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Massachusetts Institute of Technology

Exploring Protoheme IX Farnesyltransferase as an Antimalarial Drug Target

Abstract

dc:description.abstract

The search for novel antimalarials continues due to the need to combat the rapidly increasing prevalence of multidrug resistant Plasmodium species parasites that cause malaria. Recent advances in technology to genetically modify malarial parasites and methods for high throughput screening of compounds allow for increased understanding of Plasmodium biology and evaluation of potential inhibitors. The Plasmodium falciparum genome continues to be annotated and functionally characterized, including the gene encoding a protoheme IX farnesyltransferase (aka PfCOX10). This enzyme is a critical component of heme O synthesis. Since heme O is a necessary precursor to heme A, a critical cofactor of cytochromes within the mitochondrial electron transport chain (ETC), we infer that function of PfCOX10 is related to ETC-dependent essential processes such as pyrimidine biosynthesis. In this work, we take advantage of modern techniques to explore PfCOX10 as a potential new target of antimalarial compounds. Parasites with conditional knockdown of PfCOX10 are screened for growth against compounds known to interact with heme, as well as the 400-compound Pathogen Box collection from the Medicines for Malaria Venture (MMV). We identify a modest interaction of PfCOX10 with antimalarial DSM1, as well as several compounds from the MMV Pathogen Box. The data ultimately point to utility in further exploration of PfCOX10 as a potential antimalarial drug target and for deepening biological understanding of these disease-causing parasites.

Degree

thesis:*
Name thesis:degree_name
Master
Department dc:contributor.department
Massachusetts Institute of Technology. Microbiology Graduate Program
Grantor dc:publisher
Massachusetts Institute of Technology
Year dc:date.issued
2021

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Edelen, Samantha Leigh
Advisor dc:contributor.advisor
  • Niles, Jacquin C.

Rights

dc:rights
Statement dc:rights
  • In Copyright - Educational Use Permitted
  • Copyright MIT

Identifiers

dc:identifier.*
Handle dc:identifier.uri
https://hdl.handle.net/1721.1/140177
OAI identifier oai:identifier
oai:dspace.mit.edu:1721.1/140177

Chain of custody

source
Harvested from
MIT
Base URL
dspace.mit.edu/oai/request
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
related terms
citation

Edelen, Samantha Leigh. Exploring Protoheme IX Farnesyltransferase as an Antimalarial Drug Target. Massachusetts Institute of Technology, 2021. https://hdl.handle.net/1721.1/140177