- Open Access
Biochemical and functional characterization of Plasmodium falciparum DNA polymerase δ
© Vasuvat et al. 2016
Received: 14 October 2015
Accepted: 11 February 2016
Published: 24 February 2016
Emergence of drug-resistant Plasmodium falciparum has created an urgent need for new drug targets. DNA polymerase δ is an essential enzyme required for chromosomal DNA replication and repair, and therefore may be a potential target for anti-malarial drug development. However, little is known of the characteristics and function of this P. falciparum enzyme.
The coding sequences of DNA polymerase δ catalytic subunit (PfPolδ-cat), DNA polymerase δ small subunit (PfPolδS) and proliferating cell nuclear antigen (PfPCNA) from chloroquine- and pyrimethamine-resistant P. falciparum strain K1 were amplified, cloned into an expression vector and expressed in Escherichia coli. The recombinant proteins were analysed by SDS-PAGE and identified by LC–MS/MS. PfPolδ-cat was biochemically characterized. The roles of PfPolδS and PfPCNA in PfPolδ-cat function were investigated. In addition, inhibitory effects of 11 compounds were tested on PfPolδ-cat activity and on in vitro parasite growth using SYBR Green I assay.
The purified recombinant protein PfPolδ-cat, PfPolδS and PfPCNA showed on SDS-PAGE the expected size of 143, 57 and 34 kDa, respectively. Predicted amino acid sequence of the PfPolδ-cat and PfPolδS had 59.2 and 24.7 % similarity respectively to that of the human counterpart. The PfPolδ-cat possessed both DNA polymerase and 3′–5′ exonuclease activities. It used both Mg2+ and Mn2+ as cofactors and was inhibited by high KCl salt (>200 mM). PfPolδS stimulated PfPolδ-cat activity threefolds and up to fourfolds when PfPCNA was included in the assay. Only two compounds were potent inhibitors of PfPolδ-cat, namely, butylphenyl-dGTP (BuPdGTP; IC50 of 38 µM) and 7-acetoxypentyl-(3, 4 dichlorobenzyl) guanine (7-acetoxypentyl-DCBG; IC50 of 55 µM). The latter compound showed higher inhibition on parasite growth (IC50 of 4.1 µM).
Recombinant PfPolδ-cat, PfPolδS and PfPCNA were successfully expressed and purified. PfPolS and PfPCNA increased DNA polymerase activity of PfPolδ-cat. The high sensitivity of PfPolδ to BuPdGTP can be used to differentiate parasite enzyme from mammalian and human counterparts. Interestingly, 7-acetoxypentyl-DCBG showed inhibitory effects on both enzyme activity and parasite growth. Thus, 7-acetoxypentyl-DCBG is a potential candidate for future development of a new class of anti-malarial agents targeting parasite replicative DNA polymerase.
Malaria remains one of the major global public health problems in more than 100 endemic countries. Even though the numbers of malaria cases are decreasing, in 2013 there were still 198 million estimated cases globally and 584,000 deaths, mainly among sub-Saharan African children under 5 years of age . Plasmodium falciparum is the most virulent human malaria parasite responsible for the majority of mortality cases. The emergence of anti-malarial resistance, in particular to artemisinins, has become a problem in malarial treatment and control [2–4]. Therefore, a better understanding of parasite metabolism, leading to identification of enzymes essential for its survival, should help in finding new targets for drug development.
One of the chemotherapeutic targets of interest is malarial DNA polymerase, which is an enzyme directly involved in polymerization of deoxynucleotides during replication and/or repair of cellular genetic material . Eukaryotes possess 4 polymerases of the B-family, three of which, namely, DNA polymerase α (Pol α), DNA polymerase δ (Pol δ) and DNA polymerase ε (Pol ε), are essential enzymes for nuclear DNA replication . Each enzyme plays a role in the replisome complex located at the replication fork, in which Pol δ replicates the lagging strand after it has been primed by Pol α . Both Pol δ and Pol ε are distinguished from Pol α by their 3′–5′ proof-reading exonuclease activity, which allows removal of mis-incorporated deoxynucleotides, ensuring a high fidelity of DNA synthesis required for accurate genome replication .
