Plasmodium falciparum UvrD activities are downregulated by DNA-interacting compounds and its dsRNA inhibits malaria parasite growth
© Tarique et al.; licensee BioMed Central Ltd. 2014
Received: 22 January 2014
Accepted: 31 March 2014
Published: 3 April 2014
Human malaria parasite infection and its control is a global challenge which is responsible for ~0.65 million deaths every year globally. The emergence of drug resistant malaria parasite is another challenge to fight with malaria. Enormous efforts are being made to identify suitable drug targets in order to develop newer classes of drug. Helicases play crucial roles in DNA metabolism and have been proposed as therapeutic targets for cancer therapy as well as viral and parasitic infections. Genome wide analysis revealed that Plasmodium falciparum possesses UvrD helicase, which is absent in the human host.
Recently the biochemical characterization of P. falciparum UvrD helicase revealed that N-terminal UvrD (PfUDN) hydrolyses ATP, translocates in 3’ to 5’ direction and interacts with MLH to modulate each other’s activity. In this follow up study, further characterization of P. falciparum UvrD helicase is presented. Here, we screened the effect of various DNA interacting compounds on the ATPase and helicase activity of PfUDN. This study resulted into the identification of daunorubicin (daunomycin), netropsin, nogalamycin, and ethidium bromide as the potential inhibitor molecules for the biochemical activities of PfUDN with IC50 values ranging from ~3.0 to ~5.0 μM. Interestingly etoposide did not inhibit the ATPase activity but considerable inhibition of unwinding activity was observed at 20 μM. Further study for analyzing the importance of PfUvrD enzyme in parasite growth revealed that PfUvrD is crucial/important for its growth ex-vivo.
As PfUvrD is absent in human hence on the basis of this study we propose PfUvrD as suitable drug target to control malaria. Some of the PfUvrD inhibitors identified in the present study can be utilized to further design novel and specific inhibitor molecules.
KeywordsATPase Helicase Malaria parasite UvrD DNA unwinding DNA interacting agents
Human malaria is the parasitic disease caused by five different species of Plasmodium (Plasmodium falciparum, P. vivax, P. ovale, P. malarie and P. knowlesi), among them P. falciparum is responsible for the most severe and lethal infection (reviewed by ). There is controversy over the number of human deaths due to malaria but as per WHO report malaria is responsible for ~0.65 million deaths every year [2, 3]. The efforts to identify suitable drug targets to fight with malaria parasite infections are a global concern [1, 4] as many previous attempts have been unsuccessful to develop new class of antimalarial drugs. Similarly the attempts to develop vaccine for malaria are not very promising and a vaccine for malaria is not possible in near future [2, 5, 6]. There are certainly limited drugs available for treatment of malaria that includes chloroquine, sulphadoxine, pyrimethamine and derivatives. During the last few years the situation has worsened mainly due to the emergence of malaria parasite resistant to several anti-malarial drugs and their spread in other region of the world [7–9]. Thus it is equally important to explore the underlying cause of the emergence of drug resistant parasite and development of novel therapeutics to treat the resistant malaria parasite infections. Although many putative therapeutic targets for malaria have been reported in the recent past [10–19] but further studies are required in order to get the insight for the successful development of suitable drugs. Helicases have also been proposed as suitable drug targets for human cancers as well as many pathogens including viruses and P. falciparum [20–33].
Helicases are molecular motor proteins that play important roles in the metabolism of nucleic acids. It is well established that in-vivo each helicase is specialized for its own helicase activity led biochemical role. The genome wide analysis of P. falciparum helicases revealed that the parasite contains a UvrD helicase while this enzyme is absent in human host [34, 35]. Later, the biochemical characterization of this P. falciparum specific UvrD helicase revealed its characteristic biochemical activities .
UvrD helicase has been characterized from Escherichia coli and Mycobacterium tuberculosis [36–38] and it is a critical component of the DNA repair process of prokaryotes. In particular, UvrD is required for the mismatch repair (MMR) and nucleotide excision repair (NER) to repair mismatches occurring during replication or DNA lesions such as UV-induced pyrimidine dimers or more bulky adducts [35, 39, 40]. In a recent study we have reported the detailed biochemical characterization of the UvrD helicase from P. falciparum and have shown that it exhibits the ssDNA-dependent ATPase activity and the DNA helicase activity in 3’ to 5’ direction [32, 33, 35]. Recent study on UvrD in different Plasmodium species revealed that the other species of Plasmodium also contain putative UvrD helicase .
