http://repositorio.unb.br/handle/10482/47962
Arquivo | Descrição | Tamanho | Formato | |
---|---|---|---|---|
ARTIGO_ProlylOligopeptidaseLeishmania.pdf | 1,68 MB | Adobe PDF | Visualizar/Abrir |
Título: | Prolyl oligopeptidase from Leishmania infantum : biochemical characterization and involvement in macrophage infection |
Autor(es): | Silva, Camila Lasse Azevedo, Clênia Santos Araújo, Carla Nunes de Motta, Flávia Nader da Silva Andrade, Milene Aparecida Rocha, Amanda Pereira Sampaio, Iracyara Charneau, Sébastien Gèze, Marc Grellier, Phillippe Santana, Jaime Martins de Bastos, Izabela Marques Dourado |
Afiliação do autor: | University of Brasília, Department of Cell Biology, Pathogen-Host Interface Laboratory University of Brasília, Department of Cell Biology, Pathogen-Host Interface Laboratory UMR 7245 MCAM, Musèum National d’Histoire Naturelle, Centre National de la Recherche Scientifique, Paris, France University of Brasília, Department of Cell Biology, Pathogen-Host Interface Laboratory University of Brasília, Faculty of Ceilandia University of Brasília, Department of Cell Biology, Pathogen-Host Interface Laboratory University of Brasília, Faculty of Ceilandia University of Brasília, Department of Cell Biology, Pathogen-Host Interface Laboratory UMR 7245 MCAM, Musèum National d’Histoire Naturelle, Centre National de la Recherche Scientifique, Paris, France University of Brasília, Department of Cell Biology, Pathogen-Host Interface Laboratory University of Brasília, Department of Cell Biology, Pathogen-Host Interface Laboratory University of Brasília, Department of Cell Biology, Laboratory of Protein Chemistry and Biochemistry UMR 7245 MCAM, Musèum National d’Histoire Naturelle, Centre National de la Recherche Scientifique, Paris, France CeMIM, Musèum National d’Histoire Naturelle, Paris, France UMR 7245 MCAM, Musèum National d’Histoire Naturelle, Centre National de la Recherche Scientifique, Paris, France University of Brasília, Department of Cell Biology, Pathogen-Host Interface Laboratory University of Brasília, Department of Cell Biology, Pathogen-Host Interface Laboratory |
Assunto: | Leishmania infantum Prolil oligopetidase |
Data de publicação: | 2020 |
Editora: | Frontiers |
Referência: | LASSE, CAMILA et al. Prolyl oligopeptidase from Leishmania infantum: biochemical characterization and involvement in macrophage infection. Frontiers in Microbiology, [S. l.], v. 11, 2020. DOI: https://doi.org/10.3389/fmicb.2020.01060. Disponível em: https://www.frontiersin.org/journals/microbiology/articles/10.3389/fmicb.2020.01060/full. |
Abstract: | Leishmania infantum is a flagellated protozoan and one of the main causative agents of visceral leishmaniasis. This disease usually affects the human reticuloendothelial system, can cause death and available therapies may lead to serious side effects. Since it is a neglected tropical disease, the incentives for the development of new drugs are insufficient. It is important to know Leishmania virulence factors that contribute most to the disease in order to develop drugs. In the present work, we have produced L. infantum prolyl oligopeptidase (rPOPLi) in Escherichia coli, and investigated its biochemical properties as well as the effect of POP inhibitors on its enzymatic activity and on the inhibition of the macrophage infection by L. infantum. The optimal activity occurred at pH 7.5 and 37°C in the presence of DTT, the latter increased rPOPLi catalytic efficiency 5-fold on the substrate N-Suc-Gly-Pro-Leu-Gly-Pro-AMC. The enzyme was inhibited by TPCK, TLCK and by two POP specific inhibitors, Z-Pro-prolinal (ZPP, IC50 4.2 nM) and S17092 (IC50 3.5 nM). Besides being a cytoplasmic enzyme, POPLi is also found in punctuate structures within the parasite cytoplasm or associated with the parasite plasma membrane in amastigotes and promastigotes, respectively. Interestingly, S17092 and ZPP prevented parasite invasion in murine macrophages, supporting the involvement of POPLi in the invasive process of L. infantum. These data suggest POPLi as a virulence factor that offers potential as a target for designing new antileishmanial drugs. |
Unidade Acadêmica: | Instituto de Ciências Biológicas (IB) Departamento de Biologia Celular (IB CEL) Faculdade UnB Ceilândia (FCE) Colegiado de Bases Biológicas e da Saúde (FCE-BASES) |
DOI: | https://doi.org/10.3389/fmicb.2020.01060 |
Aparece nas coleções: | Artigos publicados em periódicos e afins |
Os itens no repositório estão protegidos por copyright, com todos os direitos reservados, salvo quando é indicado o contrário.