Purification and partial characterization of a cysteine proteinase from Trypanosoma rangeli

FEMS Microbiol Lett. 1995 Jun 15;129(2-3):143-8. doi: 10.1111/j.1574-6968.1995.tb07571.x.

Abstract

Epimastigotes of the American Trypanosome Trypanosoma rangeli contain a very low cysteine proteinase (CP) activity. The enzyme was purified to homogeneity by affinity chromatography on ConA-Sepharose and Cystatin-Sepharose. This CP had a similar apparent molecular mass and an identical N-terminal sequence (15 amino acids) as compared with cruzipain from Trypanosoma cruzi; cross-reacted immunologically with the latter enzyme, it was inhibited by E-64 and TLCK, but not by PMSF, o-phenanthroline or Pepstatin, and was able to use the same substrates, although with different order of effectiveness and optimum pH.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Cysteine Endopeptidases / chemistry
  • Cysteine Endopeptidases / isolation & purification*
  • Enzyme Activation
  • Molecular Sequence Data
  • Substrate Specificity
  • Trypanosoma / enzymology*

Substances

  • Cysteine Endopeptidases