Here, in the follow up study of our previous work , we report the effect of different DNA interacting compounds (actinomycin, camptothecin, ciprofloxacin, cisplatin, cyclophosphamide, DAPI, daunorubicin, etoposide, ethidium bromide, genistein, morin, netropsin, nogalamycin and novobiocin) on the helicase and ATPase activities of PfUvrD helicase. Out of all these molecules tested, only daunorubicin, ethidium bromide, netropsin, and nogalamycin were found to be potent inhibitors for the PfUDN enzymatic activities. The inhibition of PfUvrD by dsRNA showed that it is required for the ex-vivo intraerythrocytic development of the parasite P. falciparum 3D7. This study will set the stage for designing the specific inhibitors for inhibiting the enzymatic activity of PfUDN which in turn will block the parasite growth as well.
Nucleoside triphosphates and deoxynucleoside triphosphates were obtained from Pharmacia (Uppsala, Sweden) and [γ-32P] ATP was purchased from Perkin Elmer (Boston, MA, USA). M13mp19 ssDNA was purchased from Invitrogen (Carlsbad, CA, USA). Synthetic DNA oligonucleotides were synthesized chemically. The DNA-interacting compounds, camptothecin, ciprofloxacin, cisplatin, DAPI, daunorubicin, etoposide and morin were purchased from Topogene Inc. (Columbus, OH, USA). Cyclophosphamide, genistein, netropsin, nogalamycin and novobiocin were obtained from Sigma Chemical Co. (St Louis, MO, USA), ethidium bromide and actinomycin was obtained from BDH (E. Merck, Mumbai, India) and Boehringer Mannheim (Indianapolis, IN, USA), respectively. All of these compounds were dissolved in dimethylsulfoxide (DMSO) and stored at 4°C in the dark.
DNA dependent ATPase assay
Standard protocol of ATPase assay was followed as described in the previous report [32, 41]. The hydrolysis of ATP catalyzed by PfUDN was assayed by measuring the formation of Pi from [γ-32P] ATP. The reaction mixture of 10 μl contained [γ-32P] ATP (specific activity 222 TBq.mmol-1) and cold ATP (1 mM), ATPase buffer (20 mM Tris-HCl, pH 8.0, 8 mM DTT, 1.0 mM MgCl2, 20 mM KCl and 16 μg/ml BSA), purified PfUDN and 50 ng or 100 ng of M13 mp19 ssDNA. The reaction mixtures were incubated at 37°C for 60 min. This was followed by thin layer chromatography (TLC), and the quantitation was done using Alpha Imager-EP/Image-J software ( http://rsbweb.nih.gov/ij/). In order to study the effect of various compounds on ssDNA-dependent ATPase activity, different compounds were added into the reaction mixture prior to the addition of the PfUDN. In another set of experiment, PfUDN was pre-incubated (15 min) with these compounds in order to obtain the insight of inhibitory mechanism. All the experiments were performed at least two times and quantification data was used to calculate the standard deviation using Microsoft Excel 2010 and mean value was used to prepare the graph.
Preparation of substrate and DNA helicase assay
Helicase assay was demonstrated using the purified fraction of PfUDN. The specially designed partial duplex substrate consisted of a 32P-labelled 47-mer DNA oligodeoxynucleotide annealed to M13mp19 phage ssDNA. This oligodeoxynucleotide of the nucleotide sequence 5'- (T)15GTTTTCCCAGTCACGAC(T)15-3' contains 15 base-pairs of non-complementary region (T)15 at both the 5’ and 3’ ends. Oligodeoxynucleotide was labeled at 5′-end with T4 polynucleotide kinase (PNK) (5U) (New England Biolabs) and 1.85 MBq of [γ-32P] ATP (specific activity 222 TBq/mmol) at 37°C for one hour and then annealed using standard annealing buffer (20 mM Tris-HCl, pH 7.5, 10 mM MgCl2, 100 mM NaCl, 1 mM DTT) with 0.5 μg of single-stranded circular M13mp19 (+) phage DNA by heating at 95°C for 1 min and then transferring immediately to 65°C for 2 min and then slow cooling to room temperature. Using gel filtration through a Sepharose 4B column (Pharmacia, Sweden) the non-hybridized oligodeoxynucleotide was removed . The reaction volume of 10 μl containing the 32P-labeled helicase substrate (1000 cpm/10 μl) in appropriate buffer (20 mMTris-HCl, pH 8.0, 8 mM DTT, 1.0 mM MgCl2, 20 mMKCl and 16 μg/ml BSA) and PfUDN was incubated at 37°C for 60 min. The substrate and products were separated by electrophoresis on a nondenaturing 12% PAGE and the gel was exposed to hyper film for autoradiography or scanned on phosphoimager. In order to study the effect of DNA-interacting compounds on helicase activity, different compounds were added to the helicase reaction mixture prior to the addition of the PfUDN helicase. All the experiments were performed in duplicate and quantitation of both the substrate and unwound DNA bands was done using AlphaImager-EP/Image-J software ( http://rsbweb.nih.gov/ij/). Quantification data was used to calculate the standard deviation using Microsoft Excel 2010 and mean value was used to prepare the graph.
