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Comprehensive Determination of Amino Acids for Diagnosis of Inborn Errors of Metabolism

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Part of the book series: Methods in Molecular Biology ((MIMB,volume 603))

Abstract

Analysis of clinically relevant amino acids using ion-exchange chromatography coupled to photometric detection has been an indispensable component in the detection of inborn errors of metabolism for six decades. Detection of amino acids using mass spectrometry offers advantages in speed and analytic specificity. Employing methanol extraction and controlled butylation, C8 reversed-phase chromatography, and MS/MS detection, 32 amino acids are quantified in 20 min with clinically appropriate imprecision in plasma, urine, and CSF. Quantitation is linear to 1,000 µmol/L and limits of detection are at least 1.0 µmol/L. Important isobaric amino acids are distinguished by chromatography or by unique patterns of fragmentation following collision-induced dissociation. The technique employs commercially available reagents and may be expanded and customized for specific clinical or research settings.

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© 2010 Humana Press, a part of Springer Science+Business Media, LLC

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Dietzen, D.J., Weindel, A.L. (2010). Comprehensive Determination of Amino Acids for Diagnosis of Inborn Errors of Metabolism. In: Garg, U., Hammett-Stabler, C. (eds) Clinical Applications of Mass Spectrometry. Methods in Molecular Biology, vol 603. Humana Press. https://doi.org/10.1007/978-1-60761-459-3_3

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  • DOI: https://doi.org/10.1007/978-1-60761-459-3_3

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  • Publisher Name: Humana Press

  • Print ISBN: 978-1-60761-458-6

  • Online ISBN: 978-1-60761-459-3

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