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Disruption of parasite protein function and membrane integrity through the generation of free radicals, particularly reactive oxygen species (ROS). Free radicals damage cellular components such as proteins, lipids, and nucleic acids, compromising essential structures and leading to parasite death. Many antimalarial drugs exploit this vulnerability by promoting ROS production within the parasite. Targeting protein/membrane integrity via oxidative stress is a validated strategy for antiparasitic drug development.
Induction of oxidative stress and free radical-mediated damage to parasite proteins and membranes.
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