Glycosylphosphatidylinositols represent the predominant class of glyco
lipids synthesized by the asexual, intraerythrocytic stages of Plasmod
ium falciparum. These glycolipids have been implicated as malarial tox
ins involved in parasite-induced release of cytokines, such as tumor n
ecrosis factor-alpha and interleukin-l. Two potential glycosylphosphat
idylinositol membrane-anchor precursors with the structures ethanolami
ne phosphate (mannose-alpha 1,2)mannose-alpha 1,2-mannose-alpha 1,6-ma
nnose-alpha 1,4-glucosamine-inositol(acyl)phosphate diacylglycerol (P.
f.alpha) and ethanolamine-phosphate-mannose-alpha 1,2-mannose-alpha 1,
6-mannose-alpha 1,4-glucosamine-inositol(acyl)phosphate diacylglycerol
(P.f.beta) have been described in P. falciparum. Only one (P.f.alpha)
has been demonstrated to serve as an anchor for merozoite surface pro
tein-1 and merozoite surface protein-2. In this report we present data
showing that asexual, intraerythrocytic stages of P. falciparum use b
oth glycosylphosphatidylinositols to anchor proteins. The synthesis of
the two glycosylphosphatidylinositol membrane anchor precursors and t
he protein-bound glycosylphosphatidylinositol anchors is tightly regul
ated and varies throughout the intraerythrocytic development of the as
exual stages of P. falciparum. The glycosylphosphatidylinositol membra
ne-anchor precursor P.f.beta is synthesized and transferred to protein
predominantly in trophozoite stages (about 30 h). (C) 1998 Academic P
ress.