A fluorimetric enzyme assay for the diagnosis of Sanfilippo disease C (MPS III C)

J Inherit Metab Dis. 1993;16(2):465-72. doi: 10.1007/BF00710299.

Abstract

Both the alpha- and beta-anomers of 4-methylumbelliferyl-D-glucosaminide were synthesized and shown to be substrates for the lysosomal acetyl-CoA:glucosaminide N-acetyltransferase. Using the beta-anomer, fibroblasts and leukocytes from 11 different Sanfilippo C patients showed < 1% of mean normal N-acetyltransferase activity. Heterozygotes showed intermediate activities. The enzymatic liberation of the fluorochrome from 4-methylumbelliferyl-beta-D-glucosaminide requires the sequential action of the N-acetyltransferase and beta-hexosaminidase. Normal beta-hexosaminidase activity caused complete hydrolysis of the reaction intermediate 4-methylumbelliferyl-beta-D-N-acetylglucosaminide formed by the N-acetyltransferase. In cell extracts with a beta-hexosaminidase deficiency, however, a second incubation in the presence of excess beta-hexosaminidase is needed to avoid underestimation of the N-acetyltransferase activity.

MeSH terms

  • Acetyltransferases / deficiency
  • Acetyltransferases / metabolism*
  • Cells, Cultured
  • Fibroblasts / enzymology
  • Fluorometry
  • Heterozygote
  • Humans
  • Hymecromone / analogs & derivatives
  • Hymecromone / metabolism
  • Leukocytes / enzymology
  • Mucopolysaccharidosis III / diagnosis*
  • Mucopolysaccharidosis III / enzymology
  • Reference Values

Substances

  • 4-methylumbelliferyl-beta-glucosaminide
  • Hymecromone
  • Acetyltransferases
  • glucosamine acetyltransferase