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Expression and functional characterization of human mutant sulfamidase in insect cells.

Authors
  • Montfort, Magda
  • Garrido, Elena
  • Hopwood, John J
  • Grinberg, Daniel
  • Chabás, Amparo
  • Vilageliu, Lluïsa
Type
Published Article
Journal
Molecular genetics and metabolism
Publication Date
Nov 01, 2004
Volume
83
Issue
3
Pages
246–251
Identifiers
PMID: 15542396
Source
Medline
License
Unknown

Abstract

Mucopolysaccharidosis IIIA (MPS IIIA; Sanfilippo syndrome) is an autosomal recessive lysosomal disorder caused by the deficiency of sulfamidase (EC 3.10.1.1), required for the degradation of the mucopolysaccharide heparan sulfate. The molecular defects of 26 unrelated Spanish MPS IIIA patients were recently reported by our group. Here we describe the heterologous expression, using a baculovirus system, of the cDNAs corresponding to eight out of the 14 mutant alleles present in this patient group and the characterization of the corresponding mutant enzymes. In particular, we expressed the following alleles: p.S66W, p.R74H, p.Q85R, p.R206P, p.L386R, p.R433W, p.R433Q, and c.1079delC (previously named as c.1091delC), and the two variants of the polymorphism p.R456H. The expression of the mutant alleles and the characterization of the corresponding enzymes revealed that their activity was severely compromised. Only mutations p.S66W and p.R206P retained low levels of residual activity. However, Western blot analysis showed in all cases the presence of the expected two forms of the sulfamidase, the precursor and the mature proteins, indicating a normal processing of the mutant enzyme.

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