Pol δ holoenzyme participates in replicative synthesis in concert with the processivity factor proliferating cell nuclear antigen (PCNA). Kinetic and binding studies have shown that PCNA increases Pol δ processivity as well as activity , possibly by forming a trimeric closed ring structure, which encircles the DNA and provides a sliding clamp for attachment of Pol δ . In addition to its function in DNA replication, Pol δ plays a role in DNA repair and recombination . In base excision repair (BER), one of DNA repair mechanisms of single-stranded DNA damage, Pol δ is involved in the long-path pathway, whereas Pol β plays a role in the short-path pathway . Interestingly, the long-patch BER is predominate in P. falciparum while short-path BER is mainly found in humans .
Pol δ has been purified from a number of eukaryotes. In Saccharomyces cerevisiae, Pol δ is composed of three subunits: catalytic subunit Pol3p and structural subunits Pol31p and Pol32p [12–14]. In Schizosaccharomyces pombe, Pol δ consists of four subunits: Pol3, Cdc 1, Cdc27 and Cdm1 . Human and mammalian enzymes initially were characterized as a heterodimer of p125 catalytic and p50 subunits [16, 17]. The p125 catalytic subunit is homologous to yeast Pol3 and Pol3p, whereas subunit p50 is a homologue of Cdc 1 and Pol31p [18, 19]. Later, two additional subunits of human and mammalian Pol δ were identified, namely, p68 and p12, displaying significant homology with Schizosaccharomyces pombe Cdc27 and Cdm1 respectively [20, 21]. Unlike mammalian Pol δ holoenzyme, formed by four subunits , only two subunits (p125 catalytic subunit and p50 small subunit) were identified in the Plasmodb sequence database.
Three types of P. falciparum DNA polymerases have been identified and characterized: nuclear Pol α and Pol β from parasite crude extract [22, 23] and Pol γ from parasite mitochondria . Plasmodium falciparum (Pf)Pol δ gene of 3282 bp is located on chromosome 10 and encodes a protein of 1094 amino acids with 45 % similarity to Saccharomyces cerevisiae Pol δ [25, 26]. PfPol δ is expressed mainly in late trophozoite and schizont stages , but little is known about its enzymology and biochemical characteristics.
This study describes the cloning and expression of PfPol δ catalytic subunit (PfPolδ-cat) and the characterization of its activity in presence of its small subunit (PfPolδS) and proliferating cell nuclear antigen (PfPCNA). In addition, the in vitro inhibitory effects of 11 synthetic compounds on both recombinant PfPolδ-cat and parasite growth were evaluated for their potential as antiplasmodial drugs.
Plasmodium falciparum strain K1, a chloroquine- and pyrimethamine-resistant strain from Thailand  was cultivated in RPMI 1640 medium (Invitrogen™, CA, USA) supplemented with 10 % human serum and human red blood cell (RBC) at 37 °C under an atmosphere of 5 % CO2. Plasmodium falciparum cultures containing mostly trophozoite and schizont stages were harvested when parasitaemia was >10 % by centrifugation at 500×g for 10 min at 25 °C.
