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Li, J.* ; Hoene, M. ; Zhao, X.J.* ; Chen, S.L.* ; Wei, H.* ; Häring, H.-U. ; Lin, X.H.* ; Zeng, Z.D.* ; Weigert, C. ; Lehmann, R. ; Xu, G.W.*

Stable isotope-assisted lipidomics combined with nontargeted isotopomer filtering, a tool to unravel the complex dynamics of lipid metabolism.

Anal. Chem. 85, 4651-4657 (2013)
DOI PMC
Open Access Green as soon as Postprint is submitted to ZB.
Investigations of complex metabolic mechanisms and networks have become a focus of research in the postgenomic area, thereby creating an increasing demand for sophisticated analytical approaches. One such tool is lipidomics analysis that provides, a detailed picture of the lipid composition of a system at a given time Introducing stable isotopes into the studied system can additionally provide information on the synthesis, transformation and degradation of individual lipid species. However, capturing the entire dynamics of lipid networks is still a challenge. We developed and evaluated a novel strategy for the in-depth analysis of the dynamics of lipid metabolism with the capacity for high molecular specificity and network coverage. The general workflow consists of stable isotope-labeling experiments, ultrahigh-performance liquid chromatography (UHPLC)/high-resolution Orbitrap-mass spectrometry (MS) lipid profiling and data processing by a software tool for global isotopomer filtering and matching. As a proof of concept, this approach was applied to the network-wide mapping of dynamic lipid metabolism in primary human skeletal muscle cells cultured for 4, 12, and 24 h with [U-C-13]-palmitate. In the myocellular lipid extracts, 692 isotopomers were detected that could be assigned to 203 labeled lipid species spanning 12 lipid (sub)classes. Interestingly, some lipid classes showed high turnover rates but stable total amounts while the amount of others increased in the course of palmitate treatment. The novel strategy presented here has the potential to open new detailed insights into the dynamics of lipid metabolism that may lead to a better understanding of physiological mechanisms and metabolic perturbations.
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Publication type Article: Journal article
Document type Scientific Article
Keywords Chromatography/tandem Mass-spectrometry ; In-vivo ; Insulin-resistance ; Human Myotubes ; Fatty-acids ; Muscle ; Metabolomics ; Ceramides ; Database ; Lipotoxicity
Language english
Publication Year 2013
HGF-reported in Year 2013
ISSN (print) / ISBN 0003-2700
e-ISSN 1520-6882
Quellenangaben Volume: 85, Issue: 9, Pages: 4651-4657 Article Number: , Supplement: ,
Publisher American Chemical Society (ACS)
Reviewing status Peer reviewed
POF-Topic(s) 90000 - German Center for Diabetes Research
Research field(s) Helmholtz Diabetes Center
PSP Element(s) G-502400-001
PubMed ID 23537127
Erfassungsdatum 2013-06-29