Literature DB >> 8183833

Prenatal diagnosis of Sanfilippo disease type C using a simple fluorometric enzyme assay.

W He1, J G Huijmans, G C Geilen, E A Karpova, T V Dudukina, J Zaremba, O P Van Diggelen, W J Kleijer.   

Abstract

A new fluorogenic substrate, 4-methylumbelliferyl beta-D-glucosaminide, was used for the assay of acetyl CoA:glucosaminide N-acetyltransferase in chorionic villi, cultured villus cells, and amniocytes. Optimal conditions for the assay and the ranges of enzyme activity were established for the various types of fetal cells. This simple fluorometric assay provides a reliable method for early prenatal diagnosis of Sanfilippo disease type C which is more convenient than current methods using radiolabelled substrates. The method was applied to amniotic fluid cells and fetal fibroblasts from an at-risk pregnancy in which an affected fetus was diagnosed by two-dimensional electrophoresis of glycosaminoglycans in the amniotic fluid.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 8183833     DOI: 10.1002/pd.1970140104

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  8 in total

1.  New substrates and enzyme assays for the detection of mucopolysaccharidosis III (Sanfilippo Syndrome) types A, B, C, and D by tandem mass spectrometry.

Authors:  Brian J Wolfe; Farideh Ghomashchi; Tim Kim; Cynthia A Abam; Martin Sadilek; Rhona Jack; Jerry N Thompson; C Ronald Scott; Michael H Gelb; Frantisek Turecek
Journal:  Bioconjug Chem       Date:  2012-03-09       Impact factor: 4.774

2.  Sialic acid catabolism by N-acetylneuraminate pyruvate lyase is essential for muscle function.

Authors:  Xiao-Yan Wen; Maja Tarailo-Graovac; Koroboshka Brand-Arzamendi; Anke Willems; Bojana Rakic; Karin Huijben; Afitz Da Silva; Xuefang Pan; Suzan El-Rass; Robin Ng; Katheryn Selby; Anju Mary Philip; Junghwa Yun; X Cynthia Ye; Colin J Ross; Anna M Lehman; Fokje Zijlstra; N Abu Bakar; Britt Drögemöller; Jacqueline Moreland; Wyeth W Wasserman; Hilary Vallance; Monique van Scherpenzeel; Farhad Karbassi; Martin Hoskings; Udo Engelke; Arjan de Brouwer; Ron A Wevers; Alexey V Pshezhetsky; Clara Dm van Karnebeek; Dirk J Lefeber
Journal:  JCI Insight       Date:  2018-12-20

3.  The microcell-mediated transfer of human chromosome 8 restores the deficient N-acetylytransferase activity in skin fibroblasts of Mucopolysaccharidosis type IIIC patients.

Authors:  Volkan Seyrantepe; Frédérique Tihy; Alexey V Pshezhetsky
Journal:  Hum Genet       Date:  2006-06-17       Impact factor: 4.132

4.  Analysis of the biogenesis of heparan sulfate acetyl-CoA:alpha-glucosaminide N-acetyltransferase provides insights into the mechanism underlying its complete deficiency in mucopolysaccharidosis IIIC.

Authors:  Stéphanie Durand; Matthew Feldhammer; Eric Bonneil; Pierre Thibault; Alexey V Pshezhetsky
Journal:  J Biol Chem       Date:  2010-07-22       Impact factor: 5.157

Review 5.  Sanfilippo syndrome: a mini-review.

Authors:  M J Valstar; G J G Ruijter; O P van Diggelen; B J Poorthuis; F A Wijburg
Journal:  J Inherit Metab Dis       Date:  2008-04-04       Impact factor: 4.982

6.  Activatable Optical Probes for the Detection of Enzymes.

Authors:  Christopher R Drake; David C Miller; Ella F Jones
Journal:  Curr Org Synth       Date:  2011-08       Impact factor: 1.975

7.  Characterization of the biosynthesis, processing and kinetic mechanism of action of the enzyme deficient in mucopolysaccharidosis IIIC.

Authors:  Xiaolian Fan; Ilona Tkachyova; Ankit Sinha; Brigitte Rigat; Don Mahuran
Journal:  PLoS One       Date:  2011-09-21       Impact factor: 3.240

8.  Protein misfolding as an underlying molecular defect in mucopolysaccharidosis III type C.

Authors:  Matthew Feldhammer; Stéphanie Durand; Alexey V Pshezhetsky
Journal:  PLoS One       Date:  2009-10-13       Impact factor: 3.240

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.