Construction of PfPolδ-cat, PfPolδS and PfPCNA1 expression vectors
Genomic DNA of P. falciparum strain K1 was used as template to generate full-length PfPolδ-cat, PfPolδS and PfPCNA1. Amplification of PfPolδ-cat was carried out using PfPolδ-cat-forward (5′-CACCCATGGAAGAACTGAAAAC-3′) and PfPolδ-cat-reverse (5′-CCAATCCATTCTTAATGAGGT-3′) primers and Phusion®High-Fidelity DNA polymerase (Thermo Scientific, MA, USA) together with 30 cycles of PCR consisting of 98 °C for 1 min, 63 °C for 10 s and 72 °C for 105 s. PfPolδS was amplified using PfPolδS-forward (5′-CACCATGGACGAAAAAGTAACAAAC-3′) and PfPolδ-p50-reverse (5′-TTTGTCTTCGTCAATTTGAAAAGTC-3′) primers and Platinum® Pfx DNA polymerase (Invitrogen™) together with 35 cycles of PCR consisting of 95 °C for 1 min, 56 °C for 40 s and 72 °C for 2 min. Pf-PCNA1 was amplified using primers previously described  and Phusion®High-Fidelity DNA polymerase together with 35 cycles of PCR consisting of 98 °C for 10 min, 58 °C for 5 s and 72 °C for 30 s. Amplicons were analysed either by 0.8 or 1.5 % agarose gel-electrophoresis. Amplified full-length PfPolδ-cat and PfPolδS was cloned into pBAD202/D TOPO® and pET101/D TOPO® expression vector (Invitrogen™), respectively. The constructed vectors, pBAD-PfPolδ-cat and pET-PfPolδS, were validated by nucleotide sequencing. Amplified full-length Pf-PCNA1 was cloned into pQE-30 expression vector and named pQE-30-PfPCNA1.
Expression and purification of PfPolδ-cat, PfPolδS and PfPCNA1
pBAD-PfPolδ-cat vector was transfected into E. coli LMG194 cells, which were grown in LB medium containing 50 μg/ml kanamycin at 37 °C with shaking until optical density of 600 nm reached 0.8. Then cells were induced by an addition of 0.002 % (w/v) L-arabinose and further incubated at 22 °C for 16–18 h. Cells were sedimented at 4 °C and then re-suspended in 3.5 volumes of cold lysis buffer (20 mM Tris–HCl pH 8.0 and 100 mM NaCl) per g of bacterial pellet. Cells were lysed using XL 2020 Sonicator® Ultrasonic Processor XL (Heat System Inc., NY, USA), centrifuged at 10,000×g for 30 min at 4 °C. Supernatant was incubated with Q Sepharose Fast Flow (GE Healthcare, UK) on ice for 10 min to remove bacterial DNA and then applied onto 1-ml HisTrap HP column (GE Healthcare) prior equilibration with buffer A (20 mM Tris–HCl pH 8.0, 300 mM NaCl) containing 10 mM imidazole. The column was washed with buffer A containing 50 mM imidazole and enzyme was eluted with 250 mM imidazole-containing buffer A. Protein purity was analysed by SDS-PAGE.
pET-PfPolδS vector was used to transform E. coli BL21 (DE3) cells, which were grown in LB media containing 100 μg/ml ampicillin, and induced with 0.25 mM isopropyl β-D-1-thiogalactopyranoside (IPTG) at 22 °C for 16 h with shaking. Cells were collected and lysed as described previously. Supernatant was applied onto 1-ml HisTrap HP column and recombinant PfPolδS was eluted using a linear gradient of 20–250 mM imidazole in buffer A. Fractions of 0.25 ml were collected and analysed by SDS–PAGE.
pQE-30-PfPCNA1 was transfected into JM109 E. coli cells, which were grown in LB medium, induced with 1 mM IPTG at 25 °C for 16 h, collected and lysed as described above. Supernatant was incubated with Ni–NTA agarose affinity beads (QIAGEN, Hilden, Germany) at 4 °C for 2 h. The sample then was applied onto a gravity column, washed and protein eluted. The flow-through, wash and eluted fractions were collected, and analysed by SDS-PAGE. Protein concentrations were measured using Bradford assay  with bovine serum albumin (BSA) as standard.
