Iments in duplicates with two different amounts of protein (0.2 and 0.8 ug

Iments in duplicates with two different amounts of protein (0.2 and 0.8 ug). Results derived from two different amounts of protein are almost identical. Only results from 0.2 ug were presented in this study.Generation of Infectious HCVcc and Infectivity AssayInfectious HCV particles (HCVcc) were obtained as described previously [16,17,18]. To generate infectious HCVcc, in vitrotranscribed genomic J6/JFH RNA was delivered into HuH7.5 cells by electroporation. The HCVcc was recovered from cell culture medium after passage for 2 weeks. The virus-containing supernatant was clarified by low-speed centrifugation, passed Biotin-NHS web through a filter with the pore size of 0.45 mm, and concentrated by ultracentrifugation. For the infectivity assay, HuH7.5 cells were separated into 3.5 cm Petri dish at the density of 26105 cells. After 4 hrs, the cells were attached and 100 ml of HCVcc-containing supernatant (MOI = 0.1) was added to each dish and incubated for additional 72 hrs. The mock- and HCV-infected cell lysates were then harvested for Western blot assay to detect protein expression and for the analysis to detect 59 (39)-deoxyribonucleotidase activity.More than 50 of the 59(39)-deoxyribonucleotidase Activity in the HuH7 Cells is from the cdN ProteinTo evaluate the effect of HCV on the enzymatic activity of cdN, the 59(39)-deoxyribonucleotidase activity assay to detect the dephosphorylation of dUMP was established following a published procedure [15]. To confirm whether this assay could indeed measure cdN activity, cdN protein was over-expressed exogenously in HuH7 cells as a gain-of-function control. As expected, 59(39)deoxyribonucleotidase activity increased about 2 fold in these cdN protein over-expressed cells (Fig. 4A). To further confirm the accuracy of this assay, shRNAs targeting cdN gene were used as a loss-of-function control. Comparing the control shRNA targeting the luciferase gene, the cdN shRNA reduced the 59(39)-deoxyribonucleotidase activity significantly (Fig. 4B). Thus, the 59(39)-HCV NS3 Interacts with cdN ProteinFigure 3. Confocal microscopy analysis of HCV NS3 and cdN proteins in cultured cells. (A) HuH7 cells were co-transfected with the plasmid expressing the cdN protein with a V5 tag and the plasmid expressing HCV NS3/4A protein with a myc tag. After transfection, the cells were fixed and initially stained with mouse anti-myc and Cy3-conjugated anti-mouse antibodies. FITC-conjugated anti-V5 antibodies were then used for staining. (B) HCV subgenomic RNA replicon cells were fixed and stained with mouse anti-NS3 and goat anti-cdN, followed by Cy3-conjugated antimouse IgG and FITC-conjugated anti-goat IgG antibodies. Green represents cdN protein; red represents HCV NS3; blue represents nucleus staining with DAPI; the orange color in merged image indicated colocalization of cdN and HCV NS3 proteins. doi:10.1371/journal.pone.0068736.gdeoxyribonucleotidase activity assay used in this study could indeed measure the cdN activity. cdN and mdN (mitochondrial 59(39)-deoxyribonucleotidase; dNT-2) catalyze the dephosphorylation of deoxyribonucleoside monophosphates and regulate dTTP formation in cytosol and mitochondria respectively, protecting DNA replication from imbalanced precursor pools [19,20,21,22]. The assay analyzing the dUMP dephosphorylation measures both cdN and mdN activities [15]. To Fruquintinib chemical information determine the individual contribution of these two proteins in the analysis, shRNA knockdown experiments were performed. When cdN expression was re.Iments in duplicates with two different amounts of protein (0.2 and 0.8 ug). Results derived from two different amounts of protein are almost identical. Only results from 0.2 ug were presented in this study.Generation of Infectious HCVcc and Infectivity AssayInfectious HCV particles (HCVcc) were obtained as described previously [16,17,18]. To generate infectious HCVcc, in vitrotranscribed genomic J6/JFH RNA was delivered into HuH7.5 cells by electroporation. The HCVcc was recovered from cell culture medium after passage for 2 weeks. The virus-containing supernatant was clarified by low-speed centrifugation, passed through a filter with the pore size of 0.45 mm, and concentrated by ultracentrifugation. For the infectivity assay, HuH7.5 cells were separated into 3.5 cm Petri dish at the density of 26105 cells. After 4 hrs, the cells were attached and 100 ml of HCVcc-containing supernatant (MOI = 0.1) was added to each dish and incubated for additional 72 hrs. The mock- and HCV-infected cell lysates were then harvested for Western blot assay to detect protein expression and for the analysis to detect 59 (39)-deoxyribonucleotidase activity.More than 50 of the 59(39)-deoxyribonucleotidase Activity in the HuH7 Cells is from the cdN ProteinTo evaluate the effect of HCV on the enzymatic activity of cdN, the 59(39)-deoxyribonucleotidase activity assay to detect the dephosphorylation of dUMP was established following a published procedure [15]. To confirm whether this assay could indeed measure cdN activity, cdN protein was over-expressed exogenously in HuH7 cells as a gain-of-function control. As expected, 59(39)deoxyribonucleotidase activity increased about 2 fold in these cdN protein over-expressed cells (Fig. 4A). To further confirm the accuracy of this assay, shRNAs targeting cdN gene were used as a loss-of-function control. Comparing the control shRNA targeting the luciferase gene, the cdN shRNA reduced the 59(39)-deoxyribonucleotidase activity significantly (Fig. 4B). Thus, the 59(39)-HCV NS3 Interacts with cdN ProteinFigure 3. Confocal microscopy analysis of HCV NS3 and cdN proteins in cultured cells. (A) HuH7 cells were co-transfected with the plasmid expressing the cdN protein with a V5 tag and the plasmid expressing HCV NS3/4A protein with a myc tag. After transfection, the cells were fixed and initially stained with mouse anti-myc and Cy3-conjugated anti-mouse antibodies. FITC-conjugated anti-V5 antibodies were then used for staining. (B) HCV subgenomic RNA replicon cells were fixed and stained with mouse anti-NS3 and goat anti-cdN, followed by Cy3-conjugated antimouse IgG and FITC-conjugated anti-goat IgG antibodies. Green represents cdN protein; red represents HCV NS3; blue represents nucleus staining with DAPI; the orange color in merged image indicated colocalization of cdN and HCV NS3 proteins. doi:10.1371/journal.pone.0068736.gdeoxyribonucleotidase activity assay used in this study could indeed measure the cdN activity. cdN and mdN (mitochondrial 59(39)-deoxyribonucleotidase; dNT-2) catalyze the dephosphorylation of deoxyribonucleoside monophosphates and regulate dTTP formation in cytosol and mitochondria respectively, protecting DNA replication from imbalanced precursor pools [19,20,21,22]. The assay analyzing the dUMP dephosphorylation measures both cdN and mdN activities [15]. To determine the individual contribution of these two proteins in the analysis, shRNA knockdown experiments were performed. When cdN expression was re.