| Texto completo | |
| Autor(es): |
Farias, Shirley L.
;
Gazarini, Marcos L.
;
Melo, Robson L.
;
Hirata, Izaura Y.
;
Juliano, Maria A.
;
Juliano, Luiz
[6]
;
Garcia, Célia R. S.
Número total de Autores: 7
|
| Tipo de documento: | Artigo Científico |
| Fonte: | Molecular and Biochemical Parasitology; v. 141, n. 1, p. 71-79, May 2005. |
| Área do conhecimento: | Ciências Biológicas - Biofísica |
| Assunto(s): | Doenças parasitárias Malária Melatonina Cálcio Enzimas Cisteína endopeptidases Calpaína |
| Resumo | |
Bloodstage malaria parasites require proteolytic activity for key processes as invasion, hemoglobin degradation and merozoite escape from red blood cells (RBCs). We investigated by confocal microscopy the presence of cysteine-protease activity elicited by calcium stimulus in Plasmodium chabaudi and Plasmodium falciparum in free trophozoites or for the later parasite within RBC using fluorescence resonance energy transfer (FRET) peptides. Peptide probes access, to either free or intraerythrocytic parasites, was also tested by selecting a range of fluorescent peptides (653-3146 Da molecular mass) labeled with Abz or FITC. In the present work we show that Ca2+ stimulus elicited by treatment with either melatonin, thapsigargin, ionomicin or nigericin, promotes an increase of substrate hydrolysis, which was blocked by the specific cysteine-protease inhibitor E-64 and the intracellular Ca2+ chelator, BAPTA. When parasites were treated with cytoplasmic Ca2+ releasing compounds, a cysteine-protease was labeled in the parasite cytoplasm by the fluorescent specific irreversible inhibitor, Ethyl-Eps-Leu-Tyr-Cap-Lys(Abz)-NH2, where Ethyl-Eps is Ethyl-(2S,3S)-oxirane-2,3-dicarboxylate. In summary, we demonstrate that P. chabaudi and P. falciparum have a cytoplasmic dependent cysteine-protease activity elicited by Ca2+. (AU) | |
| Processo FAPESP: | 02/06194-7 - Bases moleculares da transdução de sinal do ciclo celular de parasitas de malária |
| Beneficiário: | Célia Regina da Silva Garcia |
| Modalidade de apoio: | Auxílio à Pesquisa - Temático |
| Processo FAPESP: | 03/09994-7 - Substratos e inibidores peptídicos para enzimas proteolíticas |
| Beneficiário: | Luiz Juliano Neto |
| Modalidade de apoio: | Auxílio à Pesquisa - Programa PRONEX - Temático |