Journal
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY
Volume 28, Issue 4, Pages 587-596Publisher
SPRINGER
DOI: 10.1007/s13361-017-1594-2
Keywords
Ion mobility; Native mass spectrometry; Native IM-MS; Collisional cross-section; Computational theory; Noncovalent complexes; Trajectory method
Funding
- National Science Foundation [OCI-0960354]
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Ion mobility-mass spectrometry (IM-MS) can be a powerful tool for determining structural information about ions in the gas phase, from small covalent analytes to large, native-like or denatured proteins and complexes. For large biomolecular ions, which may have a wide variety of possible gas-phase conformations and multiple charge sites, quantitative, physically explicit modeling of collisional cross sections (CCSs) for comparison to IMS data can be challenging and time-consuming. We present a trajectory method (TM) based CCS calculator, named Collidoscope, which utilizes parallel processing and optimized trajectory sampling, and implements both He and N-2 as collision gas options. Also included is a charge-placement algorithm for determining probable charge site configurations for protonated protein ions given an input geometry in pdb file format. Results from Collidoscope are compared with those from the current state-of-the-art CCS simulation suite, IMoS. Collidoscope CCSs are within 4% of IMoS values for ions with masses from similar to 18 Da to similar to 800 kDa. Collidoscope CCSs using X-ray crystal geometries are typically within a few percent of IM-MS experimental values for ions with mass up to similar to 3.5 kDa (melittin), and discrepancies for larger ions up to similar to 800 kDa (GroEL) are attributed in large part to changes in ion structure during and after the electrospray process. Due to its physically explicit modeling of scattering, computational efficiency, and accuracy, Collidoscope can be a valuable tool for IM-MS research, especially for large biomolecular ions.
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