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A fluorimetric enzyme assay for the diagnosis of Sanfilippo disease type D (MPS IIID).

Authors :
He W
Voznyi YaV
Boer AM
Kleijer WJ
van Diggelen OP
Source :
Journal of inherited metabolic disease [J Inherit Metab Dis] 1993; Vol. 16 (6), pp. 935-41.
Publication Year :
1993

Abstract

4-Methylumbelliferyl-alpha-N-acetylglucosamine 6-sulphate was synthesized and shown to be a substrate for the lysosomal N-acetylglucosamine-6-sulphate sulphatase (GlcNAc-6S sulphatase). Fibroblasts and leukocytes from 3 different Sanfilippo D patients showed < 1% of mean normal GlcNAc-6S sulphatase activity. The enzymatic liberation of the fluorochrome from 4-methyl-umbelliferyl-alpha-N-acetylglucosamine 6-sulphate requires the sequential action of the GlcNAc-6S sulphatase and alpha-N-acetylglucosaminidase. A normal level of alpha-N-acetylglucosaminidase activity was insufficient to complete the hydrolysis of the reaction intermediate 4-methylumbelliferyl-alpha-N-acetylglucosaminide formed by the GlcNAc-6S sulphatase. A second incubation in the presence of excess alpha-N-acetylglucosaminidase is needed to avoid underestimation of the GlcNAc-6S sulphatase activity.

Details

Language :
English
ISSN :
0141-8955
Volume :
16
Issue :
6
Database :
MEDLINE
Journal :
Journal of inherited metabolic disease
Publication Type :
Academic Journal
Accession number :
8127069
Full Text :
https://doi.org/10.1007/BF00711508