| Literature DB >> 28936476 |
Liulin Deng1, Yehia M Ibrahim1, Erin S Baker1, Noor A Aly1, Ahmed M Hamid1, Xing Zhang1, Xueyun Zheng1, Sandilya V B Garimella1, Ian K Webb1, Spencer A Prost1, Jeremy A Sandoval1, Randolph V Norheim1, Gordon A Anderson1, Aleksey V Tolmachev1, Richard D Smith1.
Abstract
Mass spectrometry (MS)-based multi-omic measurements, including proteomics, metabolomics, lipidomics, and glycomics, are increasingly transforming our ability to characterize and understand biological systems. Multi-omic analyses and the desire for comprehensive measurement coverage presently have limitations due to the chemical diversity and range of abundances of biomolecules in complex samples. Advances addressing these challenges increasingly are based upon the ability to quickly separate, react and otherwise manipulate sample components for analysis by MS. Here we report on a new approach using Structures for Lossless Ion Manipulations (SLIM) to enable long serpentine path ion mobility spectrometry (IMS) separations followed by MS analyses. This approach provides previously unachieved resolution for biomolecular species, in conjunction with more effective ion utilization, and a basis for greatly improved characterization of very small sample sizes.Entities:
Keywords: Ion Mobility Spectrometry; Isomers; Mass Spectrometry; Structures for Lossless Ion Manipulations (SLIM)
Year: 2016 PMID: 28936476 PMCID: PMC5603265 DOI: 10.1002/slct.201600460
Source DB: PubMed Journal: ChemistrySelect ISSN: 2365-6549 Impact factor: 2.109