Hostname: page-component-586b7cd67f-t8hqh Total loading time: 0 Render date: 2024-11-22T23:42:12.507Z Has data issue: false hasContentIssue false

Detection of peptidases in Trypanosoma cruzi epimastigotes using chromogenic and fluorogenic substrates

Published online by Cambridge University Press:  06 April 2009

N. Healy
Affiliation:
Department of Biology, Imperial College of Science, Technology and Medicine, Prince Consort Road, London SW7 2BB, UK
S. Greig
Affiliation:
Department of Biology, Imperial College of Science, Technology and Medicine, Prince Consort Road, London SW7 2BB, UK
H. Enahoro
Affiliation:
Department of Biology, Imperial College of Science, Technology and Medicine, Prince Consort Road, London SW7 2BB, UK
H. Roberts
Affiliation:
Department of Biology, Imperial College of Science, Technology and Medicine, Prince Consort Road, London SW7 2BB, UK
L. Drake
Affiliation:
Department of Biology, Imperial College of Science, Technology and Medicine, Prince Consort Road, London SW7 2BB, UK
E. Shaw
Affiliation:
Friedrich Miescher-Institut, Basle, Switzerland
F. Ashall
Affiliation:
Department of Biology, Imperial College of Science, Technology and Medicine, Prince Consort Road, London SW7 2BB, UK

Summary

Detergent extracts of Trypanosoma cruzi epimastigotes catalysed the hydrolysis of a range of amino-acyl and peptidyl p-nitro-anilides and aminomethylcoumarins. At least three enzymes were detected that cleave Z–Phe–Arg–MCA. Two of these were optimally active at alkaline pH, the other at pH 4·0. Of the two enzymes with alkaline pH optima, one was a cysteine peptidase and was unable to cleave Bz–Arg–MCA readily, whilst the other cleaved Bz–Arg–MCA and was inhibited by diisopropyl fluorophosphate. The acidic enzyme was similar to cathespin L of other eukayrotes with respect to its pH profile, substrate-specificity and inhibitor-sensitivity. Evidence was presented that epimastigotes contain a cysteine-type dipeptidyl aminopeptidase, one or more aminopeptidases, and a serine peptidase that cleaves Boc–Ala–Ala–pNA. Digitonin solubilization of the activities from cells supports the hypothesis that the cathespin L-like enzyme and the dipeptidyl aminopeptidase are lysosomal, whilst the Bz–Arg–MCA hydrolase, the aminopeptidases and the Boc–Ala–Ala–pNA serine peptidase are cytosolic.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1992

