Dodds James N, Ford Lucie C, Ryan Jack P, Solosky Amie M, Rusyn Ivan, Baker Erin S
Department of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27514, United States.
Department of Veterinary Physiology and Pharmacology, Texas A&M University, College Station, Texas 77843, United States.
J Am Soc Mass Spectrom. 2025 Jul 2;36(7):1456-1466. doi: 10.1021/jasms.5c00056. Epub 2025 Apr 3.
As ion mobility spectrometry (IMS) separations continue to be added to analytical workflows due to their power in environmental and biological sample analyses, harmonization and capability understanding between existing and newly released instruments are desperately needed. Developments in IMS platforms often exhibit focus on increasing resolving power (R) to better separate molecules of similar structure. While the additional separation capacity is advantageous, ensuring these developments coincide with appropriate data extraction and analysis methods is imperative to ensure routine adoption. Herein, we assess the performance of the MOBILion MOBIE in relation to a commercially available drift tube IMS-MS, the Agilent 6560, and evaluate feature extraction and analysis pipelines. Both instruments were operated using matched conditions when possible, and performance metrics of scan speed, R, limits of detection (LOD), and propensity for isomer separation via LC-IMS-MS were evaluated. Similar scan speeds pertaining to IMS-MS frame generation were noted for both platforms, and collision cross section (CCS) values for the MOBIE were generally within ≤ 1% difference from previously reported drift tube values. Both platforms were also able to generate quantitative data (comparable limits of detection) in experiments with perfluoroalkyl substances (PFAS) mixtures in a cell-based model (both medium and cell lysates), as demonstrated in Skyline with adjusted mobility filtering parameters. Higher R was, however, noted on the MOBIE in comparison to the 6560 (200-300 vs 45-60 CCS/ΔCCS without data processing), allowing the detection of more PFAS isomers and indicating promise toward future applications in chemical exposomics studies and biomarker discovery when molecules exhibit similar structures.
随着离子迁移谱(IMS)分离技术因其在环境和生物样品分析中的强大功能而不断被纳入分析工作流程,现有仪器与新发布仪器之间的协调以及对其性能的了解变得迫切需要。IMS平台的发展通常侧重于提高分辨率(R),以更好地分离结构相似的分子。虽然额外的分离能力是有利的,但确保这些发展与适当的数据提取和分析方法相一致对于确保常规应用至关重要。在此,我们评估了MOBILion MOBIE相对于市售漂移管IMS-MS(安捷伦6560)的性能,并评估了特征提取和分析流程。两台仪器在可能的情况下都在匹配条件下运行,并评估了扫描速度、分辨率、检测限(LOD)以及通过LC-IMS-MS进行异构体分离的倾向等性能指标。两个平台在IMS-MS帧生成方面的扫描速度相似,并且MOBIE的碰撞截面(CCS)值与先前报道的漂移管值的差异通常≤1%。在基于细胞的模型(培养基和细胞裂解物)中使用全氟烷基物质(PFAS)混合物进行的实验中,两个平台也都能够生成定量数据(检测限相当),如在Skyline中通过调整迁移率过滤参数所证明的那样。然而,与6560相比,MOBIE的分辨率更高(未经数据处理时为200 - 300 vs 45 - 60 CCS/ΔCCS),这使得能够检测到更多的PFAS异构体,并表明在分子结构相似的化学暴露组学研究和生物标志物发现的未来应用中有潜力。