Western blotting and LC–MS/MS
After SDS-PAGE, proteins were electro-transferred onto Hybond-P PVDF membrane (GE Healthcare) and incubated at 4 °C overnight in phosphate-buffered saline (PBS) containing 5 % skim milk (blocking buffer). After washing three times with 0.05 % Tween-20 PBS buffer, membrane was incubated with mouse anti-His antibodies (Invitrogen) at 1:5000 dilution in blocking buffer at room temperature for 2 h. After washing, membrane was incubated with horseradish peroxidase-conjugated goat anti-mouse IgG for 1.5 h at room temperature and immunoreactive bands visualized using SuperSignal™ West Pico Chemiluminescent Substrate (Thermo Scientific). The expected protein bands were excised from gels and digested with trypsin. Patterns of peptide fragments and amino acid sequences were analysed using LC–MS/MS equipped with MASCOT software.
DNA polymerase assay
DNA polymerase activity was assayed using activated calf thymus DNA (CT-DNA) (Sigma-Aldrich, MA, USA) as substrate. DNA polymerase assay was conducted in a 50-μl reaction mixture containing 10 μg of activated CT-DNA, 20 mM potassium phosphate buffer pH 8, 10 mM MgCl2, 2 mM DTT, 10 μg BSA, 50 μM each of dGTP, dATP and dCTP, 1 μM dTTP, 2.5 μM [α-32P]dTTP (800 Ci/mmol; PerkinElmer, MA, USA), and 42 nM PfPolδ-cat. After incubation for 1 h at 37 °C, the reactions were terminated by adding a 250-μl mixture of 20 mM EDTA, 0.1 mg/ml BSA and 100 μl of 50 % trichloroacetic acid (TCA), followed by sedimentation. The precipitate was then washed twice with 1 % TCA and [32P]dTMP incorporation was measured in a 1450 MicroBeta® Trilux Liquid Scintillation Counter (Perkin Elmer). One unit of DNA polymerase activity is defined as the amount of enzyme that catalyzes the incorporation of 1 nmol of dTMP into DNA in 1 h at 37 °C.
Effects of divalent ions and KCl on PfPolδ-cat activity
The effects of divalent cations, Mg2+ and Mn2+, on PfPolδ-cat activity were determined in the presence of 0.3 μM PfPolδ-cat and 0–50 mM MgCl2 or MnCl2 in the polymerase assay. The effect of KCl was determined over the range 0–400 mM.
3′–5′ exonuclease assay
The 3′–5′ exonuclease activity of PfPolδ-cat was measured from the release of [α-32P]dTMP from 3′ labelled poly(dA.dT) . Substrate was prepared by incubating 125 μg/ml poly(dA.dT) with 5000 U/ml Klenow enzyme (New England Biolabs, MA, USA), 10 μM [α-32P]dTTP in 50 mM potassium phosphate pH 7.5, 5 mM MgCl2, 1 mM dAMP, and 0.5 mM β-mercaptoethanol. After incubation for 20 min at 37 °C, the reaction was termination by an addition of 10 mM EDTA and 1 M NaCl. The mixture was heated at 65 °C for 30 min and unincorporated [α-32P]dTTP removed employing AutoSeq™ G-50 dye terminator removal kit (GE Healthcare). For detection of exonuclease activity, a 30-μl reaction mixture containing 50 mM HEPES pH 7.0, 40 μg/ml BSA, 10 % glycerol, 2 mM MgCl2, 1.25 µg of 3′-labelled poly(dA.dT), and 0.2 μM PfPolδ-cat was incubated for 20 min at 37 °C and radioactivity measured as described above.
Processivity of PfPolδ-cat was determined using 500 ng of (dA)1500.(dT)12 (50:1 nucleotide ratio) as template-primer. The dT12 primer was at 5′ labelled with [γ-32P]dATP using T4 polynucleotide kinase and annealed to poly (dA)1500. Reaction mixture consisting of 20 mM Tris–HCl pH 9.0, 10 mM MgCl2, 0.2 mg/ml BSA, 2 mM DTT, 50 μM dTTP, and 42 nM PfPolδ-cat was incubated at 37 °C for 30 min. The product was precipitated with ethanol, dried, dissolved in sample buffer (95 % deionized formamide, 25 mM EDTA and 0.01 % bromophenol) and electrophoresed in 8 % polyacrylamide gel containing 7 M urea. Gel was exposed overnight to X-ray film at −80 °C.
