Toxoplasmosis is an opportunistic disease caused by the protozoan parasite Toxoplasma gondii. The parasite is usually staved off by a healthy immune system and remains dormant in the body. In immunocompromised patients, the parasite can become active and spread throughout the body causing symptoms such as encephalitis, cognitive disorders, seizures, and death. Combination drug therapy is the usual treatment for toxoplasmosis; however, patients suffer from problems of intolerance, allergic reactions, and cytotoxicity. In an effort to identify new drug targets for toxoplasmosis, a series of compounds have been synthesized that can be used as tools to probe the unique pathways used by T. gondii to survive in the human host. One class of these compounds is pyridinyl imidazoles, which have been shown to be active against T. gondii MAP kinases. To set up a protein pull down assay, a biotinylated linker was synthesized. We have also synthesized a compound that’s being used to study the pathways involved in the most active and proliferative form of T. gondii.
| Identifer | oai:union.ndltd.org:USF/oai:scholarcommons.usf.edu:etd-7637 |
| Date | 23 November 2015 |
| Creators | Yacoub, Jeanine |
| Publisher | Scholar Commons |
| Source Sets | University of South Flordia |
| Detected Language | English |
| Type | text |
| Format | application/pdf |
| Source | Graduate Theses and Dissertations |
| Rights | default |
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