Double stranded (ds) RNA preparation
The clone of PfUDN in the pGEMT easy vector of Promega (Madison, WI, USA) was used as a template to amplify the gene, using T7 and SP6 primers . Similarly the clone of GFP into pGEMT easy vector was used as control. The PCR products using these two primers were purified using the Wizard DNA clean-up system from Promega. These purified templates were used for in vitro transcription to generate sense RNA (sRNA) and anti-sense RNA (asRNA) using T7 and the SP6 RiboMAX Express large-scale RNA production system from Promega. For the production of dsRNA, equal amounts of sRNA and asRNA were mixed and incubated at 65°C for 30 min, and then the incubation was continued at room temperature overnight. The mixture was treated with DNase and precipitated after phenol/chloroform extraction. The pellet of dsRNA was dissolved in diethyl pyrocarbonate water and treated with RNase T1. These samples were checked on 1% (w⁄v) native agarose gel. This dsRNA was quantitated and used for the following experiments.
Parasite proliferation assay in presence of dsRNA targeted to UvrD helicase
For analyzing the effect of dsRNA, the cultures were adjusted to 4% hematocrit with 1% infected red blood cells (RBCs). 200 μl of this mixture was centrifuged at 1500xg in a Sorvall RT7 centrifuge (Du Pont, Newtown, CT, USA), and the pellet was resuspended in 50 μl of incomplete medium and 20 μg dsRNA per ml was added to this mixture. This mixture was incubated at 37°C with intermittent mixing to avoid settling of RBCs. After this incubation, serum was added to a final concentration of 20% and the mixture was dispensed in 96-well plates and incubated at 37°C for specific times. The smears were made at different intraerythrocytic developmental stage of the parasite and the effect was determined by microscopic examination as well as cyber green based assay . The parasite proliferation assay was performed in duplicate and quantification data (using ELISA reader) was used to calculate the standard deviation using Microsoft Excel 2010 and mean value was used to prepare the bar diagram.
Effect of various compounds on ssDNA-dependent ATPase activity
Comparison of inhibitory potential for ATPase activity
Effect of various compounds on DNA helicase activity of PfUDN
Comparison of inhibitory potential for helicase activity
Inhibition study of parasite growth by PfUDN ds-RNA
The identification of suitable drug target and newer class of antimalarial drugs has been a challenging task for the parasitologist worldwide. In order to consider a parasite protein as a drug target, it should be parasite specific and importantly essential for the parasite growth. In silico data revealed that parasite is unique with respect to the UvrD helicase as its human host lacks this essential enzyme. Furthermore, gene disruption or knockout study is required to firmly establish whether PfUvrD is essential for the malaria parasite growth. Interestingly PfUDN interaction with PfMLH, a crucial MMR protein, and their interplay to regulate each other activity points toward the importance of PfUvrD for the malaria parasite. On the basis of these observations, PfUvrD is expected as crucial helicase for the parasite’s intraerythrocytic developments and was proposed as suitable drug target to combat with dreaded infections of malaria parasite. dsRNA based inhibition study suggests that UvrD is an important enzyme and seems crucial for the successful nuclear division during early schizont stages of P. falciparum. Although, mechanism of action of dsRNA is not yet explored and has been controversial in these parasites [44–48].
