Simultaneous quantification of malonyl-CoA and several other short-chain acyl-CoAs in animal tissues by ion-pairing reversed-phase HPLC/MS

J Chromatogr B Analyt Technol Biomed Life Sci. 2007 Jun 15;853(1-2):303-13. doi: 10.1016/j.jchromb.2007.03.029. Epub 2007 Mar 31.

Abstract

Malonyl-CoA is a key intermediate involved in lipid synthesis and lipid oxidation. Here, we report on a novel method for the quantification of malonyl-CoA and seven other short-chain acyl-CoAs in various rat and mouse tissues using ion-pairing reversed-phase HPLC/MS. This method is capable of measuring malonyl-CoA, free coenzyme A (CoASH), acetyl-CoA, beta-hydroxyl-butyryl-CoA (HB-CoA), 3-hydroxy-3-methyl-glutaryl-CoA (HMG-CoA), propionyl-CoA, succinyl-CoA, and isobutyryl-CoA simultaneously with a dynamic linear range over two orders of magnitude in a 7.0 min HPLC gradient run. The lower limit of quantification (LLOQ) was 0.225 pmol for all acyl-CoAs studied, except for HMG-CoA which had a higher LLOQ of 0.90 pmol. The interference of HB-CoA on the quantification of malonyl-CoA in animal tissues was also explored for the first time.

MeSH terms

  • Acetyl Coenzyme A / analysis
  • Acetyl Coenzyme A / chemistry
  • Acyl Coenzyme A / analysis*
  • Acyl Coenzyme A / chemistry
  • Animals
  • Chromatography, High Pressure Liquid / methods*
  • Liver / chemistry
  • Malonyl Coenzyme A / analysis*
  • Malonyl Coenzyme A / chemistry
  • Mice
  • Molecular Structure
  • Muscle, Skeletal / chemistry
  • Myocardium / chemistry
  • Rats
  • Rats, Sprague-Dawley
  • Reproducibility of Results

Substances

  • Acyl Coenzyme A
  • butyryl-coenzyme A
  • propionyl-coenzyme A
  • Malonyl Coenzyme A
  • Acetyl Coenzyme A
  • succinyl-coenzyme A