| Literature DB >> 32189816 |
Michael L Poltash1, Jacob W McCabe1, Mehdi Shirzadeh1, Arthur Laganowsky1, David H Russell1.
Abstract
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-1 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.Entities:
Keywords: Fourier transform-ion mobility; Ion mobility-mass spectrometry; Orbitrap mass spectrometer; high resolution mass spectrometry; intact protein complexes; ion mobility; membrane protein; native mass spectrometry; periodic focusing drift tube ion mobility; protein-ligand interactions
Year: 2019 PMID: 32189816 PMCID: PMC7079669 DOI: 10.1016/j.trac.2019.05.035
Source DB: PubMed Journal: Trends Analyt Chem ISSN: 0165-9936 Impact factor: 12.296