Poltash Michael L, McCabe Jacob W, Shirzadeh Mehdi, Laganowsky Arthur, Russell David H
Department of Chemistry, Texas A&M University, 3255 TAMU, College Station, Texas 77843.
Trends Analyt Chem. 2020 Mar;124. doi: 10.1016/j.trac.2019.05.035. Epub 2019 May 31.
Native ion mobility-mass spectrometry (IM-MS) is an emerging biophysical approach to probe the intricate details of protein structure and function. The instrument design enables measurements of accurate first-principle determinations of rotationally-averaged ion-neutral collision cross sections coupled with high-mass, high-resolution mass measurement capabilities of Orbitrap MS. The inherent duty-cycle mismatch between drift tube IM and Orbitrap MS is alleviated by operating the drift tube in a frequency modulated mode while continuously acquiring mass spectra with the Orbitrap MS. Fourier transform of the resulting time-domain signal, i.e., ion abundances as a function of the modulation frequency, yields a frequency domain spectrum that is then converted (s to s) to IM drift time. This multiplexed approach allows for a duty-cycle of 25% compared to <1% for traditional "pulse-and-wait" IM-ToF-MS. Improvements in mobility and mass resolution of the IM-Orbitrap allows for accurate analysis of intact protein complexes and the possibility of capturing protein dynamics.
原生离子淌度-质谱联用(IM-MS)是一种新兴的生物物理方法,用于探究蛋白质结构和功能的复杂细节。该仪器设计能够测量旋转平均离子-中性碰撞截面的精确第一性原理测定值,并结合了Orbitrap质谱仪的高质量、高分辨率质量测量能力。通过在调频模式下操作漂移管,同时利用Orbitrap质谱仪连续采集质谱,缓解了漂移管离子淌度谱与Orbitrap质谱仪之间固有的占空比不匹配问题。对所得时域信号(即作为调制频率函数的离子丰度)进行傅里叶变换,得到频域谱,然后将其转换(秒到秒)为离子淌度漂移时间。与传统的“脉冲等待”IM-TOF-MS小于1%的占空比相比,这种复用方法允许25%的占空比。IM-Orbitrap在淌度和质量分辨率方面的改进,使得能够对完整的蛋白质复合物进行精确分析,并有可能捕捉蛋白质动力学。