Department of Chemistry, Texas A&M University, College Station, TX, 77843, USA.
J Am Soc Mass Spectrom. 2019 Jan;30(1):192-198. doi: 10.1007/s13361-018-1976-0. Epub 2018 May 23.
As a step towards development of a high-resolution ion mobility mass spectrometer using the orbitrap mass analyzer platform, we describe herein a novel reverse-entry ion source (REIS) coupled to the higher-energy C-trap dissociation (HCD) cell of an orbitrap mass spectrometer with extended mass range. Development of the REIS is a first step in the development of a drift tube ion mobility-orbitrap MS. The REIS approach retains the functionality of the commercial instrument ion source which permits the uninterrupted use of the instrument during development as well as performance comparisons between the two ion sources. Ubiquitin (8.5 kDa) and lipid binding to the ammonia transport channel (AmtB, 126 kDa) protein complex were used as model soluble and membrane proteins, respectively, to evaluate the performance of the REIS instrument. Mass resolution obtained with the REIS is comparable to that obtained using the commercial ion source. The charge state distributions for ubiquitin and AmtB obtained on the REIS are in agreement with previous studies which suggests that the REIS-orbitrap EMR retains native structure in the gas phase. Graphical Abstract ᅟ.
为了朝着使用轨道阱质量分析仪平台开发高分辨率离子淌度质谱仪的方向发展,我们在此描述了一种新颖的反向入口离子源(REIS),该离子源与轨道阱质量分析仪的更高能量 C-阱解离(HCD)单元耦合,扩展了质量范围。REIS 的开发是开发漂移管离子淌度-轨道阱 MS 的第一步。REIS 方法保留了商用仪器离子源的功能,这允许在开发过程中不间断地使用仪器,并可以对两种离子源的性能进行比较。分别使用 8.5 kDa 的泛素和与氨转运通道(AmtB,126 kDa)蛋白复合物结合的脂质作为模型可溶性和膜蛋白,以评估 REIS 仪器的性能。使用 REIS 获得的质量分辨率可与使用商用离子源获得的分辨率相媲美。在 REIS 上获得的泛素和 AmtB 的电荷状态分布与先前的研究一致,这表明 REIS-轨道阱 EMR 在气相中保留了天然结构。