Realistic illustration of spinning hemozoin crystals inside a malaria parasite propelled by hydrogen peroxide reactions, like tiny rockets.
Realistic illustration of spinning hemozoin crystals inside a malaria parasite propelled by hydrogen peroxide reactions, like tiny rockets.
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Scientists identify a rocket-fuel-like reaction that propels spinning iron crystals inside malaria parasites

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University of Utah researchers report that iron-rich hemozoin crystals inside the malaria parasite Plasmodium falciparum move through the parasite’s digestive compartment because reactions involving hydrogen peroxide at the crystal surface generate chemical propulsion. The work, published in Proceedings of the National Academy of Sciences, links a long-observed phenomenon to peroxide chemistry and could point to new antimalarial drug strategies and ideas for engineered micro- and nanoscale devices.

The malaria parasite Plasmodium falciparum produces iron-containing hemozoin crystals as it detoxifies heme released during hemoglobin digestion. Researchers have long observed that these crystals move within the parasite’s digestive compartment (often called the food vacuole) while the parasite is alive and that the motion stops when the parasite dies.

In a study led by University of Utah biochemist Paul A. Sigala, the team reports evidence that the motion is driven by chemistry involving hydrogen peroxide (H_2O_2). The researchers found that hemozoin can catalyze reactions with hydrogen peroxide and that exposing isolated hemozoin crystals to hydrogen peroxide causes them to move, consistent with a chemical-propulsion mechanism.

The researchers also report that manipulating the parasite’s environment to reduce peroxide-related chemistry can slow the crystals’ movement even when the parasites remain viable. In the University of Utah’s account of the work, postdoctoral researcher Erica Hastings said the underlying peroxide-decomposition reaction is widely used in propulsion technologies, and she argued that identifying parasite-specific chemistry could open directions for drug development.

The team proposes that keeping crystals in motion could help the parasite manage oxidative stress by consuming hydrogen peroxide and could help prevent crystal aggregation, maintaining a reactive surface for processing toxic heme. The researchers describe the phenomenon as a biological example of a self-propelled metallic nanoparticle.

The study, “Chemical propulsion of hemozoin crystal motion in malaria parasites,” was published in Proceedings of the National Academy of Sciences (PNAS) in 2025 (volume 122, issue 44) and is authored by Hastings and colleagues. The findings, the researchers say, could inform efforts to design antimalarial approaches that interfere with crystal-surface chemistry and may also provide concepts relevant to engineered self-propelled particles for applications such as targeted drug delivery.

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Early reactions on X primarily consist of science enthusiasts and regular users sharing the ScienceDaily article on the rocket-fuel-like propulsion of iron crystals in malaria parasites via hydrogen peroxide reactions. Posters note potential for new antimalarial strategies and microscale engineering inspirations. Sentiments are neutral to positive, lacking controversy or diverse opinions.

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Medical illustration showing Enterococcus faecalis bacteria producing hydrogen peroxide to stall chronic wound healing, with catalase enzyme restoring skin cell migration.
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Study links Enterococcus faecalis metabolism to stalled healing in chronic wounds

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Researchers report that Enterococcus faecalis—a bacterium often found in chronic wounds—can hinder skin repair by generating hydrogen peroxide through a metabolic pathway, triggering stress responses that stop key skin cells from migrating. In laboratory experiments, breaking down the peroxide with the antioxidant enzyme catalase helped restore cell movement, suggesting a potential treatment approach that does not rely on antibiotics.

Researchers have discovered a protein called Aurora-related kinase 1 (ARK1) that is vital for the malaria parasite's cell division. Disabling ARK1 in experiments halted the parasite's ability to replicate in both human and mosquito hosts. The finding, published in Nature Communications, highlights a potential target for new antimalarial drugs.

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A genetic technology called a gene drive has shown promise in preventing malaria transmission by mosquitoes during lab tests in Tanzania. Researchers modified local mosquitoes to produce antimalarial proteins, demonstrating effective inhibition of parasites from infected children. The findings suggest the approach could work in the field if released.

Researchers in Germany have identified a rare mutation in the GPX4 enzyme that disables its protective role in neurons, allowing toxic lipid peroxides to damage cell membranes and trigger ferroptotic cell death. Studies in patient-derived cells and mice show a pattern of neurodegeneration that resembles changes seen in Alzheimer’s disease and other dementias.

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Researchers have engineered a mosquito-killing Metarhizium fungus that emits a flower-like scent, longifolene, to draw in the insects and infect them. The work, published October 24, 2025, in Nature Microbiology, could provide a safe, affordable complement to chemical pesticides amid rising mosquito-borne disease, the team says. ([doi.org](https://doi.org/10.1038/s41564-025-02155-9))

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Researchers at the University of Santiago de Compostela report a light-driven method that directly “allylates” methane—adding an allyl group that can be used to build more complex molecules—and they demonstrate the approach by producing the nonsteroidal estrogen dimestrol from methane.

 

 

 

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