Development of a luciferase-based biosensor to assess enterovirus 71 3C protease activity in living cells

Enterovirus 71 (EV71) is a major pathogen of hand, foot, and mouth disease (HFMD). To date, no antiviral drug has been approved to treat EV71 infection. Due to the essential role that EV71 3 C protease (3Cpro) plays in the viral life cycle, it is generally considered as a highly appealing target for antiviral drug development. In this study, we present a transgene-encoded biosensor that can accurately, sensitively and quantitatively report the proteolytic activity of EV71 3Cpro. This biosensor is based on the catalyzed activity of a pro–interleukin (IL)-1β-enterovirus 3Cpro cleavage site-Gaussia Luciferase (GLuc) fusion protein that we named i-3CS-GLuc. GLuc enzyme is inactive in the fusion protein because of aggregation caused by pro–IL-1β. However, the 3Cpro of EV71 and other enteroviruses, such as coxsackievirus A9 (CVA9), coxsackievirus B3 (CVB3), and poliovirus can recognize and process the canonical enterovirus 3Cpro cleavage site between pro–IL-1β and GLuc, thereby releasing and activating GLuc and resulting in increased luciferase activity. The high sensitivity, ease of use, and applicability as a transgene in cell-based assays of i-3CS-GLuc biosensor make it a powerful tool for studying viral protease proteolytic events in living cells and for achieving high-throughput screening of antiviral agents.

with a luminometer, providing the detection sensitivity up to femtogram level 18 . Gaussia Luciferase (GLuc) is a naturally secreted luciferase from the deep sea copepod Gaussia Princeps 19 . Deletion of the N-terminal secretion signal peptide of GLuc made it intracellularly retained but did not affect its catalytic activity 20 . In 2013, scientists found that the fusion of mouse pro-interleukin (IL)-1β on the N-terminal of GLuc lacking its secretion signal peptide can inhibit its catalytic activity because pro-IL-1β possesses a strong propensity to form protein aggregates, and based on this, they developed a biosensor pro-IL-1β-GLuc (iGLuc) that can report the proteolytic activity of caspase-1 in the course of inflammasome activation in a highly sensitive manner 21 .
In this study, we report a quantifiable and sensitive transgene-encoded biosensor that monitors the activity of EV71 3C pro in living cells. As shown in Fig. 1, a canonical enterovirus 3C pro cleavage site EALFQ↓GPPK was inserted between mouse pro-IL-1β and GLuc lacking its secretion signal peptide to generate the biosensor pro-IL-1β-enterovirus 3C pro cleavage site-GLuc (i-3CS-GLuc). Within this biosensor, the GLuc enzyme is normally inactive because of the protein aggregation caused by pro-IL-1β. We demonstrated that the 3C pro of EV71 and some other enteroviruses could recognize and process the EALFQ↓GPPK site within i-3CS-GLuc, thus activating the GLuc enzyme and allowing the monitoring of cytosolic cleavage events and protease activity with high sensitivity and specificity. Moreover, this biosensor's ease of use and its applicability in living cells make it a powerful tool to screen antiviral drugs with high-throughput.

Construction and characterization of the Luc-based biosensor i-3CS-GLuc for EV71 3C pro activity.
As shown in Fig. 2A, a fusion protein construct of mouse pro-IL-1β and GLuc lacking its N-terminal secretion signal (iGLuc) was generated as described in a previous report 21 to serve as the negative control in this study. To generate biosensors for EV71 3C pro activity, the canonical enterovirus 3C pro cleavage site EALFQ↓GPPK was inserted into the iGLuc construct at different positions. We replaced the caspase-1 cleavage site LVCD↓V within mouse pro-IL-1β with enterovirus 3C pro cleavage site EALFQ↓GPPK to generate the i-3CS-GLuc1 construct and inserted the EALFQ↓GPPK site between mouse pro-IL-1β and GLuc to generate the i-3CS-GLuc2 construct.
