Endopeptidase variations among different life‐cycle stages of African trypanosomes
- 1 January 1991
- journal article
- research article
- Published by Wiley in European Journal of Biochemistry
- Vol. 195 (1) , 183-190
- https://doi.org/10.1111/j.1432-1033.1991.tb15693.x
Abstract
Lysates of different life‐cycle stages of Trypanosoma congolense, Trypanosoma vivax and Trypanosoma brucei were analysed for endopeptidase activity, using reaction conditions which permitted a distinction to be made between lysosomal and non‐lysosomal activity [Lonsdale‐Eccles, J. D. & Grab, D. J. (1987) Eur. J. Biochem. 169, 467–475]. Hydrolysis of Z‐Arg‐Arg‐NHMec (Z = benzyloxycarbonyl, NHMec = 7‐amino‐4‐methylcoumaryl) and Z‐Gly‐Gly‐Arg‐NHMec occurred predominantly at alkaline pH and was observed in lysates of both insect and mammalian infective forms of T. brucei and T. congolense. Compared to their other life‐cycle stages, procyclic forms of T. brucei and epimastigote forms of T. congolense exhibited enhanced hydrolysis of these substrates. Low levels of hydrolysis of Z‐Arg‐Arg‐NHMec were observed in the bloodstream and epimastigote forms of T. vivax. The hydrolysis of Z‐Gly‐Gly‐Arg‐NHMec in each of the life‐cycle stages of T. vivax was generally below detectable levels.In lysates of T. congolense, proteolytic and Z‐Phe‐Arg‐NHMec‐hydrolytic activity in bloodstream forms > metacyclic > epimastigote > procyclic forms. In T. vivax Z‐Phe‐Arg‐NHMec‐hydrolytic activity differed slightly according to the origin of the parasite but, in general, followed the same pattern (i.e. bloodstream forms > epimastigote forms, with metacyclic forms usually intermediate between these two). In T. brucei, Z‐Phe‐Arg‐NHMec‐hydrolytic activity in bloodstream forms > procyclic forms. Upon differentiation of the long, slender bloodstream forms into short, stumpy forms the Z‐Phe‐Arg‐NHMec‐hydrolytic activity was elevated even further. Thus, during their life cycle, each of these African trypanosomes exhibits complex changes of endopeptidase activity, suggestive of an induction of lysosomal activity between the insect and mammalian forms.Keywords
This publication has 42 references indexed in Scilit:
- On the size of the active site in proteases. I. PapainPublished by Elsevier ,2005
- Substrate specificity and inhibitor sensitivity of a trypanosomatid alkaline peptidaseBiochimica et Biophysica Acta (BBA) - General Subjects, 1990
- Analysis of the proteinases of Trypanosoma bruceiJournal of General Microbiology, 1990
- Neutral proteases involved in the reinvasion of erythrocytes by Plasmodium merozoitesBiology of the Cell, 1988
- Purification of African Trypanosomes Can Cause Biochemical Changes in the Parasites1The Journal of Protozoology, 1987
- Trypanosoma vivax: Adaptation of Two East African Stocks to Laboratory Rodents1The Journal of Protozoology, 1987
- Alternative pathway activation of complement by African trypanosomes lacking a glycoprotein coatParasite Immunology, 1983
- Studies on the transmission of a West African stock of Trypanosoma vivax to rabbits, rats, mice and goats by Glossina morsitans morsitans and G. m. centralisInternational Journal for Parasitology, 1981
- New Culture Medium for Maintenance of Tsetse Tissues and Growth of Trypanosomatids*The Journal of Protozoology, 1977
- A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye bindingAnalytical Biochemistry, 1976