Biochemical Journal

Research article

Autoproteolytic activation of human aspartylglucosaminidase

Jani SAARELA, Carita OINONEN, Anu JALANKO, Juha ROUVINEN, Leena PELTONEN

Abstract

Aspartylglucosaminidase (AGA) belongs to the N-terminal nucleophile (Ntn) hydrolase superfamily characterized by an N-terminal nucleophile as the catalytic residue. Three-dimensional structures of the Ntn hydrolases reveal a common folding pattern and equivalent stereochemistry at the active site. The activation of the precursor polypeptide occurs autocatalytically, and for some amidohydrolases of prokaryotes, the precursor structure is known and activation mechanisms are suggested. In humans, the deficient AGA activity results in a lysosomal storage disease, aspartylglucosaminuria (AGU) resulting in progressive neurodegeneration. Most of the disease-causing mutations lead to defective molecular maturation of AGA, and, to understand the structure–function relationship better, in the present study, we have analysed the effects of targeted amino acid substitutions on the activation process of human AGA. We have evaluated the effect of the previously published mutations and, in addition, nine novel mutations were generated. We could identify one novel amino acid, Gly258, with an important structural role on the autocatalytic activation of human AGA, and present the molecular mechanism for the autoproteolytic activation of the eukaryotic enzyme. Based on the results of the present study, and by comparing the available information on the activation of the Ntn-hydrolases, the autocatalytic processes of the prokaryotic and eukaryotic enzymes share common features. First, the critical nucleophile functions both as the catalytic and autocatalytic residue; secondly, the side chain of this nucleophile is oriented towards the scissile peptide bond; thirdly, conformational strain exists in the precursor at the cleavage site; finally, water molecules are utilized in the activation process.

  • activation mechanism
  • aspartylglucosaminidase
  • aspartylglucosaminuria
  • autocatalytic activation
  • Ntn-hydrolase
  • site-directed mutagenesis

Footnotes

  • 1 Present address: Department of Biochemistry, University of Kuopio, Savilahdentie 9, FIN-70211 Kuopio, Finland

  • Abbreviations used: AGA, aspartylglucosaminidase; AGU, aspartylglucosaminuria; ER, endoplasmic reticulum; Ntn, N-terminal nucleophile; rmsd, root mean square deviation; WT, wild-type.