Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.664284
Title: Enzymes involved in malaria parasite egress
Author: Penzo , Maria
ISNI:       0000 0004 5362 5047
Awarding Body: Open University
Current Institution: Open University
Date of Award: 2014
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Abstract:
The malaria parasite is a plague of humanity. Understanding its biology and blocking essential parasite biochemical pathways are ways of controlling and possibly defeating malaria. During its complex life cycle, the parasite undergoes cycles of asexual replication in erythrocytes, then egresses from them to invade fresh erythrocytes. An essential cascade involved in egress, which includes at least two enzymes, has recently been discovered in P. Jalciparum . The parasite cGMP-dependent kinase PKG triggers the discharge of a serine protease called SUBl from secretory organelles called exonemes and its subsequent activation. SUBl cleaves several parasite substrates, enabling egress and preparing the merozoites for invasion. Blocking either enzyme inhibits egress, making them potential antimalarial targets. Whilst the most dangerous cause of human malaria is Plasmodium Jalciparum, the zoonotic species P. knowlesi can also cause severe disease and death. P. knowlesi has recently been adapted to in vitro culture in human erythrocytes, providing an excellent tool to study this human pathogen in depth. Shedding light on the specificity and regulation of P. knowlesi PKG and SUBl will provide information about an important biochemical pathwaywhich may be conserved across human Pla'smod~um species. In this study, P. knowlesi PKG was characterized using selective inhibitors of the enzyme that block egress of P. knowlesi parasites in vitro.PkSUB 1 was expressed in a recombinant enzymatically active form and new selective inhibitors of PfSUBl and PkSUBl were designed using a combination of in silico,in vitro and substrate based approaches. Some of these compounds were shown to inhibit both egress and SUB1-mediated processing of endogenous parasite substrates. The results show that the essential role of PKG and SUBl in egress is conserved in P .
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.664284  DOI: Not available
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