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基质辅助激光解吸电离成像质谱法定量分析低分子化合物 - 教程综述。

Quantification of low molecular weight compounds by MALDI imaging mass spectrometry - A tutorial review.

机构信息

Institute of Bioanalytical Chemistry, Saarland University, 66123 Saarbrücken, Germany.

Institute of Bioanalytical Chemistry, Saarland University, 66123 Saarbrücken, Germany.

出版信息

Biochim Biophys Acta Proteins Proteom. 2017 Jul;1865(7):726-739. doi: 10.1016/j.bbapap.2016.12.011. Epub 2016 Dec 22.

DOI:10.1016/j.bbapap.2016.12.011
PMID:28012871
Abstract

Matrix-assisted laser desorption/ionization (MALDI)-mass spectrometry imaging (MSI) permits label-free in situ analysis of chemical compounds directly from the surface of two-dimensional biological tissue slices. It links qualitative molecular information of compounds to their spatial coordinates and distribution within the investigated tissue. MALDI-MSI can also provide the quantitative amounts of target compounds in the tissue, if proper calibration techniques are performed. Obviously, as the target molecules are embedded within the biological tissue environment and analysis must be performed at their precise locations, there is no possibility for extensive sample clean-up routines or chromatographic separations as usually performed with homogenized biological materials; ion suppression phenomena therefore become a critical side effect of MALDI-MSI. Absolute quantification by MALDI-MSI should provide an accurate value of the concentration/amount of the compound of interest in relatively small, well-defined region of interest of the examined tissue, ideally in a single pixel. This goal is extremely challenging and will not only depend on the technical possibilities and limitations of the MSI instrument hardware, but equally on the chosen calibration/standardization strategy. These strategies are the main focus of this article and are discussed and contrasted in detail in this tutorial review. This article is part of a Special Issue entitled: MALDI Imaging, edited by Dr. Corinna Henkel and Prof. Peter Hoffmann.

摘要

基质辅助激光解吸/电离(MALDI)-质谱成像(MSI)允许对二维生物组织切片表面的化合物进行无标记的原位分析。它将化合物的定性分子信息与其在研究组织中的空间坐标和分布联系起来。如果采用适当的校准技术,MALDI-MSI 还可以提供组织中目标化合物的定量含量。显然,由于目标分子嵌入在生物组织环境中,并且必须在其精确位置进行分析,因此没有可能进行广泛的样品净化程序或色谱分离,就像通常对均质生物材料进行的那样;因此,离子抑制现象成为 MALDI-MSI 的一个关键副作用。MALDI-MSI 的绝对定量应该在被检查组织的相对较小的、定义明确的感兴趣区域中提供感兴趣化合物的浓度/含量的准确值,理想情况下在单个像素中。这一目标极具挑战性,不仅取决于 MSI 仪器硬件的技术可能性和局限性,而且同样取决于所选择的校准/标准化策略。这些策略是本文的主要重点,并在本教程综述中进行了详细的讨论和对比。本文是题为“MALDI 成像”的特刊的一部分,由 Corinna Henkel 博士和 Peter Hoffmann 教授编辑。

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