Biochemical and genetic analyses are required to identify potential dr
ug targets in apicomplexan parasites, but these studies have proved di
fficult in most parasite systems. We have developed methods based on e
xpression of parasite proteins in the budding yeast, Saccharomyces cer
evisiae, to vapidly screen drugs directed against particular parasite
targets, to study the structure and function of these target molecules
, and to identify mutations in the parasite genes that alter enzyme sp
ecificity or drug sensitivity. in this paper we outline the parameters
that need to be considered to design yeast strains that function effi
ciently to assay function of parasite proteins. Basic protocols and me
thods are included. We detail some problems that might be encountered
in the engineering of these yeast strains and suggest possible solutio
ns. (C) 1997 Academic Press.