Journal
TRAC-TRENDS IN ANALYTICAL CHEMISTRY
Volume 116, Issue -, Pages 308-315Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.trac.2019.04.010
Keywords
Ion mobility; Mass spectrometry; Trapped ion mobility spectrometry; Ultra-high resolution; PASEF; Tandem TIMS; Lipidomics; Proteomics; Isomers; Macromolecular assemblies
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Funding
- National Science Foundation Division of Chemistry, under CAREER award [CHE-1654274]
- Division of Molecular and Cellular Biosciences
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Ion Mobility Spectrometry (IMS) is a widely used technique for the post-ionization separation and structural characterization of biomolecules. Trapped IMS (TIMS) is a relatively recent advance in the field of linear IMS that has shown advantages for the study of biological problems when in tandem with mass spectrometry (TIMS-MS). TIMS's unique nature of holding ions using an electric field against a moving buffer gas allows for the tuning of the mobility separation by defining the scan rate as a function of the analytical challenge. TIMS can provide accurate CCS values (<0.2% RSD) and a high mobility resolving power (R up to 470). This recently commercialized technology has distinct analytical and structural biology applications. The present review focuses on advances in biological separations using TIMS-MS instrumentation for the case of isomer separations (e.g., lipids, epimers, topoisomers, positional PTMs), conformational states (e.g., peptides and proteins) and native macromolecular assemblies. (C) 2019 Elsevier B.V. All rights reserved.
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