Effects of PfPolδS and PfPCNA1 on PfPolδ-cat activity
PfPolδS (0–1 μM) was added to a standard DNA polymerase assay containing 0.15 μg of polydA.oligodT and 1 μM PfPCNA1 and incubated at 37 °C for 30 min. The reaction mixtures were processed as described.
Inhibitory effects of synthetic compounds on PfPolδ-cat activity
Inhibitory activity of 11 compounds consisting of substrate and nucleotide analogs and potential active site occupiers of PfPolδ-cat were compared with known Pol δ inhibitors, aphidicolin and N-ethylmaleimide (NEM). Stock solution (6 mM) of aphidicolin was prepared in dimethylsulfoxide (DMSO) and that of NEM (400 mM) in absolute ethanol. Stock solutions (10 mM) of N 2 -(4-butylphenyl)-2′-deoxyguanosine 5′-triphosphate (BuPdGTP), N 2 -(4-butylphenyl)- 2′-deoxyguanosine 5′-(P 2 ,P 3 -carbonyltriphosphonate) (BuPdGMPPCOP), N 2 -ethyl-2′-deoxyguanosine 5′-triphosphonate (EtdGTP), N 2 -hexyl-2′-deoxyguanosine 5′-triphosphate (HexdGTP) and Acyclovir triphosphate (ACV-TP) were prepared in sterile distilled water, while those of 2-amino-4-chloro-6-(3,4-dichloroanilino)pyrimidine, 2-amino-4-chloro-6-(3,5-dichloroanilino)pyrimidine, N2-(3,4-dichlorobenzyl)guanine (DCBG), N2-(3-fluoro,4-chlorobenzyl)guanine, 3-(4-hydroxybutyl)-6-(3-ethyl-4-methylanilino)uracil (HB-EMAU), and 7-acetoxypentyl-(3,4-dichlorobenzyl)guanine (7-acetoxypentyl-DCBG) were prepared in DMSO. All stock solutions were stored at −20 °C until used. Test concentrations of compounds were prepared by diluting stock solution with 10 mM Tris–HCl pH 8.0 and evaluated in triplicate. Compounds were added directly to the reaction mixtures except for NEM that was pre-incubated with enzyme for 30 min on ice before addition to the reaction mixture. Polymerase activity assays were conducted as described above.
Inhibition of intra-erythrocytic P. falciparum growth in culture
Plasmodium falciparum K1 strain was synchronized at ring stage using 5 % D-sorbitol treatment and then mixed with culture medium containing RPMI 1640 medium supplement with 10 % human serum. Twofold serial dilutions of each test compound were evaluated in triplicate. Parasite growth was determined by a SYBR Green I-based assay [31, 32]. Dose–response curves and IC50 values were obtained using SigmaPlot 12.0.
Expression and purification of recombinant PfPolδ-cat, PfPolδS and PfPCNA1
Amino acid sequence similarity of PfPolδ-cat compared with Polδ from other organisms
Accession number of NCBI protein reference sequence
P. falciparum 3D7
Plasmodium vivax Sal-1
S. cerevisiae S288c
Amino acid sequence similarity of PfPolδS compared with other organisms
GenBank accession no.
P. falciparum 3D7
P. knowlesi strain H
Candida dubliniensis CD36
Biochemical characterization of PfPolδ-cat
Effects of PfPolδS and PfPCNA1 on PfPolδ-cat polymerase activity
Processivity of PfPolδ-cat
Effects of inhibitors on DNA polymerase activity of PfPolδ-cat and parasite growth
Inhibitory effects (IC50) of compounds on PfPolδ-cat activity and in vitro malaria parasite growth
38.0 ± 1.7
85.6 ± 3.7
55.0 ± 3.4
4.1 ± 0.2
104.0 ± 5.6
3.8 ± 0.3
185.0 ± 7.7
34.4 ± 0.4
173.4 ± 2.7
157.8 ± 3.4
86.4 ± 0.2
347.2 ± 8.3
8.8 ± 0.5
7.4 ± 0.3
10.2 ± 0.4
Since 1976, when, for the first time, Pol δ was described in bone marrow as a novel DNA polymerase possessing a 3′–5′ proofreading exonuclease activity , eukaryotic Polδs have been purified and characterized from several organisms [16, 17, 34], with the exception of malarial parasites.
