Cyclin-dependent protein kinases as therapeutic drug targets
for antimalarial drug development.
Waters NC, Geyer JA.
United States Army Medical Research Unit-Kenya, MRU 64109 APO, AE 09831-4109,
Kenya. [email protected]
Cyclin-dependent protein kinases (CDKs) have been attractive drug targets for
the development of anticancer therapies due to their direct and crucial role in
the regulation of cellular proliferation. Following this trend, CDKs have been
pursued as potential drug targets for several other diseases. Structure-based
drug design programmes have focused on the plasmodial CDKs to develop new
candidate antimalarial compounds. This review discusses the most recent advances
relating to three Plasmodium falciparum CDKs (PfPK5, PfPK6 and Pfmrk) as they
are developed as antimalarial drug targets. CDKs are highly conserved, and focus
must be placed upon the amino acid differences between human and plasmodial CDKs
in order to develop specific inhibitors. Comparisons of the active sites of
human and parasite CDKs reveal sequence and potential structural variations.
Using sequence analysis, molecular modelling and in vitro drug screening, it is
possible to identify and develop inhibitors that specifically target the
plasmodial CDKs. These efforts are aimed at identifying new classes of CDK
inhibitors that may be exploited for antimalarial drug development.
The initiating
steps of a type II fatty acid synthase in
Plasmodium falciparum are catalyzed by pfacp, pfmcat, and pfKASIII.
Prigge ST, He X, Gerena L, Waters NC, Reynolds KA.
Molecular Microbiology and Immunology, Malaria Research Institute, Johns Hopkins
Bloomberg School of Public Health, Baltimore, Maryland 21205, USA. [email protected]
Malaria, a disease caused by protozoan parasites of the genus Plasmodium, is one
of the most dangerous infectious diseases, claiming millions of lives and
infecting hundreds of millions of people annually. The pressing need for new
antimalarials has been answered by the discovery of new drug targets from the
malaria genome project. One of the early findings was the discovery of two genes
encoding Type II fatty acid biosynthesis proteins: ACP (acyl carrier protein)
and KASIII (beta-ketoacyl-ACP synthase III). The initiating steps of a Type II
system require a third protein: malonyl-coenzyme A:ACP transacylase (MCAT). Here
we report the identification of a single gene from P. falciparum encoding pfMCAT
and the functional characterization of this enzyme. Pure recombinant pfMCAT
catalyzes malonyl transfer from malonyl-coenzyme A (malonyl-CoA) to pfACP. In
contrast, pfACP(trans), a construct of pfACP containing an amino-terminal
apicoplast transit peptide, was not a substrate for pfMCAT. The product of the
pfMCAT reaction, malonyl-pfACP, is a substrate for pfKASIII, which catalyzes the
decarboxylative condensation of malonyl-pfACP and various acyl-CoAs. Consistent
with a role in de novo fatty acid biosynthesis, pfKASIII exhibited typical KAS
(beta-ketoacyl ACP synthase) activity using acetyl-CoA as substrate (k(cat) 230
min(-1), K(M) 17.9 +/- 3.4 microM). The pfKASIII can also catalyze the
condensation of malonyl-pfACP and butyryl-CoA (k(cat) 200 min(-1), K(M) 35.7 +/-
4.4 microM) with similar efficiency, whereas isobutyryl-CoA is a poor substrate
and displayed 13-fold less activity than that observed for acetyl-CoA. The
pfKASIII has little preference for malonyl-pfACP (k(cat)/K(M) 64.9
min(-1)microM(-1)) over E. coli malonyl-ACP (k(cat)/K(M) 44.8
min(-1)microM(-1)). The pfKASIII also catalyzes the acyl-CoA:ACP transacylase (ACAT)
reaction typically exhibited by KASIII enzymes, but does so almost 700-fold
slower than the KAS reaction. Thiolactomycin did not inhbit pfKASIII (IC(50) >
330 microM), but three structurally similar substituted 1,2-dithiole-3-one
compounds did inhibit pfKASIII with IC(50) values between 0.53 microM and 10.4
microM. These compounds also inhibited the growth of P. falciparum in culture.