Published March 28, 2014 | Version v1
Journal article

Determination of energy metabolites in cancer cells by porous graphitic carbon liquid chromatography electrospray ionization mass spectrometry for the assessment of energy metabolism

  • 1. Laboratory of Environmental Chemistry and Bioanalytics, Department of Analytical Chemistry, Institute of Chemistry, Eötvös Loránd University, Pázmány Péter stny 1/A, H-1117 Budapest (Hungary)
  • 2. Institute of Analytical Chemistry and Food Chemistry, Graz University of Technology, Stremayrgasse 9, 8010 Graz (Austria)
  • 3. Research Centre for Natural Sciences of the Hungarian Academy of Sciences, Pusztaszeri u. 59-67, H-1025 Budapest (Hungary)
  • 4. 1st Institute of Pathology and Experimental Cancer Research, Semmelweis University, H-1085 Budapest (Hungary)

Description

Graphical abstract: - Highlights: • All types of sugar metabolites can be investigated in one run on graphitic stationary phase. • Method development for acidic metabolites of energy metabolism using a single LC–MS run. • Study of 15 acidic energy metabolites on a PGC column using common eluents. • Lactate, acidic amino acid, organic acid and sugar phosphate determination in a single run. • Metabolism of U-13C glucose and 1-13C acetate in ZR-75-1 cells studied. - Abstract: A high performance liquid chromatography (HPLC) tandem mass spectrometric (MS/MS) method has been developed for the simultaneous determination of fifteen glucose, or acetate derived metabolites isolated from tumor cells. Glycolytic and tricarboxylic acid (TCA) cycle metabolites as well as acidic amino acids were separated on a HPLC porous graphitic carbon (PGC) column and simultaneously determined by means of triple quadrupole MS/MS using multiple reaction monitoring (MRM). Target compounds were eluted within 10 min with 8% v/v formic acid as an electronic modifier added to a 4:1 v/v methanol water mobile phase. The calibration is linear in the 1–100 μM concentration range for each analyte. The limit of detection ranges between 0.39 and 2.78 μM for the analytes concerned. To test the PGC–HPLC–MS/MS method in metabolomic studies, ZR-75.1 human mammary adenocarcinoma cells were labeled with U-13C glucose or 1-13C acetate. Applying the MRM mode, the incorporation of 13C into metabolites, isolated from the tumor cells, and derived from glucose or acetate, could be properly identified

Availability note (English)

Available from http://dx.doi.org/10.1016/j.aca.2014.01.055

Additional details

Identifiers

DOI
10.1016/j.aca.2014.01.055;
PII
S0003-2670(14)00141-X;

Publishing Information

Journal Title
Analytica Chimica Acta
Journal Volume
819
Journal Page Range
p. 108-115
ISSN
0003-2670
CODEN
ACACAM

Optional Information

Copyright
Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.