Ca2+ signals critical for egress and gametogenesis in malaria parasites depend on a multipass membrane protein that interacts with PKG
More about Open Access at the CrickAuthors list
Aurélia C Balestra Kostas Kousis Natacha Klages Steven A Howell Helen R Flynn Marcus Bantscheff Carla Pasquarello Abi Perrin Lorenzo Brusini Patrizia Arboit Olalla Sanz Laura Peces-Barba Castaño Chrislaine Withers-Martinez Alexandre Hainard Sonja Ghidelli-Disse Bram Snijders David A Baker Michael Blackman Mathieu BrochetAbstract
Calcium signaling regulated by the cGMP-dependent protein kinase (PKG) controls key life cycle transitions in the malaria parasite. However, how calcium is mobilized from intracellular stores in the absence of canonical calcium channels in Plasmodium is unknown. Here, we identify a multipass membrane protein, ICM1, with homology to transporters and calcium channels that is tightly associated with PKG in both asexual blood stages and transmission stages. Phosphoproteomic analyses reveal multiple ICM1 phosphorylation events dependent on PKG activity. Stage-specific depletion of Plasmodium berghei ICM1 prevents gametogenesis due to a block in intracellular calcium mobilization, while conditional loss of Plasmodium falciparum ICM1 is detrimental for the parasite resulting in severely reduced calcium mobilization, defective egress, and lack of invasion. Our findings suggest that ICM1 is a key missing link in transducing PKG-dependent signals and provide previously unknown insights into atypical calcium homeostasis in malaria parasites essential for pathology and disease transmission.
Journal details
Journal Science advances
Volume 7
Issue number 13
Pages eabe5396
Available online
Publication date
Full text links
Publisher website (DOI) 10.1126/sciadv.abe5396
Figshare View on figshare
Europe PubMed Central 33762339
Pubmed 33762339