Glutamine's role as an energetic fuel has been extensively studied in the past using I4C-and 3H-labeled tracers in cultured human cells. Yet another prominent role of glutamine, that of a nitrogen shuttle, cannot be approached without an N-tracer. We therefore used I5N-labeled glutamine and glutamat
A method for measuring both glutamine and glutamate levels and stable isotopic enrichments
β Scribed by D. Darmaun; M.J. Manary; D.E. Matthews
- Publisher
- Elsevier Science
- Year
- 1985
- Tongue
- English
- Weight
- 894 KB
- Volume
- 147
- Category
- Article
- ISSN
- 0003-2697
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β¦ Synopsis
A method is described for measuring separately ghuamine and glutamate levels and stable isotopic enrichment in plasma or whole blood samples by gas chromatography-mass spectrometry (GCMS). Deuterated internal standards are used for the quantitation via reverse isotope dilution and are added to plasma samples immediately upon sample collection. The samples are then applied to miniature anion-exchange columns to separate glutamine and glutamate, and the separated fractions are derivatized for GCMS analysis. The internal standards serve not only to quantitate both amino acids by reverse isotope dilution, but also to correct for glutamine deamidation to glutamate during sample storage and handling. Glutamine and glutamate are quantitated from plasma with typical precisions of 1 and 16%, respectively. Plasma glutamine and glutamate amino-15N enrichments are determined with precisions of 2 and 12%, respectively. The precision of the glutamate measurements for whole blood is typically 6%. where the glutamate levels are higher. This method uses inexpensive columns, allows simultaneous processing of multiple samples, and requires minimal volumes of plasma (250 ~1). ~1 1985 Academic Press, Inc.
π SIMILAR VOLUMES
Stable isotopes are commonly used as tracers for the measurement of glycerol and glucose kinetics in metabolic studies. Traditionally, the analysis of these isotopes has been performed using gas chromatographymass spectrometry, which requires that the analytes first be derivatized. The derivatizatio