Back to Search Start Over

Function of Glycosomes in the Metabolism of Trypanosomatid Parasites and the Promise of Glycosomal Proteins as Drug Targets

Authors :
Ana J. Cáceres
Wilfredo Quiñones
Luisana Avilan
Juan Luis Concepción
Melisa Gualdrón-López
Paul A.M. Michels
Source :
Trypanosomatid Diseases: Molecular Routes to Drug Discovery
Publication Year :
2013
Publisher :
Wiley, 2013.

Abstract

Trypanosomatids have the unique feature of compartmentalizing the major part of the glycolytic pathway inside peroxisome-related organelles called glycosomes. However, these organelles also contain enzymes of several other important pathways involved in both catabolic and anabolic processes. The enzyme content and the metabolic role of glycosomes differ between trypanosomatid species and between their life cycle stages. Several of the glycosomal pathways have been shown to be important for the viability, pathogenicity, and/or virulence of different trypanosomatid parasites. Additionally, the correct compartmentalization of glycosomal enzymes inside the organelles appeared to be vital for these pathogens. Therefore, many of these enzymes, as well as the proteins involved in the translocation of metabolites across the glycosomal membrane and peroxins (PEXs), proteins responsible for the biogenesis of glycosomes, are candidate drug targets. Glycosomal enzymes and PEX proteins of Trypanosoma brucei, T. cruzi, and Leishmania spp. are being studied, and compounds that interfere with their functioning are being developed for use as lead drugs against the diseases caused by these parasites. Potent, selective inhibitors of several enzymes have been obtained that exert trypanocidal activity on parasites cultured in vitro and have no or only little effect on growth of human cells. In addition, some compounds showed anti-parasite activity in experimentally infected animals.

Details

Database :
OpenAIRE
Journal :
Trypanosomatid Diseases
Accession number :
edsair.doi...........2fb8be734fefe0fed08d04e638d14920
Full Text :
https://doi.org/10.1002/9783527670383.ch7