is mechanically controlled and analyzed with MALDI MSI subsequently. Both tryptic peptides digested from bovine serum albumin (BSA) and endogenous neuropeptides extracted from the blue crab Callinectes sapidus are analyzed with this novel LC-MSI platform. Compared with regular offline LC fractionation coupled with MALDI MS detection, LC-MSI exhibits significantly increased MS signal intensity due to retaining of temporal resolution from separation dimension via continuous sampling, which results in increased number of peptides detected and accurate quantitation. In addition, imaging signals enable improved data analysis based on either mass-to-charge ratio or retention time, which is extremely beneficial for the analysis of complex analytes. These findings have demonstrated the potential of employing LC-MSI platform for enhanced proteomics and peptidomics studies.

摘要

我们开发并评估了一种半自动化分析平台,该平台的特点是将整体反相液相色谱 (RPLC) 与基质辅助激光解吸/电离质谱成像 (MALDI MSI) 相结合。这是首次将 LC 分离与 MS 成像检测直接耦合,用于对复杂肽混合物进行定性和定量分析。我们制备了带有 C12 官能团的甲基丙烯酸酯整体柱,用于快速 RPLC 分离。LC 流和基质流被收集在市售的 MALDI 板上,然后用 MALDI MSI 进行机械控制和分析。我们使用这种新型 LC-MSI 平台分析了来自牛血清白蛋白 (BSA) 的胰蛋白酶肽和来自蓝蟹 Callinectes sapidus 的内源性神经肽。与常规的离线 LC 馏分收集与 MALDI MS 检测相比,LC-MSI 由于通过连续采样从分离维度保留了时间分辨率,因此 MS 信号强度显著增加,从而增加了检测到的肽数量和准确的定量。此外,成像信号可以基于质荷比或保留时间进行改进数据分析,这对于分析复杂的分析物非常有益。这些发现表明,LC-MSI 平台在增强蛋白质组学和肽组学研究方面具有潜力。

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