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Applications of chromatography-ultra high-resolution MS for stable isotope-resolved metabolomics (SIRM) reconstruction of metabolic networks

机译:色谱 - 超高分辨率MS用于稳定同位素分辨的代谢组学(标准)重建代谢网络的研究

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摘要

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. (C) 2019 Elsevier B.V. All rights reserved.
机译:新陈代谢是划分和偶联的化学反应的复杂网络,其通常涉及生物分子的子结构的转移,从而需要跟踪代谢物子结构。稳定的同位素已解决的代谢组学(标准)通过使用NMR和超高分辨率(UHR)MS跟踪稳定同位素标记的子结构的出现,使途径重建能够重建,即使是化学相同的代谢物。后者可以在代谢物中解析和计数同位素标记,并且可以在串联MS模式下操作时识别子结构中的同位素富集。然而,由于在获得分子同位素计数所需的冗长MS1采集时间,MS 2难以使用基于色谱的UHR-MS实现,这将被许多同位素源离子进一步加剧至片段。我们在此审查了最近的SIRM中的MS应用中的最新进展,以获得更多关于代谢物及其子结构的同位素分布的更详细信息。 (c)2019年Elsevier B.V.保留所有权利。

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