Center for Innovative Technology, Department of Chemistry, Vanderbilt Institute of Chemical Biology, Vanderbilt Institute for Integrative Biosystems Research and Education, Vanderbilt-Ingram Cancer Center, Vanderbilt University, Nashville, Tenessee 37235, United States.
MOBILion Systems, Chadds Ford, Pennsylvania 19317, United States.
J Am Soc Mass Spectrom. 2021 Apr 7;32(4):1126-1137. doi: 10.1021/jasms.1c00056. Epub 2021 Mar 18.
A production prototype structures for lossless ion manipulation ion mobility (SLIM IM) platform interfaced to a commercial high-resolution mass spectrometer (MS) is described. The SLIM IM implements the traveling wave ion mobility technique across a ∼13m path length for high-resolution IM (HRIM) separations. The resolving power (CCS/ΔCCS) of the SLIM IM stage was benchmarked across various parameters (traveling wave speeds, amplitudes, and waveforms), and results indicated that resolving powers in excess of 200 can be accessed for a broad range of masses. For several cases, resolving powers greater than 300 were achieved, notably under wave conditions where ions transition from a nonselective "surfing" motion to a mobility-selective ion drift, that corresponded to ion speeds approximately 30-70% of the traveling wave speed. The separation capabilities were evaluated on a series of isomeric and isobaric compounds that cannot be resolved by MS alone, including reversed-sequence peptides (SDGRG and GRGDS), triglyceride double-bond positional isomers (TG 3, 6, 9 and TG 6, 9, 12), trisaccharides (melezitose, raffinose, isomaltotriose, and maltotriose), and ganglioside lipids (GD1b and GD1a). The SLIM IM platform resolved the corresponding isomeric mixtures, which were unresolvable using the standard resolution of a drift-tube instrument (∼50). In general, the SLIM IM-MS platform is capable of resolving peaks separated by as little as ∼0.6% without the need to target a specific separation window or drift time. Low CCS measurement biases <0.5% were obtained under high resolving power conditions. Importantly, all the analytes surveyed are able to access high-resolution conditions (>200), demonstrating that this instrument is well-suited for broadband HRIM separations important in global untargeted applications.
一种用于无损离子操控离子淌度(SLIM IM)平台的生产原型结构与商业高分辨率质谱仪(MS)接口,该平台被描述。SLIM IM 在约 13m 的路径长度上实现了行波离子淌度技术,用于高分辨率 IM(HRIM)分离。SLIM IM 级别的分辨率(CCS/ΔCCS)在各种参数(行波速度、幅度和波形)下进行了基准测试,结果表明,对于广泛的质量范围,可以达到超过 200 的分辨率。在几种情况下,实现了超过 300 的分辨率,特别是在行波条件下,离子从非选择性的“冲浪”运动过渡到流动性选择性离子漂移,这对应于离子速度大约为行波速度的 30-70%。在一系列仅通过 MS 无法分离的异构体和等摩尔化合物上评估了分离能力,包括反向序列肽(SDGRG 和 GRGDS)、甘油三酯双键位置异构体(TG 3,6,9 和 TG 6,9,12)、三糖(蜜二糖、棉子糖、异麦芽三糖和麦芽三糖)和神经节苷脂脂质(GD1b 和 GD1a)。SLIM IM 平台解析了相应的异构体混合物,这些混合物在使用漂移管仪器的标准分辨率(约 50)时无法分离。一般来说,SLIM IM-MS 平台能够分辨出间隔仅为约 0.6%的峰,而无需针对特定的分离窗口或漂移时间。在高分辨率条件下,CCS 测量偏差<0.5%。重要的是,所有被调查的分析物都能够达到高分辨率条件(>200),这表明该仪器非常适合于全球无目标应用中重要的宽带 HRIM 分离。