منابع مشابه
Cysteine Protease Inhibitors and Parasitic Diseases
ABBREVIATIONS BBB: Blood brain barrier, CP: Cysteine protease, CPI: cysteine protease inhibitor, E-64: Epoxid compound: Clonazepam©, E/S: Excretory-secretory, FP2: Falcipain-2HDAC: Histone deacetylases, IFN: Interferon, LC: Lactacystin, NO: Nitrous oxide, PCD: Programmed cell death, PMN: Polymorphonuclear neutrophil granulocytes, PMSF: Phenyl-methylsulfonyl fluoride, PVS: Polyvenyl sulfone, SBT...
متن کاملStudies of Inhibitory Mechanisms of Propeptide-Like Cysteine Protease Inhibitors
Mouse cytotoxic T-lymphocyte antigen-2α (CTLA-2α), Drosophila CTLA-2-like protein (crammer), and Bombyx cysteine protease inhibitor (BCPI) belong to a novel family of cysteine protease inhibitors (I29). Their inhibitory mechanisms were studied comparatively. CTLA-2α contains a cysteine residue (C75), which is essential for its inhibitory potency. The CTLA-2α monomer was converted to a disulfide...
متن کاملAntimalarial activities of novel synthetic cysteine protease inhibitors.
Among promising new targets for antimalarial chemotherapy are the cysteine protease hemoglobinases falcipain-2 and falcipain-3. We evaluated the activities of synthetic peptidyl aldehyde and alpha-ketoamide cysteine protease inhibitors against these proteases, against cultured Plasmodium falciparum parasites, and in a murine malaria model. Optimized compounds inhibited falcipain-2 and falcipain...
متن کاملMedical significance of cysteine protease inhibitors in mammalian secretory fluids.
New cysteine protease inhibitors in human tears and milk and their medical significance are reviewed in this paper. As protective components against bacterial infection in the eyes, we detected four kinds of anti-bacterial proteins in normal human tears including lysozyme and three kinds of cysteine protease inhibitors. Using our reverse zymography of normal tears, three kinds of cysteine prote...
متن کاملCysteine Protease Inhibitors Cure an Experimental Trypanosoma cruzi Infection
Trypanosoma cruzi is the causative agent of Chagas' disease. The major protease, cruzain, is a target for the development of new chemotherapy. We report the first successful treatment of an animal model of Chagas' disease with inhibitors designed to inactivate cruzain. Treatment with fluoromethyl ketone-derivatized pseudopeptides rescued mice from lethal infection. The optimal pseudopeptide sca...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Cellular and Molecular Life Sciences
سال: 2005
ISSN: 1420-682X,1420-9071
DOI: 10.1007/s00018-004-4445-9