The
O-fucosylation of the thrombospondin type I repeat (TSR) domain
is important for TSR-containing proteins’ optimal folding and
stability. However, the importance of Plasmodium O-fucosyltransferase
2 (POFut2) remains unclear due to two different reports. Here, we
disrupted the POFut2 gene in Plasmodium berghei and demonstrated that POFut2 KO parasites develop
normally in blood and mosquito stages but show reduced infectivity
in mice. We found that the reduced infectivity of POFut2 KO sporozoites was due to a diminished level of TRAP that affected
the parasite gliding motility and hepatocyte infectivity. Using all-atom
MD simulation, we also hypothesize that O-fucosylation impacts the
TSR domain’s stability more than its heparin binding capacity