Biochemical and structural insights into an allelic variant causing the lysosomal storage disorder - aspartylglucosaminuria

FEBS Lett. 2018 Aug;592(15):2550-2561. doi: 10.1002/1873-3468.13190. Epub 2018 Jul 23.

Abstract

Aspartylglucosaminuria (AGU) is a lysosomal storage disorder caused by defects of the hydrolase glycosylasparaginase (GA). Previously, we showed that a Canadian AGU mutation disrupts an obligatory intramolecular autoprocessing with the enzyme trapped as an inactive precursor. Here, we report biochemical and structural characterizations of a model enzyme corresponding to a Finnish AGU allele, the T234I variant. Unlike the Canadian counterpart, the Finnish variant is capable of a slow autoprocessing to generate detectible hydrolyzation activity of the natural substrate of GA. We have determined a 1.6 Å-resolution structure of the Finnish AGU model and built an enzyme-substrate complex to provide a structural basis for analyzing the negative effects of the point mutation on KM and kcat of the mature enzyme.

Enzyme: Glycosylasparaginase or aspartylglucosaminidase, EC3.5.1.26.

Keywords: aspartylglucosaminuria; autoprocessing; autoproteolysis; crystal structure; glycosylasparaginase; kinetic characterization.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Alleles
  • Amino Acid Sequence
  • Amino Acid Substitution / genetics
  • Aspartylglucosaminuria / enzymology
  • Aspartylglucosaminuria / genetics*
  • Aspartylglucosylaminase / chemistry*
  • Aspartylglucosylaminase / genetics*
  • Aspartylglucosylaminase / metabolism
  • Crystallography, X-Ray
  • Finland
  • Homeostasis / genetics
  • Humans
  • Lysosomal Storage Diseases / genetics
  • Models, Molecular
  • Point Mutation*
  • Protein Structure, Secondary
  • Proteolysis

Substances

  • Aspartylglucosylaminase