| Literature DB >> 32483395 |
Qiushi Sun1, Teresa W-M Fan1,2,3, Andrew N Lane1,2,3, Richard M Higashi1,2,3.
Abstract
Metabolism is a complex network of compartmentalized and coupled chemical reactions, which often involve transfers of substructures of biomolecules, thus requiring metabolite substructures to be tracked. Stable isotope resolved metabolomics (SIRM) enables pathways reconstruction, even among chemically identical metabolites, by tracking the provenance of stable isotope-labeled substructures using NMR and ultrahigh resolution (UHR) MS. The latter can resolve and count isotopic labels in metabolites and can identify isotopic enrichment in substructures when operated in tandem MS mode. However, MS2 is difficult to implement with chromatography-based UHR-MS due to lengthy MS1 acquisition time that is required to obtain the molecular isotopologue count, which is further exacerbated by the numerous isotopologue source ions to fragment. We review here recent developments in tandem MS applications of SIRM to obtain more detailed information about isotopologue distributions in metabolites and their substructures.Entities:
Keywords: 13C/15N positional isotopologues; Ion chromatography; data independent MS2; multiplexed stable isotope resolved metabolomics (mSIRM); nucleotides; pathway reconstruction; ultra high-resolution FT-MS
Year: 2019 PMID: 32483395 PMCID: PMC7263348 DOI: 10.1016/j.trac.2019.115676
Source DB: PubMed Journal: Trends Analyt Chem ISSN: 0165-9936 Impact factor: 12.296