Properties of alpha-L-iduronidase in cultured skin fibroblasts from alpha-L-iduronidase-deficient patients

Hum Genet. 1984;65(3):268-72. doi: 10.1007/BF00286515.

Abstract

On DEAE cellulose column chromatography, alpha-L-iduronidase in cultured skin fibroblasts was resolved into two distinct components, forms A and B. They had similar Km values for 4-methylumbelliferyl-alpha-L-iduronide, but differed in pH optima and thermal stability. Form B was more heat-stable than form A. Residual alpha-L-iduronidase activity in Hurler fibroblasts was heat-stable, while that in Scheie fibroblasts was heat-labile, and moreover, that in Hurler-Scheie compound fibroblasts lay intermediate between Hurler and Scheie syndromes. These findings demonstrated that Hurler syndrome, Scheie syndrome and Hurler-Scheie compound were enzymatically distinguishable.

MeSH terms

  • Cells, Cultured
  • Chromatography, DEAE-Cellulose
  • Clinical Enzyme Tests*
  • Diagnosis, Differential
  • Female
  • Fibroblasts / enzymology
  • Glycoside Hydrolases / deficiency*
  • Heterozygote
  • Hot Temperature
  • Humans
  • Iduronidase / analysis
  • Iduronidase / deficiency*
  • Iduronidase / genetics
  • Kinetics
  • Male
  • Mucopolysaccharidoses / diagnosis*
  • Mucopolysaccharidosis I / diagnosis*
  • Mucopolysaccharidosis I / genetics
  • Skin / cytology

Substances

  • Glycoside Hydrolases
  • Iduronidase