Inhibition of cruzipain, the major cysteine proteinase of the protozoan parasite, Trypanosoma cruzi, by proteinase inhibitors of the cystatin superfamily

Cruzipain, the major cysteine proteinase from Trypanosoma cruzi epimastigotes, purified to a sequentially pure form, exists in multiple forms with pI values between 3.7 and 5.1, and an apparent molecular mass of 41 kDa. The enzyme is stable between pH 4.5–9.5. Cruzipain was found to be rapidly and t...

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Published inFEBS letters Vol. 370; no. 1; pp. 101 - 104
Main Authors Stoka, Veronika, Nycander, Maria, Lenarčič, Brigita, Labriola, Carlos, Cazzulo, Juan José, Björk, Ingemar, Turk, Vito
Format Journal Article
LanguageEnglish
Published England Elsevier B.V 14.08.1995
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Summary:Cruzipain, the major cysteine proteinase from Trypanosoma cruzi epimastigotes, purified to a sequentially pure form, exists in multiple forms with pI values between 3.7 and 5.1, and an apparent molecular mass of 41 kDa. The enzyme is stable between pH 4.5–9.5. Cruzipain was found to be rapidly and tightly inhibited by various protein inhibitors of the cystatin superfamily ( k ass = 1.7–79 × 10 6M −1s −1, K d = 1.4–72 pM). These results suggest a possible defensive role for the host's cystatins after parasite infection, and may be of use for the design of new therapeutic drugs.
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ISSN:0014-5793
1873-3468
DOI:10.1016/0014-5793(95)00798-E