Huang Luojiao, Kim Yaejin, Balluff Benjamin, Cillero-Pastor Berta
Cell Biology-Inspired Tissue Engineering, Institute for Technology-Inspired Regenerative Medicine, Maastricht University, 6229ER Maastricht, Netherlands.
Maastricht MultiModal Molecular Imaging Institute, Division of Imaging Mass Spectrometry, Maastricht University, 6229ER Maastricht, Netherlands.
Anal Chem. 2025 May 27;97(20):10919-10928. doi: 10.1021/acs.analchem.5c02020. Epub 2025 May 12.
Matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI) allows spatial molecular profiling. Despite many successful applications, an appropriate control of technical variations is still lacking for result reproducibility assessment and for maximizing the MSI data quality. To address this, we introduce a novel quality control standard (QCS) design and data analysis pipeline accounting for variability due to sample preparation and instrument performance. Firstly, we created a tissue mimicking QCS consisting of propranolol in a gelatin matrix. We showed that this QCS mimics ion suppression of propranolol in the tissue. Next, a three-day batch experiment demonstrated the QCS's performance to longitudinal technical variations, establishing it as an effective indicator of batch effects. Then three computational approaches for batch effect correction were applied for the first time to MALDI-MSI data, leading to a significant reduction of QCS variation and to improved sample clustering by using multivariate principal component analysis. Altogether, we offer the designed QCS in combination with a data correction pipeline for MALDI-MSI users for batch effect evaluation and correction.
基质辅助激光解吸/电离质谱成像(MALDI-MSI)可实现空间分子剖析。尽管有许多成功的应用,但在结果重现性评估和最大化MSI数据质量方面,仍缺乏对技术变异的适当控制。为了解决这一问题,我们引入了一种新颖的质量控制标准(QCS)设计和数据分析流程,以考虑样本制备和仪器性能导致的变异性。首先,我们创建了一种由普萘洛尔在明胶基质中组成的组织模拟QCS。我们表明,这种QCS模拟了组织中普萘洛尔的离子抑制。接下来,一项为期三天的批次实验证明了QCS对纵向技术变异的性能,将其确立为批次效应的有效指标。然后,首次将三种批次效应校正的计算方法应用于MALDI-MSI数据,通过使用多变量主成分分析,显著降低了QCS变异并改善了样本聚类。总之,我们为MALDI-MSI用户提供了设计的QCS与数据校正流程相结合的方法,用于批次效应评估和校正。