In order to find the molecules which block the biochemical activities (ATP hydrolyzing and DNA unwinding activities) of PfUvrD, screening with various compounds including DNA interacting compounds was done in this study. The results of this study revealed that daunorubicin inhibited both ATPase and DNA unwinding or helicase activity of PfUDN with IC50 value of ~3 μM. Daunorubicin or daunomycin belongs to anthracycline family and is most commonly used as chemotherapeutic for the treatment specifically of acute myeloid leukemia and acute lymphocytic leukemia . Similar to the daunorubicin some other compounds like netropsin, nogalamycin and ethidium bromide also considerably inhibited the DNA dependent ATPase activity of PfUDN at low μM concentration. Previously, the effects of daunorubicin, netropsin and nogalamycin (50 μM) have been tested in the parasite culture (synchronized and unsynchronized) which showed considerable inhibition of parasite growth (~60-70% inhibition at 72 hour) . Similarly, ciprofloxacin has also been found effective for the inhibition of malaria parasite growth [50, 51]. Etoposide (VP16) which inhibits DNA unwinding activity of PfUDN, is clinically active against Kaposi’s sarcoma, testicular cancer, acute lymphocytic leukaemia and small-cell lung cancer . It was reviewed that effects of etoposide treatment on P. falciparum parasites showed enhanced cleavage of both nuclear and apicoplast and the induction of an apoptosis-like cell death process .
The inhibition of the ATPase activity with these compounds was prominent when DNA was preincubated with inhibitor molecule (Figure 1A versus Figure 1B). Thus the results indicate that possibly these compounds interfere with the binding of DNA with PfUDN protein, which ultimately leads to inhibition of DNA dependent ATP hydrolysis. Interestingly all these commercially available molecules, which have been found as inhibitor for the ATPase activity also inhibit the DNA helicase activity of PfUDN helicase. Thus this study further suggests that energy from the ATP hydrolysis is used as driving force for the DNA unwinding activity. Although, ciprofloxacin inhibited the helicase activity during screening at 20 μM concentration but it did not appreciably inhibit the activity at lower concentration (0.5-5 μM). Ciprofloxacin is a fluoroquinolone antibiotic, which moderately inhibited the ATPase as well as helicase activity of PfUDN helicase and it has also been reported to block the helicase activity of Mcm2-7 helicase . Interestingly, in the present study etoposide did not exhibit inhibition on the ATPase activity of PfUDN but significant inhibition of helicase activity was observed at 20 μM concentration. Similar to the ciprofloxacin, etoposide also failed to show appreciable inhibition of the helicase activity of PfUDN at lower concentration (0.5-5 μM).
Ethidium bromide is well known DNA intercalating compound thus it seems that after binding with DNA this compound blocks the interaction of PfUDN with DNA and inhibits the ATPase activity led helicase activity. Although, ethidium bromide cannot be used as drug because of its properties as potential mutagen but other inhibitors reported in the present study can be used as basic molecule to design and synthesize derivatives specific for the PfUvrD helicase. The concentration at which these compounds inhibit the ATPase and helicase activity of PfUDN is certainly not suitable for the therapeutics purpose but this study provides a basic idea to develop novel derivatives in order to achieve significant inhibition of ATPase and helicase activity of PfUvrD at much lower concentration. Thus this study will certainly help pharmacologists to develop derivative of these drugs specific to the PfUvrD which may result into significant inhibition at much lower concentration with the hope to be useful to fight with malaria. Furthermore the knockout out or gene disruption analysis of PfUvrD is required in order to establish the essentiality of UvrD for the parasite, P. falciparum but the results of present study with dsRNA targeted to N-terminal of UvrD at least indicates that PfUvrD is crucial for parasite and its growth is inhibited considerably during early schizont stages of asexual life cycle.
In previous studies we reported the detailed biochemical characterization of malaria parasite Plasmodium falciparum specific UvrD helicase . The biochemical studies revealed that PfUvrD exhibits the ATPase as well as DNA helicase activity. It unwinds DNA duplex in 3’-5’ direction and interacts with PfMLH to regulate each other biochemical activities . Recently, we have also reported that the genetically engineered synthetic UvrD helicase (appreciably shorter than native PfUvrD) also showed ATPase and helicase activity . In this study, we have identified daunorubicin, ethidium bromide, netropsin, and nogalamycin as potent inhibitors for the PfUDN enzymatic activities. The results further show that PfUvrD is crucial for the parasite survival as its dsRNA showed inhibition of intraerythrocytic development of the parasite P. falciparum 3D7 strain. This study strengthens the speculation that PfUvrD can serve as suitable drug target to control the malaria. Findings of this work can be used for designing the specific inhibitors for PfUvrD, which may result into specific inhibition of UvrD and in turn the parasite growth.
Double stranded RNA
Nucleotide excision repair
PfUvrD N terminal.
