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Glycolysis in the African Trypanosome: Targeting Enzymes and Their Subcellular Compartments for Therapeutic Development
Author(s) -
April F. Coley,
Heidi Dodson,
Meredith T. Morris,
James C. Morris
Publication year - 2011
Publication title -
molecular biology international
Language(s) - English
Resource type - Journals
eISSN - 2090-2190
pISSN - 2090-2182
DOI - 10.4061/2011/123702
Subject(s) - trypanosoma brucei , african trypanosomiasis , glycolysis , host (biology) , tsetse fly , biology , vector (molecular biology) , computational biology , subcellular localization , trypanosoma , microbiology and biotechnology , carbohydrate metabolism , enzyme , metabolic pathway , trypanosomiasis , biochemistry , virology , genetics , gene , ecology , cytoplasm , recombinant dna
Subspecies of the African trypanosome, Trypanosoma brucei , which cause human African trypanosomiasis, are transmitted by the tsetse fly, with transmission-essential lifecycle stages occurring in both the insect vector and human host. During infection of the human host, the parasite is limited to using glycolysis of host sugar for ATP production. This dependence on glucose breakdown presents a series of targets for potential therapeutic development, many of which have been explored and validated as therapeutic targets experimentally. These include enzymes directly involved in glucose metabolism (e.g., the trypanosome hexokinases), as well as cellular components required for development and maintenance of the essential subcellular compartments that house the major part of the pathway, the glycosomes.

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