As shown in Figs 2B and S1, the co-expressed EV71 3C pro could recognize the EALFQ↓GPPK site in both biosensors. It cleaved i-3CS-GLuc1 to generate an approximately 38-kDa Flag tagged protein and cleaved i-3CS-GLuc2 to generate an approximately 21-kDa Flag tagged protein due to the different positions the EALFQ↓GPPK site inserted. In contrast, the negative control iGLuc, which included the caspase-1 cleavage site but did not include the 3C pro cleavage site, was cleaved by mouse caspase-1 but was not cleaved by 3C pro . These results indicated that EV71 3C pro could recognized and processed the EALFQ↓GPPK site within both i-3CS-GLuc biosensors effectively and specifically.
Luciferase assays were performed to validate the efficiency of our biosensors. As shown in Fig. 2C, with or without EV71 3C pro , the negative control iGLuc generated similar bioluminescence of (3.06 ± 0.05) × 10 5 and (3.20 ± 0.08) × 10 5 (N = 3) in HEK293T cells. In contrast, when we co-expressed EV71 3C pro with our biosensors, which led to the cleavage of fusion proteins, bioluminescence increased significantly. For i-3CS-GLuc1, the signal increased from (2.82 ± 0.31) × 10 5 to (7.04 ± 0.18) × 10 5 (N = 3) in the presence of EV71 3C pro . For i-3CS-GLuc2, a more significant increase of GLuc signal from (2.92 ± 0.06) × 10 5 to (25.71 ± 0.34) × 10 5 (N = 3) was measured. These results indicate that EV71 3C pro -mediated cleavage relieved the suppression of GLuc catalytic activity by pro-IL-1β in both biosensors. Thus, both biosensors can monitor the activity of EV71 3C pro . However, the i-3CS-GLuc2 construct showed a higher sensitivity and signal to background ratio (SBR). Because no identified conformation analysis result was available for full length mouse pro-IL-1β or GLuc, the conformation of i-3CS-GLuc constructs were predicted by I-TASSER server mainly based on homology to mature human IL-1β using default parameter [22][23][24] . As shown in the top predicted models (Fig. S2), the 3C pro cleavage site in i-3CS-GLuc2 is exposed on the surface, whereas the 3C pro cleavage site in i-3CS-Gluc1 is partially surrounded by other domains of i-3CS-Gluc1, which may prevent the access of 3C pro . Since the threading templates used for prediction has only 33% coverage of the full length of i-3CS-GLuc proteins, the quality of predicted models is low Figure 1. Working principle of the luciferase-based biosensor for EV71 3C pro activity. The biosensor i-3CS-GLuc consists of mouse pro-interleukin (IL)-1β, an EV71 3C protease cleavage site and Gaussia luciferase (GLuc) lacking N-terminal secretion signal peptide. In living cells, GLuc activity is suppressed by protein aggregation caused by pro-IL-1β. EV71 3C pro can recognize and process the cleavage site between pro-IL-1β and GLuc, thus releasing and activating the GLuc enzyme.
(C-score = −3.32 and −3.72, typically C-score is in the range of [−5, 2], a higher C-core implicates higher confidence of prediction). However, these predicted models indicated that the 3C pro cleavage site is more accessible in i-3CS-GLuc2 than in i-3CS-GLuc1, which may lead to greater cleavage and explain the increased sensitivity of i-3CS-GLuc2. Thus, i-3CS-GLuc2 was used for the subsequent experiments.
To confirm the specificity of our biosensor, a catalytically dead EV71 3C pro mutant H40D was used. H40 is an essential component of the catalytic triad of EV71 3C pro 25 . H40D substitution in the active site of EV71 3C pro disrupts its protease activity. Just as expected, the result of WBs showed that EV71 3C pro H40D could not cleave i-3CS-GLuc2 (Fig. 2D). As shown in Fig. 2E, the co-expression of EV71 3C pro with i-3CS-GLuc2 obviously increased bioluminescence, whereas the co-expression of EV71 3C pro H40D with i-3CS-GLuc2 minimally affected bioluminescence, indicating that catalytically inactive 3C pro is incapable of activating our biosensor and confirming that i-3CS-GLuc2 can monitor the proteolytic cleavage event precisely.