The authors sincerely thank Dr. Narendra Tuteja, Group Leader, Plant Molecular Biology group, ICGEB for valuable discussion and support. This work was supported by a grant from Department of Biotechnology, Government of India. Infra-structural support from the Department of Biotechnology, Government of India is gratefully acknowledged.
- Ahmad M, Tuteja R: Plasmodium falciparum RuvB proteins: emerging importance and expectations beyond cell cycle progression. Commun Integr Biol. 2012, 5 (4): 350-361. 10.4161/cib.20005.PubMedPubMed CentralView ArticleGoogle Scholar
- WHO: World-Malaria-Report. 2012, http://www.who.int/malaria/publications/world_malaria_report_2012/en/index.html ,Google Scholar
- Murray CJ, Rosenfeld LC, Lim SS, Andrews KG, Foreman KJ, Haring D, Fullman N, Naghavi M, Lozano R, Lopez AD: Global malaria mortality between 1980 and 2010: a systematic analysis. Lancet. 2012, 379 (9814): 413-431. 10.1016/S0140-6736(12)60034-8.PubMedView ArticleGoogle Scholar
- Zhang VM, Chavchich M, Waters NC: Targeting protein kinases in the malaria parasite: update of an antimalarial drug target. Curr Top Med Chem. 2012, 12 (5): 456-472. 10.2174/156802612799362922.PubMedView ArticleGoogle Scholar
- Bejon P, White MT, Olotu A, Bojang K, Lusingu JP, Salim N, Otsyula NN, Agnandji ST, Asante KP, Owusu-Agyei S, Abdulla S, Ghani AC: Efficacy of RTS,S malaria vaccines: individual-participant pooled analysis of phase 2 data. Lancet Infect Dis. 2013, 13 (4): 319-327. 10.1016/S1473-3099(13)70005-7.PubMedPubMed CentralView ArticleGoogle Scholar
- Vannice KS, Brown GV, Akanmori BD, Moorthy VS: MALVAC 2012 scientific forum: accelerating development of second-generation malaria vaccines. Malar J. 2012, 11: 372-10.1186/1475-2875-11-372.PubMedPubMed CentralView ArticleGoogle Scholar
- Mita T, Tanabe K: Evolution of Plasmodium falciparum drug resistance: implications for the development and containment of artemisinin resistance. Jpn J Infect Dis. 2012, 65 (6): 465-475. 10.7883/yoken.65.465.PubMedView ArticleGoogle Scholar
- Starzengruber P, Swoboda P, Fuehrer HP, Khan WA, Hofecker V, Siedl A, Fally M, Graf O, Teja-Isavadharm P, Haque R, Ringwald P, Noedl H: Current status of artemisinin-resistant falciparum malaria in South Asia: a randomized controlled artesunate monotherapy trial in Bangladesh. PLoS One. 2012, 7 (12): e52236-10.1371/journal.pone.0052236.PubMedPubMed CentralView ArticleGoogle Scholar
- Garcia-Bustos JF, Gamo FJ: Antimalarial drug resistance and early drug discovery. Curr Pharm Des. 2013, 19 (2): 270-281. 10.2174/138161213804070357.PubMedView ArticleGoogle Scholar
- Doerig C, Meijer L: Antimalarial drug discovery: targeting protein kinases. Expert Opin Ther Targets. 2007, 11 (3): 279-290. 10.1517/1472822.214.171.1249.PubMedView ArticleGoogle Scholar
- Canduri F, Perez PC, Caceres RA, De Azevedo WF: Protein kinases as targets for antiparasitic chemotherapy drugs. Curr Drug Targets. 2007, 8 (3): 389-398. 10.2174/138945007780058979.PubMedView ArticleGoogle Scholar
- Jirage D, Keenan SM, Waters NC: Exploring novel targets for antimalarial drug discovery: plasmodial protein kinases. Infect Disord Drug Targets. 2010, 10 (3): 134-146. 10.2174/187152610791163381.PubMedView ArticleGoogle Scholar
- Mpangase PT, Szolkiewicz MJ, Le Grange M, Smit JH, Burger PB, Joubert F: Discovery-2: an interactive resource for the rational selection and comparison of putative drug target proteins in malaria. Malar J. 2013, 12: 116-10.1186/1475-2875-12-116.PubMedPubMed CentralView ArticleGoogle Scholar
