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Target indicators and mechanistic function of epidrugs with activity against multiple stages of Plasmodium falciparum parasites

Dissertation (MSc (Biochemistry))--University of Pretoria, 2021.

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Other Authors: Birkholtz, Lyn-Marie
Format: Thesis
Language:English
Published: University of Pretoria 2022
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access_status_str Open Access
author2 Birkholtz, Lyn-Marie
author_browse Birkholtz, Lyn-Marie
author_facet Birkholtz, Lyn-Marie
collection Thesis
dc_rights_str_mv © 2022 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria.
description Dissertation (MSc (Biochemistry))--University of Pretoria, 2021.
format Thesis
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institution University of Pretoria (South Africa)
language English
last_indexed 2026-06-10T12:37:22.799Z
license_str Other — see source repository
provenance_str_mv Harvested via OAI-PMH from UPSpace — University of Pretoria Institutional Repository
publishDate 2022
publishDateRange 2022
publishDateSort 2022
publisher University of Pretoria
publisherStr University of Pretoria
record_format dspace
source_str UPSpace — University of Pretoria Institutional Repository
spelling oai:repository.up.ac.za:2263/83937 Target indicators and mechanistic function of epidrugs with activity against multiple stages of Plasmodium falciparum parasites Birkholtz, Lyn-Marie daniel.opperman@gmail.com Reader, Janette Opperman, Daniel Francis Luke Biochemistry Plasmodium falciparum parasites Epidrugs UCTD Dissertation (MSc (Biochemistry))--University of Pretoria, 2021. Resistance to the most widely used drugs in the treatment of malaria, those in artemisinin-based combination therapies, has emerged, most recently in Africa. Development of new drugs that exploit unique structures with new modes of action (MoA) is therefore critical. There is also a need for the development of compounds with transmission-blocking activity, in addition to the clearance of symptom-causing stages associated with drugs currently part of the chemotherapeutic toolbox. A promising avenue of research in this regard is into epigenetic drugs (“epidrugs”), which target epigenetic mechanisms of transcriptional control, resulting in parasite death through perturbation of gene expression. A selection of compounds with demonstrated epigenetic perturbation in human cancer cell lines have shown favourable inhibitory profiles against Plasmodium falciparum parasites. For a number of these compounds, the specific mode of action remained to be elucidated and characterised. This dissertation has contributed to our understanding of these compounds’ modes of action, demonstrating perturbation of histone post-translational modifications, and revealing possible binding modes to putative targets through in silico predictions. Findings confirmed histone deacetylase inhibition for both Scriptaid and Sirtinol, with histone deacetylase 1 (PfHDAC1) and sirtuin 2A (PfSir2A), respectively, indicated as the targets of these compounds through in silico docking studies. ML324 was found to exhibit histone demethylase activity in P. falciparum late-stage gametocytes, with PfJmj3 indicated as the target of this compound. Finally, the potential of these compounds as transmission-blocking drugs has been revealed through exflagellation inhibition assays and confirmed with standard membrane-feeding assays. These results underscore the potential of epigenetic transcriptional control as a targetable biology, and of epidrugs to contribute towards addressing the development of drug resistance by P. falciparum. The findings demonstrated in this dissertation may lay the groundwork for future drug development efforts for which the epigenetic drugs discussed here may serve as chemical scaffolds. National Research Foundation (NRF) Biochemistry MSc (Biochemistry) Unrestricted 2022-02-15T12:56:47Z 2022-02-15T12:56:47Z 2022 2021 Dissertation * A2022 http://hdl.handle.net/2263/83937 en © 2022 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria. application/pdf University of Pretoria
spellingShingle Biochemistry
Plasmodium falciparum parasites
Epidrugs
UCTD
Target indicators and mechanistic function of epidrugs with activity against multiple stages of Plasmodium falciparum parasites
title Target indicators and mechanistic function of epidrugs with activity against multiple stages of Plasmodium falciparum parasites
title_full Target indicators and mechanistic function of epidrugs with activity against multiple stages of Plasmodium falciparum parasites
title_fullStr Target indicators and mechanistic function of epidrugs with activity against multiple stages of Plasmodium falciparum parasites
title_full_unstemmed Target indicators and mechanistic function of epidrugs with activity against multiple stages of Plasmodium falciparum parasites
title_short Target indicators and mechanistic function of epidrugs with activity against multiple stages of Plasmodium falciparum parasites
title_sort target indicators and mechanistic function of epidrugs with activity against multiple stages of plasmodium falciparum parasites
topic Biochemistry
Plasmodium falciparum parasites
Epidrugs
UCTD
url http://hdl.handle.net/2263/83937