Epigenetic inhibitors as a promising new antimalarial intervention strategy? A new study identifies an inhibitor of gene regulation that specifically kills the malaria pathogen.
A multinational research team led by Professor Markus Meiβner (LMU Munich) and Professor Gernot Längst (University of Regensburg) has gained important insights into the gene regulation of Plasmodium falciparum, the main cause of malaria. Published in the journal Nature, the findings open up new opportunities for the development of innovative therapeutic approaches.
Malaria remains one of the greatest global health threats. In 2022, there were an estimated 247 million infections and over 600,000 deaths, mostly in sub-Saharan Africa. Innovative research approaches are therefore urgently needed to achieve long-term progress in prevention and treatment.
Malaria is caused by parasites of the genus Plasmodium, which is transmitted to humans through the bite of infected mosquitoes. Plasmodium falciparum, the deadliest of the malaria species, has a highly complex life cycle controlled by precise gene regulation. Understanding these regulatory processes is crucial in order to specifically combat the pathogen at different stages of development.
The team identified the chromatin remodeler PfSnf2L (a protein complex that regulates the accessibility of DNA for transcription) as a key regulator of genes that play an important role in various stages of the pathogen’s development. “Our research shows that PfSnf2L is essential for P. falciparum to dynamically adjust gene expression,” explains Maria Theresia Watzlowik, lead author of the study.
The unique sequence and functional properties of PfSnf2L led to the identification of a highly specific inhibitor