- Bullard KM, DeLisle RK, Keenan SM: Malarial kinases: novel targets for in silico approaches to drug discovery. Methods Mol Biol. 2013, 993: 205-229. 10.1007/978-1-62703-342-8_14.PubMedView ArticleGoogle Scholar
- Augagneur Y, Jaubert L, Schiavoni M, Pachikara N, Garg A, Usmani-Brown S, Wesolowski D, Zeller S, Ghosal A, Cornillot E, Said HM, Kumar P, Altman S, Ben Mamoun C: Identification and functional analysis of the primary pantothenate transporter, PfPAT, of the human malaria parasite Plasmodium falciparum. J Biol Chem. 2013, 288 (28): 20558-20567. 10.1074/jbc.M113.482992.PubMedPubMed CentralView ArticleGoogle Scholar
- Maloney P, Hedrick M, Peddibhotla S, Hershberger P, Milewski M, Gosalia P, Li L, Preuss J, Sugarman E, Hood B, Suyama E, Nguyen K, Vasile S, Sergienko E, Salanawil S, Stonich D, Su Y, Dahl R, Mangravita-Novo A, Vicchiarelli M, McAnally D, Smith LH, Roth G, Diwan J, Chung TDY, Pinkerton AB, Bode L, Becker K: A Selective Inhibitor of Plasmodium falciparum Glucose-6-Phosphate Dehydrogenase (PfG6PDH). 2011, U.S.A: Probe Reports from the NIH Molecular Libraries Program. National Center for Biotechnology InformationGoogle Scholar
- Ramdhave AS, Patel D, Ramya I, Nandave M, Kharkar PS: Targeting heat shock protein 90 for malaria. Mini Rev Med Chem. Bentham Science Publishers. U.S.A. 2013, 13 (13): 1903-1920. 10.2174/13895575113136660094.View ArticleGoogle Scholar
- Spitzmuller A, Mestres J: Prediction of the P. Falciparum target space relevant to malaria drug discovery. PLoS Comput Biol. 2013, 9 (10): e1003257-10.1371/journal.pcbi.1003257.PubMedPubMed CentralView ArticleGoogle Scholar
- Flannery EL, Chatterjee AK, Winzeler EA: Antimalarial drug discovery - approaches and progress towards new medicines. Nat Rev Microbiol. 2013, 11 (12): 849-862. 10.1038/nrmicro3138.PubMedPubMed CentralView ArticleGoogle Scholar
- Seow F, Sato S, Janssen CS, Riehle MO, Mukhopadhyay A, Phillips RS, Wilson RJ, Barrett MP: The plastidic DNA replication enzyme complex of Plasmodium falciparum. Mol Biochem Parasitol. 2005, 141 (2): 145-153. 10.1016/j.molbiopara.2005.02.002.PubMedView ArticleGoogle Scholar
- Tuteja R: Helicases - feasible antimalarial drug target for Plasmodium falciparum. Febs J. 2007, 274 (18): 4699-4704. 10.1111/j.1742-4658.2007.06000.x.PubMedView ArticleGoogle Scholar
- Tuteja R, Pradhan A: Unraveling the 'DEAD-box' helicases of Plasmodium falciparum. Gene. 2006, 376 (1): 1-12. 10.1016/j.gene.2006.03.007.PubMedView ArticleGoogle Scholar
- Xi XG: Helicases as antiviral and anticancer drug targets. Curr Med Chem. 2007, 14 (8): 883-915. 10.2174/092986707780362998.PubMedView ArticleGoogle Scholar
- Frick DN: Helicases as antiviral drug targets. Drug News Perspect. 2003, 16 (6): 355-362. 10.1358/dnp.2003.16.6.829307.PubMedPubMed CentralView ArticleGoogle Scholar
- Sharma S, Doherty KM, Brosh RM: DNA helicases as targets for anti-cancer drugs. Curr Med Chem Anticancer Agents. 2005, 5 (3): 183-199. 10.2174/1568011053765985.PubMedView ArticleGoogle Scholar
- Kwong AD, Rao BG, Jeang KT: Viral and cellular RNA helicases as antiviral targets. Nat Rev Drug Discov. 2005, 4 (10): 845-853. 10.1038/nrd1853.PubMedView ArticleGoogle Scholar
- Shadrick WR, Ndjomou J, Kolli R, Mukherjee S, Hanson AM, Frick DN: Discovering new medicines targeting helicases: challenges and recent progress. J Biomol Screen. 2013, 18 (7): 761-781. 10.1177/1087057113482586.PubMedPubMed CentralView ArticleGoogle Scholar