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Ashall, F. (1990). Characterisation of an alkaline peptidase of Trypanosoma cruzi and other trypanosomatids. Molecular and Biochemical Parasitology 38, 7788.CrossRefGoogle ScholarPubMed
Ashall, F., Angliker, H. & Shaw, E. (1990 a). Lysis of trypanosomes by peptidyl fluoromethyl ketones. Biochemical and Biophysical Research Communications 170, 923–9.CrossRefGoogle ScholarPubMed
Ashall, F., Harris, D., Roberts, H., Healy, N. & Shaw, E. (1990 b). Substrate specificity and inhibitor sensitivity of a trypanosomatid alkaline peptidase. Biochimica et Biophysica Acta 1035, 293–9.CrossRefGoogle ScholarPubMed
Avila, J. L., Perez-Kepp, R. & Bretana, A. (1983). A minimal medium for the cultivation of infective Trypanosoma cruzi epimastigotes. Journal of General Microbiology 129, 285–91.Google ScholarPubMed
Barrett, A. J. & Kirschke, H. (1981). Cathespin B, cathepsin H and cathepsin L. Methods in Enzymology 80, 535–61.CrossRefGoogle Scholar
Bongertz, V. & Hungerer, K. D. (1978). Trypanosoma cruzi: isolation and characterisation of a protease. Experimental Parasitology 45, 818.CrossRefGoogle ScholarPubMed
Bontempi, E., Franke De Cazzulo, B. M., Ruiz, A. M. & Cazzulo, J. J. (1984). Purification and properties of an acidic protease from epimastigotes of Trypanosoma cruzi. Comparative Biochemistry and Physiology 77B, 599604.Google Scholar
Bontempi, E., Martinez, J. & Cazzulo, J. J. (1989). Subcellular localization of a cysteine proteinase from Trypanosoma cruzi. Molecular and Biochemical Parasitology 33, 43–8.CrossRefGoogle ScholarPubMed
Bradford, M. M. (1976). A rapid method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry 72, 248–54.CrossRefGoogle ScholarPubMed
Cazzulo, J. J., Cazzulo Franke, M. C., Martinez, J. & Franke De Cazzulo, B. M. (1990). Some kinetic properties of a cysteine proteinase (cruzipain) from Trypanosoma cruzi. Biochimica et Biophysica Acta 1037, 186–91.CrossRefGoogle ScholarPubMed
Davis, M. H. (1987). Hormonal regulation of dipeptidyl-aminopeptidase I activity in cultured human fibroblasts. Archives of Biochemistry and Biophysics 254, 498503.CrossRefGoogle ScholarPubMed
Erlanger, B. F., Kokowsky, N. & Cohen, W. (1961). The preparation and properties of two new chromogenic substrates of trypsin. Archives of Biochemistry and Biophysics 95, 271–8.CrossRefGoogle ScholarPubMed
Etges, R., Bouvier, J. & Bordier, C. (1986). The major surface protein of Leishmania promastigotes is a protease. Journal of Biological Chemistry 261, 9098–101.CrossRefGoogle ScholarPubMed
Greig, S. & Ashall, F. (1990). Electrophoretic characterisation of Trypanosoma cruzi peptidases. Molecular and Biochemical Parasitology 39, 31–8.CrossRefGoogle ScholarPubMed
Hui, K.-S. (1988). A novel dipeptidyl aminopeptidase in rat brain membranes. Journal of Biological Chemistry 263, 6613–18.CrossRefGoogle ScholarPubMed
Itow, & Camargo, E. P. (1977). Proteolytic activities in cell extracts of Trypanosoma cruzi. Journal of Protozoology 24, 591–5.CrossRefGoogle ScholarPubMed
Kam, C. M., Fujikawa, K. & Powers, J. C. (1988). Mechanism-based isocoumarin inhibitors for trypsin and blood coagulation serine proteases: new anticoagulants. Biochemistry 27, 2547–57.CrossRefGoogle ScholarPubMed
Kirshke, H., Wikstrom, P. & Shaw, E. (1988). Active center differences between cathepsins L and B: the S1 binding region. FEBS Letters 228, 128–30.CrossRefGoogle Scholar
Lonsdale-Eccles, J. D. & Grab, D. J. (1987). Lysosomal and non-lysosomal peptidyl hydrolases of the bloodstream forms of Trypanosoma brucei brucei. European Journal of Biochemistry 169, 467–75.CrossRefGoogle ScholarPubMed
Piras, M. M., Henriquez, D. & Piras, R. (1985). The effect of proteolytic enzymes and protease inhibitors on the interaction Trypanosoma cruzi-fibroblasts. Molecular and Biochemical Parasitology 14, 151–63.CrossRefGoogle ScholarPubMed
Rangel, H. A., Araujo, P. M. F., Repka, D. & Costa, M. G. (1981). Trypanosoma cruzi: isolation and characterisation of a proteinase. Experimental Parasitology 52, 199209.CrossRefGoogle ScholarPubMed
Rauber, P., Angliker, H., Walker, B. & Shaw, E. (1986). The synthesis of peptidylfluoromethanes and their properties as inhibitors of serine proteinases and cysteine proteinases. The Biochemical Journal 239, 633–40.CrossRefGoogle ScholarPubMed
Schechter, I. & Berger, A. (1967). On the size of the active site in proteases. I. Papain. Biochemical and Biophysical Research Communications 27, 157–62.CrossRefGoogle ScholarPubMed
Silva, L. H. P. & Nussenzweig, V. (1963). Sobre uma cepa de Trypanosoma cruzi altamente virulenta para o camundongo branco. Folia Clinica Biologica 20, 191203.Google Scholar