A FLUOROMETRIC ENZYME ASSAY FOR THE DIAGNOSIS OF SANFILIPPO DISEASE TYPE-D (MPS IIID)

被引:37
作者
HE, W
VOZNYI, YV
BOER, AM
VANDIGGELEN, OP
KLEIJER, WJ
机构
[1] ERASMUS UNIV ROTTERDAM,DEPT CLIN GENET,3000 DR ROTTERDAM,NETHERLANDS
[2] ACAD SCI ARMENIAN REPUBL,INST BIOCHEM,YEREVAN,ARMENIA
关键词
D O I
10.1007/BF00711508
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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-acetylgluco-saminide 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.
引用
收藏
页码:935 / 941
页数:7
相关论文
共 15 条
[1]  
BASNER R, 1979, J BIOL CHEM, V254, P1151
[2]   CLINICAL HETEROGENEITY IN SANFILIPPO DISEASE (MUCOPOLYSACCHARIDOSIS-III) TYPE-D - PRESENTATION OF 2 NEW CASES [J].
COPPA, GV ;
GIORGI, PL ;
FELICI, L ;
GABRIELLI, O ;
DONTI, E ;
BERNASCONI, S ;
KRESSE, H ;
PASCHKE, E ;
MASTROPAOLO, C .
EUROPEAN JOURNAL OF PEDIATRICS, 1983, 140 (02) :130-133
[3]   HUMAN GLUCOSAMINE-6-SULFATASE DEFICIENCY - DIAGNOSTIC ENZYMOLOGY TOWARDS HEPARIN-DERIVED TRISACCHARIDE SUBSTRATES [J].
FREEMAN, C ;
HOPWOOD, JJ .
BIOCHEMICAL JOURNAL, 1992, 282 :605-614
[4]   SANFILIPPO TYPE-D DISEASE - CLINICAL FINDINGS IN 2 PATIENTS WITH A NEW VARIANT OF MUCOPOLYSACCHARIDOSIS-III [J].
GATTI, R ;
BORRONE, C ;
DEVIRGILIS, S ;
SANNA, G ;
CAO, A ;
VONFIGURA, K ;
KRESSE, H ;
PASCHKE, E ;
DURAND, P .
EUROPEAN JOURNAL OF PEDIATRICS, 1982, 138 (02) :168-171
[5]   SANFILIPPO SYNDROME TYPE-D [J].
KAPLAN, P ;
WOLFE, LS .
JOURNAL OF PEDIATRICS, 1987, 110 (02) :267-271
[6]   SANFILIPPO DISEASE TYPE-D - DEFICIENCY OF N-ACETYLGLUCOSAMINE-6-SULFATE SULFATASE REQUIRED FOR HEPARAN-SULFATE DEGRADATION [J].
KRESSE, H ;
PASCHKE, E ;
VONFIGURA, K ;
GILBERG, W ;
FUCHS, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (11) :6822-6826
[7]   KERATAN AND HEPARAN SULFATURIA - A MUCOPOLYSACCHARIDOSIS WITH AN ENZYME DEFECT NOT PREVIOUSLY IDENTIFIED [J].
MATALON, R ;
WAPPNER, R ;
DEANCHING, M ;
BRANDT, IK ;
HORWITZ, A .
JOURNAL OF INHERITED METABOLIC DISEASE, 1982, 5 :57-58
[8]  
NAWAKOWSKI RW, 1989, PEDIATR RES, V26, P462
[9]  
Neufeld EF, 1989, METABOLIC BASIS INHE, P1565
[10]   SANFILIPPO SYNDROME TYPE-D IN 2 ADOLESCENT SISTERS [J].
SICILIANO, L ;
FIUMARA, A ;
PAVONE, L ;
FREEMAN, C ;
ROBERTSON, D ;
MORRIS, CP ;
HOPWOOD, JJ ;
DINATALE, P ;
MUSUMECI, S ;
HORWITZ, AL .
JOURNAL OF MEDICAL GENETICS, 1991, 28 (06) :402-405