- Weller SK, Kuchta RD: The DNA helicase-primase complex as a target for herpes viral infection. Expert Opin Ther Targets. 2013, 17 (10): 1119-1132. 10.1517/14728222.2013.827663.PubMedPubMed CentralView ArticleGoogle Scholar
- Field HJ, Biswas S: Antiviral drug resistance and helicase-primase inhibitors of herpes simplex virus. Drug Resist Updat. 2011, 14 (1): 45-51. 10.1016/j.drup.2010.11.002.PubMedView ArticleGoogle Scholar
- Aggarwal M, Banerjee T, Sommers JA, Brosh RM: Targeting an Achilles' heel of cancer with a WRN helicase inhibitor. Cell Cycle. 2013, 12 (20): 3329-3335.PubMedPubMed CentralView ArticleGoogle Scholar
- Li B, Pai R, Di M, Aiello D, Barnes MH, Butler MM, Tashjian TF, Peet NP, Bowlin TL, Moir DT: Coumarin-based inhibitors of Bacillus anthracis and Staphylococcus aureus replicative DNA helicase: chemical optimization, biological evaluation, and antibacterial activities. J Med Chem. 2012, 55 (24): 10896-10908. 10.1021/jm300922h.PubMedPubMed CentralView ArticleGoogle Scholar
- Ahmad M, Ansari A, Tarique M, Satsangi AT, Tuteja R: Plasmodium falciparum UvrD helicase translocates in 3' to 5' direction, colocalizes with MLH and modulates its activity through physical interaction. PLoS One. 2012, 7 (11): e49385-10.1371/journal.pone.0049385.PubMedPubMed CentralView ArticleGoogle Scholar
- Tuteja R: In silico analysis of Plasmodium species specific UvrD helicase. Communicative and Integrative Biology. 2013, 6 (2): e23125-10.4161/cib.23125.PubMedPubMed CentralView ArticleGoogle Scholar
- Tuteja R: Genome wide identification of Plasmodium falciparum helicases: a comparison with human host. Cell Cycle. 2010, 9 (1): 104-120. 10.4161/cc.9.1.10241.PubMedView ArticleGoogle Scholar
- Shankar J, Tuteja R: UvrD helicase of Plasmodium falciparum. Gene. 2008, 410 (2): 223-233. 10.1016/j.gene.2007.12.015.PubMedView ArticleGoogle Scholar
- Matson SW, Robertson AB: The UvrD helicase and its modulation by the mismatch repair protein MutL. Nucleic Acids Res. 2006, 34 (15): 4089-4097. 10.1093/nar/gkl450.PubMedPubMed CentralView ArticleGoogle Scholar
- Sinha KM, Stephanou NC, Gao F, Glickman MS, Shuman S: Mycobacterial UvrD1 is a Ku-dependent DNA helicase that plays a role in multiple DNA repair events, including double-strand break repair. J Biol Chem. 2007, 282 (20): 15114-15125. 10.1074/jbc.M701167200.PubMedView ArticleGoogle Scholar
- Sinha KM, Stephanou NC, Unciuleac MC, Glickman MS, Shuman S: Domain requirements for DNA unwinding by mycobacterial UvrD2, an essential DNA helicase. Biochemistry. 2008, 47 (36): 9355-9364. 10.1021/bi800725q.PubMedPubMed CentralView ArticleGoogle Scholar
- Yamaguchi M, Dao V, Modrich P: MutS and MutL activate DNA helicase II in a mismatch-dependent manner. J Biol Chem. 1998, 273 (15): 9197-9201. 10.1074/jbc.273.15.9197.PubMedView ArticleGoogle Scholar
- Schaaper RM: Base selection, proofreading, and mismatch repair during DNA replication in Escherichia coli. J Biol Chem. 1993, 268 (32): 23762-23765.PubMedGoogle Scholar
- Ahmad M, Tuteja R: Plasmodium falciparum RuvB2 translocates in 5'-3' direction, relocalizes during schizont stage and its enzymatic activities are up regulated by RuvB3 of the same complex. Biochim Biophys Acta. 2013, 1834 (12): 2795-2811. 10.1016/j.bbapap.2013.10.010.PubMedView ArticleGoogle Scholar
