1. Onametostat, a PfPRMT5 inhibitor, exhibits antimalarial activity to Plasmodium falciparum .
- Author
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Min H, Lucky AB, Madsen JJ, Chim-Ong A, Li X, Cui L, and Miao J
- Subjects
- Erythrocytes parasitology, Erythrocytes drug effects, Protozoan Proteins antagonists & inhibitors, Protozoan Proteins metabolism, Protozoan Proteins genetics, Humans, Inhibitory Concentration 50, Histones metabolism, Malaria, Falciparum drug therapy, Malaria, Falciparum parasitology, Enzyme Inhibitors pharmacology, Plasmodium falciparum drug effects, Plasmodium falciparum growth & development, Antimalarials pharmacology, Protein-Arginine N-Methyltransferases antagonists & inhibitors, Protein-Arginine N-Methyltransferases metabolism
- Abstract
Protein arginine methyltransferases (PRMTs) play critical roles in Plasmodium falciparum , a protozoan causing the deadliest form of malaria, making them potential targets for novel antimalarial drugs. Here, we screened 11 novel PRMT inhibitors against P. falciparum asexual growth and found that onametostat, an inhibitor for type II PRMTs, exhibited strong antimalarial activity with a half-maximal inhibitory concentration (IC
50 ) value of 1.69 ± 0.04 µM. In vitro methyltransferase activities of purified PfPRMT5 were inhibited by onametostat, and a shift of IC50 to onametostat was found in the PfPRTM5 disruptant parasite line, indicating that PfPRTM5 is the primary target of onametostat. Consistent with the function of PfPRMT5 in mediating symmetric dimethylation of histone H3R2 (H3R2me2s) and in regulating invasion-related genes, onametostat treatment led to the reduction of H3R2me2s level in P. falciparum and caused the defects on the parasite's invasion of red blood cells. This study provides a starting point for identifying specific PRMT inhibitors with the potential to serve as novel antimalarial drugs., Competing Interests: The authors declare no conflict of interest. more...- Published
- 2024
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