Quantification of L‐tryptophan and L‐kynurenine by liquid chromatography/electron capture negative ion chemical ionization mass spectrometry

R. L. Boni, J. T. Simpson, D. B. Naritsin, Kuniaki Saito, S. P. Markey

Research output: Contribution to journalArticle

14 Citations (Scopus)

Abstract

In a number of infectious and inflammatory diseases, stimulation of the immune system can lead to increased accumulation of tryptophan metabolites via induction of kynurenine pathway enzymes in extrahepatic tissues. We developed a liquid chromatographic/mass spectrometric (LC/MS) method suitable for tracing the disposition of 13C isotopomers of L‐tryptophan and L‐kynurenine in various cultured cell, tissue slice, and whole animal model systems used to investigate tryptophan flux through the kynurenine pathway. The method employs extractive derivatization of the analytes and their 2H internal standards with pentafluorobenzyl bromide in order to enhance the negative ion chemical ionization (NICI) mass spectrometric response. Normal‐phase liquid chromatographic separation of derivatized analytes was optimized using a silica column with organic solvents, followed by particle beam transfer and NICI‐MS. Standard curves were linear over the range 1–250 ng per sample. Particle beam and mass spectrometric operating parameters were optimized with direct flow injections of 1‐(methylamino) anthra‐quinone, which is an ideal test compound for the evaluation of LC/NICI‐MS. The developed method was used to quantify the conversion of (13C6)L‐tryptophan to (13C6)L‐kynurenine by human monocytes (THP‐1) stimulated with interferon‐γ, lung and brain tissue slices obtained from gerbils immune‐stimulated with pokeweed mitogen. The effect of whole body immune stimulation on the plasma levels of engogenous L‐kynurenine in mice stimulated with interferon‐γ was also quantified.

Original languageEnglish
Pages (from-to)27-32
Number of pages6
JournalBiological Mass Spectrometry
Volume23
Issue number1
DOIs
Publication statusPublished - 01-01-1994
Externally publishedYes

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Liquid chromatography
Liquid Chromatography
Ionization
Kynurenine
Mass spectrometry
Mass Spectrometry
Particle beams
Negative ions
Electrons
Ions
Tissue
Tryptophan
Interferons
Pokeweed Mitogens
Anthraquinones
Gerbillinae
Immune system
Immune System Diseases
Liquids
Metabolites

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Molecular Medicine

Cite this

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abstract = "In a number of infectious and inflammatory diseases, stimulation of the immune system can lead to increased accumulation of tryptophan metabolites via induction of kynurenine pathway enzymes in extrahepatic tissues. We developed a liquid chromatographic/mass spectrometric (LC/MS) method suitable for tracing the disposition of 13C isotopomers of L‐tryptophan and L‐kynurenine in various cultured cell, tissue slice, and whole animal model systems used to investigate tryptophan flux through the kynurenine pathway. The method employs extractive derivatization of the analytes and their 2H internal standards with pentafluorobenzyl bromide in order to enhance the negative ion chemical ionization (NICI) mass spectrometric response. Normal‐phase liquid chromatographic separation of derivatized analytes was optimized using a silica column with organic solvents, followed by particle beam transfer and NICI‐MS. Standard curves were linear over the range 1–250 ng per sample. Particle beam and mass spectrometric operating parameters were optimized with direct flow injections of 1‐(methylamino) anthra‐quinone, which is an ideal test compound for the evaluation of LC/NICI‐MS. The developed method was used to quantify the conversion of (13C6)L‐tryptophan to (13C6)L‐kynurenine by human monocytes (THP‐1) stimulated with interferon‐γ, lung and brain tissue slices obtained from gerbils immune‐stimulated with pokeweed mitogen. The effect of whole body immune stimulation on the plasma levels of engogenous L‐kynurenine in mice stimulated with interferon‐γ was also quantified.",
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Quantification of L‐tryptophan and L‐kynurenine by liquid chromatography/electron capture negative ion chemical ionization mass spectrometry. / Boni, R. L.; Simpson, J. T.; Naritsin, D. B.; Saito, Kuniaki; Markey, S. P.

In: Biological Mass Spectrometry, Vol. 23, No. 1, 01.01.1994, p. 27-32.

Research output: Contribution to journalArticle

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T1 - Quantification of L‐tryptophan and L‐kynurenine by liquid chromatography/electron capture negative ion chemical ionization mass spectrometry

AU - Boni, R. L.

AU - Simpson, J. T.

AU - Naritsin, D. B.

AU - Saito, Kuniaki

AU - Markey, S. P.

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