PfPolδ partially purified from parasite crude extract using Hitrap Capto Q and Hitrap Heparin columns in a fast protein liquid chromatography (FPLC) system exhibited 3′–5′ exonuclease activity and was sensitive to aphidicolin and NEM (unpublished). However, possible co-purification of PfPolε could not be rule out. Subsequent purification of PfPolδ to near homogeneity was hampered by very low recovery yield and a lack of Pol δ-specific affinity column able to separate it from PfPolε. Therefore, in this study a DNA recombinant approach was used to study PfPolδ catalytic subunit, in the presence of its small subunit PfPolδS and PfPCNA. Moreover, recombinant techniques provided sufficient amounts of enzyme to allow testing as a potential anti-malarial drug target.
Recombinant PfPolδ was successfully cloned and heterologously expressed in E. coli, but the expressed protein was produced in an insoluble form at 37 °C. The expression condition was optimized by reducing expression temperature, which usually increases soluble protein yield . The size of expressed PfPolδ-cat was 126 kDa, comparable to 130 kDa of E. coli Pol III  and 125 kDa of purified human enzyme . Tandem mass spectrometry of trypsinized recombinant PfPolδ revealed seven peptides that showed high homology with the sequence of DNA polymerase δ catalytic subunit of P. falciparum strain 3D7. Characterization of recombinant PfPolδ-cat showed that it possesses both DNA polymerase activity and 3′–5′ exonuclease activity, as found in other mammalian Polδs [16, 17, 34].
PCNA functions as a processivity factor for Pol δ by forming a molecular sliding clamp and also plays a crucial role in DNA transactions where it acts as a scaffold for the recruitment and organization of protein complexes involved in both DNA replication and repair . A previous study of protein–protein interactions of human Pol δ-PCNA complex suggested that the interaction between Pol δ and PCNA likely happens through multiple contacts via its four subunits, p12, p50, p68, and p125 [19, 37]. In this study, PfPolδ-cat polymerase activity was stimulated threefolds with the addition of PfPolδS and fourfolds in the presence of both PfPolδS and PfPCNA. The magnitude of malarial enzyme activity stimulation is comparable to those obtained from examination of the effect of human recombinant p50 on the activity of DNA polymerase δ, showing that p50 is able to slightly stimulate (about twofold) the activity of the recombinant 125 kDa catalytic subunit in the absence of PCNA, while in the presence of PCNA polymerase activity is stimulated about fivefold . In addition, a combination of PfPolδ-cat, PfPolδS and PfPCNA1 demonstrated highest processivity compared with individual protein or incomplete combination. These findings are consistent with previous report indicating that small subunit p50 is required for mediation of the interaction of human Pol δ catalytic subunit (p125) with PCNA . In this study, replication factor C (RFC) or clamp loader of P. falciparum was not used in the assay with PfPolS and PCNA, and thus higher activity of PfPolδ-cat would be expected upon addition of RFC as the latter is responsible for loading PCNA onto DNA during DNA replication . In addition to its important function in DNA replication, a role of PfPolδ-cat in base excision repair should be investigated when additional enzymes or proteins in parasite BER pathway become available.
All DNA polymerases use the same two metal cations (usually Mg2+) as co-factors for dNTP polymerization. In this study, PfPolδ-cat was able to use both Mg2+ and Mn2+ and could be activated by 5 mM Mg2+ as found for both human and calf thymus Pol δ [16, 17]. However, in the case of Mn2+, optimal concentration (2.5 mM) required by the parasite enzyme was five- to eightfold higher than that optimal for human and calf thymus Pol δ (0.3–0.5 mM) .
