Journal
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES
Volume 877, Issue 1-2, Pages 43-49Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.jchromb.2008.11.018
Keywords
Derivatization; Tracer-tracee ratio; LC-MS/MS; Phenylalanine; Tyrosine; Stable isotope labeled amino acids; Protein turnover
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Whole-body protein synthesis and breakdown are measured by a combined tracer infusion protocol with the stable isotope amino acids L-[ring-(2)H(5)]-phenylalanine, L-[ring-(2)H(2)]-tyrosine and L-[ring-(2)H(4)]tyrosine that enable the measurement of the phenylalanine to tyrosine conversion rate. We describe a liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for the measurement of very low tracer-tracee ratios (TTR) of the amino acids L-phenylalanine and L-tyrosine in human plasma. TTR calibration curves of the tracers L-[rirlg-(2)H(5)]-phenylalanine, L-[ring-(2)H(2)]-tyrosine and L-[ring-(2)H(4)]-tyrosine were linear (r(2) > 0.99) ill the range between 0.01% and 5.0% TTR and lowest measurable TTR for the tracers was 0.01% at a physiological concentration of 60 [tM. The method was applied successfully to plasma samples from a clinical Study reaching a steady state enrichment plateau (mean +/- SD) of 3.33 +/- 0.19% for L-[ring-(2)H(5)]-phyenylanlanine, 2.40 +/- 0.43% for L-[ring-(2)H(2)]-tyrosine and 0.29 +/- 0.07% for L-[ring-(2)H(4)]-tyrosine, respectively. The LC-MS/MS method can be applied for measurement of very low plasma enrichments of phenylalanine and tyrosine for the determination of whole-body protein synthesis and breakdown rates in humans. Published by Elsevier B.V.
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