Relaxed specificity of endoproteinase Asp-N: this enzyme cleaves at peptide bonds N-terminal to glutamate as well as aspartate and cysteic acid residues

Biochem Int. 1990 Nov;22(3):561-6.

Abstract

Asp-N, an endoproteinase specific for cleavage of protein or polypeptide bonds N-terminal to aspartate or cysteic acid residues, has been shown to possess a similar affinity for certain glutamate residues. Of 18 glutamate residues present in 2 cyanogen bromide fragments of apolipoprotein A-I, 5 residues were cleaved at rates comparable to that of cleavage at the 12 internal aspartate residues present in these polypeptides (all of which were cleaved). Cleavage of these 5 glutamate residues was obtained under standard enzyme digestion conditions, and the identities of all peptides obtained by Asp-N digestion were determined by amino acid sequencing of peaks obtained from reversed-phase high performance liquid chromatography.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Amino Acids / analysis
  • Apolipoprotein A-I
  • Apolipoproteins A / metabolism
  • Aspartic Acid
  • Chromatography, High Pressure Liquid
  • Cysteic Acid
  • Endopeptidases / metabolism*
  • Glutamates
  • Glutamic Acid
  • Humans
  • Metalloendopeptidases
  • Molecular Sequence Data
  • Peptide Fragments / metabolism*
  • Substrate Specificity

Substances

  • Amino Acids
  • Apolipoprotein A-I
  • Apolipoproteins A
  • Glutamates
  • Peptide Fragments
  • Aspartic Acid
  • Glutamic Acid
  • Cysteic Acid
  • Endopeptidases
  • Metalloendopeptidases
  • endoproteinase Asp-N