Molecular Strategies for Active Host Cell Invasion by Apicomplexan Parasites

dc.contributor.authorTonkin, Michelle Lorine
dc.contributor.supervisorBoulanger, Martin J.
dc.date.accessioned2014-07-28T23:05:28Z
dc.date.available2015-05-31T11:22:04Z
dc.date.copyright2014en_US
dc.date.issued2014-07-28
dc.degree.departmentDepartment of Biochemistry and Microbiologyen_US
dc.degree.levelDoctor of Philosophy Ph.D.en_US
dc.description.abstractParasites of phylum Apicomplexa cause devastating diseases on a global scale. Toxoplasma gondii, the etiological agent of toxoplasmosis, and Plasmodium falciparum, the most virulent agent of human malaria, have the most substantial effects on human health and are the most widely studied. The success of these parasites is due in part to a sophisticated molecular arsenal that supports a variety of novel biological processes including a unique form of host cell invasion. Accessing the protective environment of the host cell is paramount to parasite survival and is mediated through an active invasion process: the parasite propels itself through a circumferential ring known as the moving junction (MJ) formed between its apical tip and the host cell membrane. The MJ ring is comprised of a parasite surface protein (AMA1) that engages a protein secreted by the parasite into the host cell and presented on the host cell surface (RON2). Thus, through an intriguing mechanism the parasite provides both receptor and ligand to enable host cell invasion. Prior to the studies described herein, the characterization of the AMA1-RON2 association was limited to low-resolution experiments that provided little insight into the functional and architectural details of this crucial binary complex. Towards elucidating the mechanism of AMA1-RON2 dependent invasion, I first structurally characterized T. gondii AMA1 bound to the corresponding binding region of RON2; analysis of the AMA1-RON2 interface along with biophysical data revealed an intimate association likely capable of withstanding the shearing forces generated as the parasite dives through the constricted MJ ring. To investigate the role of the AMA1-RON2 complex across genera, species and life-cycle stages, I next characterized the AMA1-RON2 complex from a distantly related genus within Apicomplexa (Plasmodium) and from a divergent pairing within T. gondii. By combining structural, biophysical and biological data, I was able to generate a detailed model describing the role of AMA1 and RON2 in MJ dependent invasion, which is currently supporting efforts to develop novel vaccines and cross-reactive small molecule therapeutics.en_US
dc.description.proquestcode0487en_US
dc.description.proquestemailtonkin.ml@gmail.comen_US
dc.description.scholarlevelGraduateen_US
dc.identifier.bibliographicCitationTonkin, M. L., M. Roques, M. H. Lamarque, M. Pugniere, D. Douguet, J. Crawford, M. Lebrun and M. J. Boulanger (2011). “Host cell invasion by apicomplexan parasites: insights from the co-structure of AMA1 with a RON2 peptide.” Science 333(6041): 463-467.en_US
dc.identifier.bibliographicCitationVulliez-Le Normand, B., M. L. Tonkin, M. H. Lamarque, S. Langer, S. Hoos, M. Roques, F. A. Saul, B. W. Faber, G. A. Bentley, M. J. Boulanger and M. Lebrun (2012). “Structural and functional insights into the malaria parasite moving junction complex.” PLoS Pathogens 8(6): e1002755.en_US
dc.identifier.bibliographicCitationPoukchanski, A., H. M. Fritz, M. L. Tonkin, M. Treeck, M. J. Boulanger and J. C. Boothroyd (2013). “Toxoplasma gondii sporozoites invade host cells using two novel paralogues of RON2 and AMA1.” PLoS One 8(8): e70637.en_US
dc.identifier.urihttp://hdl.handle.net/1828/5496
dc.language.isoenen_US
dc.rights.tempAvailable to the World Wide Weben_US
dc.subjectX-ray crystallographyen_US
dc.subjectHost-pathogen interactionsen_US
dc.subjectProtein purificationen_US
dc.subjectProtein productionen_US
dc.subjectProtein crystallizationen_US
dc.subjectApicomplexaen_US
dc.titleMolecular Strategies for Active Host Cell Invasion by Apicomplexan Parasitesen_US
dc.typeThesisen_US

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