Monitoring the inhibition of EV71 3C pro activity by Rupintrivir using the i-3CS-GLuc2 biosensor.
Rupintrivir (AG7088) is a compound originally developed as an irreversible inhibitor of human rhinovirus (HRV) 3C pro 26 . In 2013, scientists found that Rupintrivir also functions as a high-affinity inhibitor of EV71 3C pro 27 . Thus, we used Rupintrivir to determine whether our biosensor could be used to measure the inhibition of EV71 3C pro . To test whether Rupintrivir is toxic to human embryonic kidney 293 T (HEK293T) cells, the Cell Counting Kit-8 (CCK-8) assay was performed. Rupintrivir at concentrations from 25 nM to 2 μM showed no obvious toxicity to HEK293T cells (Fig. 3A). In the absence of Rupintrivir, EV71 3 C pro cleaved and activated the biosensor i-3CS-GLuc2 to increase the GLuc signal from (4.07 ± 0.23) × 10 5 to (44.40 ± 4.49) × 10 5 (N = 3), with a SBR of 10.92 (Fig. 3C). However, upon treatment with 1 μM of Rupintrivir, EV71 3C pro only led to a slight increase in signal from (4.42 ± 0.58) × 10 5 to (5.16 ± 0.17) × 10 5 (N = 3), with an SBR of 1.17. This result was highly consistent (D) Cleavage of iGLuc and i-3CS-GLuc2 by wild-type EV71 3C pro and the catalytically inactive 3C pro mutant H40D detected by Western blotting assays. The blots of Anti-HA were cropped and the full-length blots were displayed in Supplementary Information. (E) Cleavage of iGLuc and i-3CS-GLuc2 by wild typed EV71 3C pro and the catalytically inactive 3C pro mutant H40D detected by luciferase assay. The results are presented as the means ± SD of triplicate measurements (Student's t test; ns, nonsignificant, ****p < 0.0001).
with Western blotting results (Fig. 3B), indicating that i-3CS-GLuc2 can accurately and sensitively monitor the inhibition event of EV71 3C pro activity by Rupintrivir.

Construction and characterization of an EV71 3C pro activity reporter cell line.
To facilitate antiviral drug screening, a HEK293T cell line that stably expresses i-3CS-GLuc2-Flag was constructed as described in the Methods section. Immunofluorescence assays were performed to assess protein expression. As shown in Fig. 4A, HEK293T and HEK293T-i-3CS-GLuc2 cells were immunostained with fluorescein isothiocyanate (FITC) labeled Flag antibodies. Because no endogenous Flag-tagged proteins are expressed in HEK293T cells, no FITC fluorescence was observed. In contrast, HEK293T-i-3CS-GLuc2 cells showed strong FITC fluorescence, indicating that i-3CS-GLuc2 expressed stably and effectively in this cell line.
To confirm this result, the cell line was transfected with the empty vector pCAGGS, pHA-3C, and pHA-H40D, and cells were harvested and subjected to Western blotting assays. As shown in Fig. 4B, the biosensor i-3CS-GLuc2 was strongly expressed and could be cleaved by EV71 3C pro in this cell line.
We next tested whether HEK293T-i-3CS-GLuc2 cells could be used to sensitively and accurately report EV71 3C pro activity. We seeded HEK293T-i-3CS-GLuc2 cells in 12-well plates and transfected them with 0-500 ng of p3C-HA to test the dose relationship of EV71 3C pro and Luc activity. As shown in Fig. 4C, a larger amount of EV71 3C pro leads to stronger bioluminescence as predicted, indicating that HEK293T-i-3CS-GLuc2 cells can be used to report the activity of EV71 3C pro in a quantitative manner.
We also tested the dose-dependent inhibition of EV71 3C pro activity by Rupintrivir using our reporter cell line. As shown in Fig. 4D, the background bioluminescence generated by HEK293T-i-3CS-GLuc2 cells was not affected by the concentration of Rupintrivir. However, when EV71 3C pro was expressed in the reporter cell line, the resulting bioluminescence increased to (38.28 ± 0.09) × 10 5 and then decreased to (5.07 ± 0.04) × 10 5 (N = 3) as the Rupintrivir concentration was increased from 0 nM to 200 nM.
