Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Denver, Anschutz Medical Campus , Aurora, Colorado 80045, United States.
Department of Chemistry, East Carolina University , Greenville, North Carolina 27858, United States.
Anal Chem. 2017 Jun 20;89(12):6384-6391. doi: 10.1021/acs.analchem.6b04628. Epub 2017 Jun 2.
A commercial liquid chromatography/drift tube ion mobility-mass spectrometer (LC/IM-MS) was evaluated for its utility in global metabolomics analysis. Performance was assessed using 12 targeted metabolite standards where the limit of detection (LOD), linear dynamic range, resolving power, and collision cross section (Ω) are reported for each standard. Data were collected in three different instrument operation modes: flow injection analysis with IM-MS (FIA/IM-MS), LC/MS, and LC/IM-MS. Metabolomics analyses of human plasma and HaCaT cells were used to compare the above three operation modes. LC/MS provides linearity in response, data processing automation, improved limits of detection, and ease of use. Advantages of LC/IM-MS and FIA/IM-MS include the ability to develop mobility-mass trend lines for structurally similar biomolecules, increased peak capacity, reduction of chemical/matrix noise, improvement in signal-to-noise, and separations of isobar/isomer compounds that are not resolved by LC. We further tested the feasibility of incorporating IM-MS into conventional LC/MS metabolomics workflows. In general, the addition of ion mobility dimension has increased the separation of compounds in complex biological matrixes and has the potential to largely improve the throughput of metabolomics analysis.
商业液相色谱/漂移管离子淌度-质谱联用仪(LC/IM-MS)在全球代谢组学分析中的应用效能进行了评估。采用 12 种靶向代谢物标准品对性能进行了评估,报告了每种标准品的检测限(LOD)、线性动态范围、分辨率和碰撞截面(Ω)。在三种不同的仪器操作模式下收集数据:带有 IM-MS 的流动注射分析(FIA/IM-MS)、LC/MS 和 LC/IM-MS。使用人血浆和 HaCaT 细胞的代谢组学分析比较了上述三种操作模式。LC/MS 提供了线性响应、数据处理自动化、提高了检测限和易用性。LC/IM-MS 和 FIA/IM-MS 的优势包括能够为结构相似的生物分子开发淌度-质量趋势线、增加峰容量、减少化学/基质噪声、提高信噪比以及分离 LC 无法分辨的等摩尔/异构体化合物。我们进一步测试了将 IM-MS 纳入常规 LC/MS 代谢组学工作流程的可行性。一般来说,离子淌度维度的增加增加了复杂生物基质中化合物的分离度,有可能大大提高代谢组学分析的通量。