- Pradhan A, Tuteja R: Plasmodium falciparum DNA helicase 60. dsRNA- and antibody-mediated inhibition of malaria parasite growth and downregulation of its enzyme activities by DNA-interacting compounds. Febs J. 2006, 273 (15): 3545-3556. 10.1111/j.1742-4658.2006.05362.x.PubMedView ArticleGoogle Scholar
- Panchal M, Rawat K, Kumar G, Kibria KM, Singh S, Kalamuddin M, Mohmmed A, Malhotra P, Tuteja R: Plasmodium falciparum signal recognition particle components and anti-parasitic effect of ivermectin in blocking nucleo-cytoplasmic shuttling of SRP. Cell Death Dis. 2014, 5: e994-10.1038/cddis.2013.521.PubMedPubMed CentralView ArticleGoogle Scholar
- Sriwilaijaroen N, Boonma S, Attasart P, Pothikasikorn J, Panyim S, Noonpakdee W: Inhibition of Plasmodium falciparum proliferation in vitro by double-stranded RNA directed against malaria histone deacetylase. Biochem Biophys Res Commun. 2009, 381 (2): 144-147. 10.1016/j.bbrc.2009.01.165.PubMedView ArticleGoogle Scholar
- Malhotra P, Dasaradhi PV, Kumar A, Mohmmed A, Agrawal N, Bhatnagar RK, Chauhan VS: Double-stranded RNA-mediated gene silencing of cysteine proteases (falcipain-1 and -2) of Plasmodium falciparum. Mol Microbiol. 2002, 45 (5): 1245-1254. 10.1046/j.1365-2958.2002.03105.x.PubMedView ArticleGoogle Scholar
- Pradhan A, Tuteja R: Bipolar, dual Plasmodium falciparum helicase 45 expressed in the intraerythrocytic developmental cycle is required for parasite growth. J Mol Biol. 2007, 373 (2): 268-281. 10.1016/j.jmb.2007.07.056.PubMedView ArticleGoogle Scholar
- Baum J, Papenfuss AT, Mair GR, Janse CJ, Vlachou D, Waters AP, Cowman AF, Crabb BS, De Koning-Ward TF: Molecular genetics and comparative genomics reveal RNAi is not functional in malaria parasites. Nucleic Acids Res. 2009, 37 (11): 3788-3798. 10.1093/nar/gkp239.PubMedPubMed CentralView ArticleGoogle Scholar
- Mueller AK, Hammerschmidt-Kamper C, Kaiser A: RNAi in Plasmodium. Curr Pharm Des. 2013, 20 (2): 278-283.View ArticleGoogle Scholar
- Tan C, Tasaka H, Yu KP, Murphy ML, Karnofsky DA: Daunomycin, an antitumor antibiotic, in the treatment of neoplastic disease. Clinical evaluation with special reference to childhood leukemia. Cancer. 1967, 20 (3): 333-353.PubMedGoogle Scholar
- Divo AA, Sartorelli AC, Patton CL, Bia FJ: Activity of fluoroquinolone antibiotics against Plasmodium falciparum in vitro. Antimicrob Agents Chemother. 1988, 32 (8): 1182-1186. 10.1128/AAC.32.8.1182.PubMedPubMed CentralView ArticleGoogle Scholar
- Dahl EL, Rosenthal PJ: Multiple antibiotics exert delayed effects against the Plasmodium falciparum apicoplast. Antimicrob Agents Chemother. 2007, 51 (10): 3485-3490. 10.1128/AAC.00527-07.PubMedPubMed CentralView ArticleGoogle Scholar
- Garcia-Estrada C, Prada CF, Fernandez-Rubio C, Rojo-Vazquez F, Balana-Fouce R: DNA topoisomerases in apicomplexan parasites: promising targets for drug discovery. Proc Biol Sci. 2010, 277 (1689): 1777-1787. 10.1098/rspb.2009.2176.PubMedPubMed CentralView ArticleGoogle Scholar
- Simon N, Bochman ML, Seguin S, Brodsky JL, Seibel WL, Schwacha A: Ciprofloxacin is an inhibitor of the Mcm2-7 Replicative Helicase. Biosci Rep. 2013, 33 (5): e00072-PubMedPubMed CentralView ArticleGoogle Scholar
- Ansari A, Tarique M, Tuteja R: Genetically engineered synthetic miniaturized versions of Plasmodium falciparum UvrD helicase Are catalytically active. PLoS One. 2014, 9 (3): e90951-10.1371/journal.pone.0090951.PubMedPubMed CentralView ArticleGoogle Scholar
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