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NMR Methods for Determining Lipid Turnover via Stable Isotope Resolved Metabolomics.
Lin, Penghui; Dai, Li; Crooks, Daniel R; Neckers, Leonard M; Higashi, Richard M; Fan, Teresa W-M; Lane, Andrew N.
Affiliation
  • Lin P; Center for Environmental and Systems Biochemistry, University of Kentucky, 789 S. Limestone St, Lexington, KY 40536, USA.
  • Dai L; Urologic Oncology Branch, Center for Cancer Research, NCI, NIH, Bethesda, MD 20892, USA.
  • Crooks DR; Urologic Oncology Branch, Center for Cancer Research, NCI, NIH, Bethesda, MD 20892, USA.
  • Neckers LM; Urologic Oncology Branch, Center for Cancer Research, NCI, NIH, Bethesda, MD 20892, USA.
  • Higashi RM; Center for Environmental and Systems Biochemistry, University of Kentucky, 789 S. Limestone St, Lexington, KY 40536, USA.
  • Fan TW; Department Toxicology & Cancer Biology, University of Kentucky, 789 S. Limestone St, Lexington, KY 40536, USA.
  • Lane AN; Center for Environmental and Systems Biochemistry, University of Kentucky, 789 S. Limestone St, Lexington, KY 40536, USA.
Metabolites ; 11(4)2021 Mar 29.
Article in En | MEDLINE | ID: mdl-33805301
ABSTRACT
Lipids comprise diverse classes of compounds that are important for the structure and properties of membranes, as high-energy fuel sources and as signaling molecules. Therefore, the turnover rates of these varied classes of lipids are fundamental to cellular function. However, their enormous chemical diversity and dynamic range in cells makes detailed analysis very complex. Furthermore, although stable isotope tracers enable the determination of synthesis and degradation of complex lipids, the numbers of distinguishable molecules increase enormously, which exacerbates the problem. Although LC-MS-MS (Liquid Chromatography-Tandem Mass Spectrometry) is the standard for lipidomics, NMR can add value in global lipid analysis and isotopomer distributions of intact lipids. Here, we describe new developments in NMR analysis for assessing global lipid content and isotopic enrichment of mixtures of complex lipids for two cell lines (PC3 and UMUC3) using both 13C6 glucose and 13C5 glutamine tracers.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Metabolites Year: 2021 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Metabolites Year: 2021 Type: Article Affiliation country: United States