Characterization of Two EF-hand Domain-containing Proteins from Toxoplasma gondii.

The universal role of calcium (Ca(2+) ) as a second messenger in cells depends on a large number of Ca(2+) -binding proteins (CBP), which are able to bind Ca(2+) through specific domains. Many CBPs share a type of Ca(2+) -binding domain known as the EF-hand. The EF-hand motif has been well studied and consists of a helix-loop-helix structural domain with specific amino acids in the loop region that interact with Ca(2+) . In Toxoplasma gondii a large number of genes (approximately 68) are predicted to have at least one EF-hand motif. The majority of these genes have not been characterized. We report the characterization of two EF-hand motif-containing proteins, TgGT1_216620 and TgGT1_280480, which localize to the plasma membrane and to the rhoptry bulb, respectively. Genetic disruption of these genes by CRISPR (clustered regularly interspaced short palindromic repeats)/Cas9 (CRISPR-associated protein 9) resulted in mutant parasite clones (Δtg216620 and Δtg280480) that grew at a slower rate than control cells. Ca(2+) measurements showed that Δtg216620 cells did not respond to extracellular Ca(2+) as the parental controls while Δtg280480 cells appeared to respond as the parental cells. Our hypothesis is that TgGT1_216620 is important for Ca(2+) influx while TgGT1_280480 may be playing a different role in the rhoptries.