Literature DB >> 11916317

Prolidase deficiency diagnosed by 1H NMR spectroscopy of urine.

S H Moolenaar1, U F Engelke, N G Abeling, H Mandel, M Duran, R A Wevers.   

Abstract

Three urine samples from two prolidase-deficient patients were analysed using 1H NMR spectroscopy. One-dimensional 1H NMR spectra showed a characteristic pattern of overlapping resonances of the proline and hydroxyproline protons of the imidodipeptides. The model compounds Ala-Pro, Gly-Pro, Phe-Pro, Leu-Pro, Val-Pro, Gly-Hyp and Pro-Hyp were measured as well. The non-proline resonances of Val-Pro, Ala-Pro and Gly-Pro could be assigned in the urine spectra. These resonances could then be used for quantification of the corresponding imidodipeptids. The presence of Leu-Pro in the patients' urine was demonstrated by the results of COSY experiments. However, this imidodipeptide could not be quantified owing to overlap of the resonaces in the one-dimensional 1H NMR spectrum of the patients' urine. Phe-Pro, Pro-Hyp and Gly-Hyp could not be assigned in the spectrum of the patient's urine. The characteristic resonances in the urine from a prolidase-deficient patient, i.e. Ala-Pro, Val-Pro, Gly-Pro, and resonances of the (hydroxy)proline part of the imidodipeptides can be used to diagnose this disease.

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Year:  2001        PMID: 11916317     DOI: 10.1023/a:1013940207973

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  20 in total

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Authors:  S H Moolenaar; M S van der Knaap; U F Engelke; P J Pouwels; F S Janssen-Zijlstra; N M Verhoeven; C Jakobs; R A Wevers
Journal:  NMR Biomed       Date:  2001-05       Impact factor: 4.044

2.  3-Hydroxy-3-methylglutaryl-CoA lyase deficiency studied using 2-dimensional proton nuclear magnetic resonance spectroscopy.

Authors:  R A Iles; J R Jago; S R Williams; R A Chalmers
Journal:  FEBS Lett       Date:  1986-07-14       Impact factor: 4.124

3.  Use of capillary zone electrophoresis for analysis of imidodipeptides in urine of prolidase-deficient patients.

Authors:  G Zanaboni; R Grimm; K M Dyne; A Rossi; G Cetta; P Iadarola
Journal:  J Chromatogr B Biomed Appl       Date:  1996-08-09

4.  Analysis of biological fluids using 600 MHz proton NMR spectroscopy: application of homonuclear two-dimensional J-resolved spectroscopy to urine and blood plasma for spectral simplification and assignment.

Authors:  P J Foxall; J A Parkinson; I H Sadler; J C Lindon; J K Nicholson
Journal:  J Pharm Biomed Anal       Date:  1993-01       Impact factor: 3.935

5.  Clinical and biochemical characteristics of prolidase deficiency in siblings.

Authors:  B J Freij; H L Levy; G Dudin; D Mutasim; M Deeb; V M Der Kaloustian
Journal:  Am J Med Genet       Date:  1984-11

6.  The use of liquid chromatography-mass spectrometry for the identification and quantification of urinary iminodipeptides in prolidase deficiency.

Authors:  K Sugahara; T Ohno; J Arata; H Kodama
Journal:  Eur J Clin Chem Clin Biochem       Date:  1993-05

7.  Prolidase deficiency: a patient without hydroxyproline-containing iminodipeptides in urine.

Authors:  S J Wysocki; R Hahnel; T Mahoney; R G Wilson; P K Panegyres
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982

8.  Investigation of urea cycle enzyme disorders by 1H-NMR spectroscopy.

Authors:  S P Burns; D A Woolf; J V Leonard; R A Iles
Journal:  Clin Chim Acta       Date:  1992-07-31       Impact factor: 3.786

9.  Increased manganese content and reduced arginase activity in erythrocytes of a patient with prolidase deficiency (iminodipeptiduria).

Authors:  I Lombeck; U Wendel; J Versieck; L van Ballenberghe; H J Bremer; R Duran; S Wadman
Journal:  Eur J Pediatr       Date:  1986-04       Impact factor: 3.183

10.  Proton NMR spectroscopic analysis of multiple acyl-CoA dehydrogenase deficiency--capacity of the choline oxidation pathway for methylation in vivo.

Authors:  S P Burns; H C Holmes; R A Chalmers; A Johnson; R A Iles
Journal:  Biochim Biophys Acta       Date:  1998-04-28
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  3 in total

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Authors:  Steven L Robinette; Elaine Holmes; Jeremy K Nicholson; Marc E Dumas
Journal:  Genome Med       Date:  2012-04-30       Impact factor: 11.117

2.  Mutations in SELENBP1, encoding a novel human methanethiol oxidase, cause extraoral halitosis.

Authors:  Arjan Pol; G Herma Renkema; Albert Tangerman; Edwin G Winkel; Udo F Engelke; Arjan P M de Brouwer; Kent C Lloyd; Renee S Araiza; Lambert van den Heuvel; Heymut Omran; Heike Olbrich; Marijn Oude Elberink; Christian Gilissen; Richard J Rodenburg; Jörn Oliver Sass; K Otfried Schwab; Hendrik Schäfer; Hanka Venselaar; J Silvia Sequeira; Huub J M Op den Camp; Ron A Wevers
Journal:  Nat Genet       Date:  2017-12-18       Impact factor: 38.330

Review 3.  NMR Techniques in Metabolomic Studies: A Quick Overview on Examples of Utilization.

Authors:  Joanna Kruk; Marek Doskocz; Elżbieta Jodłowska; Anna Zacharzewska; Joanna Łakomiec; Kornelia Czaja; Jacek Kujawski
Journal:  Appl Magn Reson       Date:  2016-11-02       Impact factor: 0.831

  3 in total

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