PfPolδ activity was differently affected by salt concentrations compared with calf thymus and human recombinant enzymes. The maximal polymerase activity of PfPolδ-cat was at 100 mM KCl and declined at higher concentrations (>200 mM). These findings are different from those observed with recombinant human and calf thymus Pol δ, where only 50 and 38 % of enzyme activity respectively was found at 50 mM KCl [16, 39]. Unlike the human and calf thymus enzymes, Pol δ of Drosophila is slightly stimulated by low KCl concentration (25 mM) . Recombinant Pol3 of Schizosaccharomyces pombe shows maximal activity at 240 mM KCl, whereas its native form is sensitive to high salt concentration . It is possible that KCl may help stabilize protein at a concentration suitable for function or to reduce its self-aggregation.
Only 4 of 11 synthetic compounds showed inhibitory effects on PfPolδ-cat activity when compared with known DNA polymerase inhibitors such as aphidicolin and NEM. The most potent inhibitor of PfPolδ-cat was BuPdGTP, which strongly inhibited mammalian Pol α compared with Pol δ and ε . In contrast to BuPdGTP, 2-amino-4-chloro-6-(3′,4′-dichloroanilino)pyrimidine showed low inhibitory effect on PfPolδ-cat but was the most potent inhibitor of parasite growth in culture. Inhibition of PfPolδ-cat activity by these two compounds did not directly correlate with parasite growth inhibition, suggesting that they may have different cell permeability and metabolic properties. However, 7-acetoxypentyl-DCBG was the most potent inhibitor of both PfPolδ-cat activity and parasite growth. Recently, 7-acetoxypentyl-DCBG was shown to be a potent antibiotic, showing an MIC of 1.25 μg/ml and a clear dose–response effect (80 % mice survived after treatment with an IP dose of 60 mg/kg) . Taken together, 7-acetoxypentyl-DCBG is a promising starting template for future rational design of a selective inhibitor against PfPolδ and may lead to development of novel anti-malarial agents.
Recombinant PfPolδ-cat, PfPolδS and PfPCNA1 were successfully expressed heterologously. PfPolδ-cat contains both DNA polymerase and 3′–5′ exonuclease activity as found in the human counterpart. However, recombinant PfPolδ-cat and PfPolδS differ from human enzymes in their deduced amino acid sequences. A combination of PfPolS and PfPCNA clearly stimulated PfPolδ-cat DNA polymerase activity and processivity. Recombinant PfPolδ-cat was inhibited by two guanine analogs, namely, BuPdGTP and 7-acetoxypentyl-DCBG. Furthermore, 7-acetoxypentyl-DCBG was demonstrated to be a potent inhibitor of in vitro malaria parasite growth. Analogs of this compound should further be developed into more potent anti-malarial drugs.
JV performed most of the laboratory work and manuscript preparation. AM performed some laboratory work on the small subunit of the enzyme. SM, UL and SP participated in designing molecular work and editing the manuscript. FF was involved in study design of enzyme function, discussion and editing the manuscript. GEW performed compound synthesis and editing of the manuscript. PCP was involved in study design, data analysis, discussion and editing of the manuscript. All authors read and approved the final manuscript.
We thank Ms. Kanthinich Thima, Department of Protozoology, Faculty of Tropical Medicine, Mahidol University for technical assistance in parasite culture. This study was supported by the National Science and Technology Development Agency (NSTDA), Ministry of Science and Technology of Thailand (Grant no. BT-B-01-MG-14-5117). JV was recipient of a scholarship from the Royal Golden Jubilee (RGJ) Ph.D. program, The Thailand Research Fund (TRF) and Mahidol University (grant no. PHD/0167/2549).
The authors declare that they have no competing interests.
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