Mahmud Iqbal, Wei Bo, Veillon Lucas, Tan Lin, Martinez Sara, Tran Bao, Raskind Alexander, de Jong Felice, Akbani Rehan, Weinstein John N, Beecher Chris, Lorenzi Philip L
Res Sq. 2024 Feb 1:rs.3.rs-3914827. doi: 10.21203/rs.3.rs-3914827/v1.
Ion suppression is a major problem in mass spectrometry (MS)-based metabolomics; it can dramatically decrease measurement accuracy, precision, and signal-to-noise sensitivity. Here we report a new method, the IROA TruQuant Workflow, that uses a stable isotope-labeled internal standard (IROA-IS) plus novel companion algorithms to 1) measure and correct for ion suppression, and 2) perform Dual MSTUS normalization of MS metabolomic data. We have evaluated the method across ion chromatography (IC), hydrophilic interaction liquid chromatography (HILIC), and reverse phase liquid chromatography (RPLC)-MS systems in both positive and negative ionization modes, with clean and unclean ion sources, and across different biological matrices. Across the broad range of conditions tested, all detected metabolites exhibited ion suppression ranging from 1% to 90+% and coefficient of variations ranging from 1% to 20%, but the Workflow and companion algorithms were highly effective at nulling out that suppression and error. Overall, the Workflow corrects ion suppression across diverse analytical conditions and produces robust normalization of non-targeted metabolomic data.
离子抑制是基于质谱(MS)的代谢组学中的一个主要问题;它会显著降低测量的准确性、精密度和信噪比灵敏度。在此,我们报告一种新方法——IROA TruQuant工作流程,该方法使用稳定同位素标记的内标(IROA-IS)以及新颖的配套算法,以:1)测量并校正离子抑制;2)对MS代谢组学数据进行双重MSTUS归一化。我们已在正离子和负离子模式下,针对具有清洁和不清洁离子源的离子色谱(IC)、亲水作用液相色谱(HILIC)和反相液相色谱(RPLC)-MS系统,以及不同生物基质,对该方法进行了评估。在测试的广泛条件范围内,所有检测到的代谢物的离子抑制范围为1%至90%以上,变异系数范围为1%至20%,但该工作流程和配套算法在消除这种抑制和误差方面非常有效。总体而言,该工作流程可校正不同分析条件下的离子抑制,并对非靶向代谢组学数据进行可靠的归一化。