La Rocca Raphaël, Kune Christopher, Tiquet Mathieu, Stuart Lachlan, Eppe Gauthier, Alexandrov Theodore, De Pauw Edwin, Quinton Loïc
Mass Spectrometry Laboratory, MolSys Research Unit, Department of Chemistry, University of Liège, Allée du Six Août, 11, Quartier Agora, Liège 4000, Belgium.
Structural and Computational Biology Unit, European Molecular Biology Laboratory, Heidelberg 69117, Germany.
Anal Chem. 2021 Mar 2;93(8):4066-4074. doi: 10.1021/acs.analchem.0c05071. Epub 2021 Feb 14.
Mass spectrometry imaging (MSI) is a powerful and convenient method for revealing the spatial chemical composition of different biological samples. Molecular annotation of the detected signals is only possible if a high mass accuracy is maintained over the entire image and the / range. However, the change in the number of ions from pixel-to-pixel of the biological samples could lead to small fluctuations in the detected /-values, called mass shift. The use of internal calibration is known to offer the best solution to avoid, or at least to reduce, mass shifts. Their "a priori" selection for a global MSI acquisition is prone to false positive detection and therefore to poor recalibration. To fill this gap, this work describes an algorithm that recalibrates each spectrum individually by estimating its mass shift with the help of a list of pixel-specific internal calibrating ions, automatically generated in a data-adaptive manner (https://github.com/LaRoccaRaphael/MSI_recalibration). Through a practical example, we applied the methodology to a zebrafish whole-body section acquired at a high mass resolution to demonstrate the impact of mass shift on data analysis and the capability of our algorithm to recalibrate MSI data. In addition, we illustrate the broad applicability of the method by recalibrating 31 different public MSI data sets from METASPACE from various samples and types of MSI and show that our recalibration significantly increases the numbers of METASPACE annotations (gaining from 20 up to 400 additional annotations), particularly the high-confidence annotations with a low false discovery rate.
质谱成像(MSI)是一种用于揭示不同生物样本空间化学成分的强大且便捷的方法。只有在整个图像和质量范围内保持高质谱精度,才有可能对检测到的信号进行分子注释。然而,生物样本中像素间离子数量的变化可能导致检测到的质荷比(m/z)值出现小的波动,即所谓的质量偏移。已知使用内部校准可提供最佳解决方案,以避免或至少减少质量偏移。在全局MSI采集时对其进行“先验”选择容易出现假阳性检测,从而导致校准不佳。为填补这一空白,本文描述了一种算法,该算法借助以数据自适应方式自动生成的特定像素内部校准离子列表来估计每个光谱的质量偏移,从而对每个光谱进行单独校准(https://github.com/LaRoccaRaphael/MSI_recalibration)。通过一个实际例子,我们将该方法应用于以高质谱分辨率采集的斑马鱼全身切片,以证明质量偏移对数据分析的影响以及我们算法重新校准MSI数据的能力。此外,我们通过重新校准来自METASPACE的31个不同的公共MSI数据集(这些数据集来自各种样本和MSI类型)来说明该方法的广泛适用性,并表明我们的重新校准显著增加了METASPACE注释的数量(从额外增加20个到400个注释),特别是具有低错误发现率的高置信度注释。