Maturation processing and characterization of streptopain

J Biol Chem. 2003 May 9;278(19):17336-43. doi: 10.1074/jbc.M209038200. Epub 2003 Mar 5.

Abstract

Streptopain is a cysteine protease expressed by Streptococcus pyogenes. To study the maturation mechanism of streptopain, wild-type and Q186N, C192S, H340R, N356D and W357A mutant proteins were expressed in Escherichia coli and purified to homogeneity. Proteolytic analyses showed that the maturation of prostreptococcal pyrogenic exotoxin B zymogen (pro-SPE B) involves eight intermediates with a combination of cis- and trans-processing. Based on the sequences of these intermediates, the substrate specificity of streptopain favors a hydrophobic residue at the P2 site. The relative autocatalytic rates of these mutants exhibited the order Q186N > W357A > N356D, C192S, H340R. Interestingly, the N356D mutant containing protease activity could not be converted into the 28-kDa form by autoprocessing. This observation suggested that Asn(356) might involve the cis-processing of the propeptide. In addition, the maturation rates of pro-SPE B with trypsin and plasmin were 10- and 60-fold slower than that with active mature streptopain. These findings indicate that active mature streptopain likely plays the most important role in the maturation of pro-SPE B under physiological conditions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Cysteine Endopeptidases / metabolism*
  • Escherichia coli
  • Fibrinolysin
  • Molecular Sequence Data
  • Protein Folding
  • Protein Processing, Post-Translational*
  • Recombinant Proteins / metabolism
  • Streptococcus pyogenes / enzymology*
  • Trypsin

Substances

  • Recombinant Proteins
  • Trypsin
  • Fibrinolysin
  • Cysteine Endopeptidases
  • streptopain