To test whether EV71 infection will activate the biosensor within HEK293T-i3CS-GLuc2 cells, these cells were infected with an EV71 BrCr-TR strain at a multiplicity of infection (MOI) of 0-5. As shown in Fig. 4E, there was a good correlation between viral MOI and the bioluminescence produced by GLuc, indicating that the reporter cell line can be used to monitor EV71 infection.

Optimization and validation of HEK293T-i-3CS-GLuc2 based antiviral drugs screening system.
To develop a HEK293T-i-3CS-GLuc2 based antiviral drugs screening system, we first identified the appropriate MOI for viral infection. HEK293T-i-3CS-GLuc2 cells infected with the EV71 BrCr-TR strain at an MOI of 2.5 or 5 produced strong GLuc signals (Fig. 4E) and evident cytopathic effect (CPE) without detachment. Therefore, we selected an MOI of 4 in the following experiments.
We next used Rupintrivir to determine whether HEK293T-i-3CS-GLuc2 cells could be used as an anti-EV71 drug screening system. The reported half maximal inhibitory concentration (IC 50 ) of Rupintrivir against the EV71 695 F strain (MOI = 0.1) is 14 nM in RD cells 27 . In this study, we examined the inhibitory effects of Rupintrivir at different concentrations against the EV71 BrCr-TR strain in our reporter cell line using Luc assays, the 50% tissue culture infectious dose (TCID 50 ) assays, CPE observation, WB assays and quantitative reverse transcription PCR (RT-qPCR).
The results of Luc assays were shown in Fig. 5A, the resulting bioluminescence of HEK293T-i-3CS-GLuc2 cells increased from (1.85 ± 0.04) × 10 5 to (13.66 ± 0.09) × 10 5 (N = 3) upon infection with the EV71 BrCr-TR strain and decreased to (1.78 ± 0.05) × 10 5 (N = 3) as the Rupintrivir concentration increased from 0 nM to 200 nM, indicating the excellent anti-EV71 effect of Rupintrivir. Consistent with this result, the TCID 50 value also decreased with an increasing Rupintrivir concentration in a dose-dependent manner (Fig. 5B). To further assess the anti-EV71 effects of Rupintrivir, we tested the expression of the viral structure protein VP1 with WBs. As shown in Fig. 5C, Rupintrivir treatment decreased the expression level of the VP1 protein in a dose-dependent  manner. Furthermore, we tested the VP1 mRNA level using RT-qPCR. When treated with 200 nM Rupintrivir, the VP1 mRNA was only (0.31 ± 0.04)% (N = 5) of the level with no Rupintrivir treatment. As shown in Fig. 5E, the reporter cell line infected with the EV71 BrCr-TR strain presented evident CPEs 24 hours after infection. However, the cell morphology gradually returned to normal as the concentration of Rupintrivir was increased. The IC 50 of Rupintrivir against the EV71 BrCr-TR strain on our reporter cell line was estimated to be around The results are presented as the means ± SD of triplicate measurements (Student's t test; ns, nonsignificant, *p < 0.05, ***p < 0.001, ****p < 0.0001). (B) Dose effect of Rupintrivir on viral titer detected by the TCID 50 assay. The results are presented as the means ± SD of triplicate measurements (Student's t test; **p < 0.01, ***p < 0.001, ****p < 0.0001). (C) The expression level of EV71 VP1 protein detected by Western blotting assays. The blots were cropped and the full-length blots were displayed in Supplementary Information. (D) Dose effect of Rupintrivir on the EV71 VP1 mRNA level detected by RT-qPCR. The results are presented as means ± SD of five measurements (Student's t test; ***p < 0.001, ****p < 0.0001). (E) CPEs of EV71-infected cells treated with and without Rupintrivir at various concentration. Scale bar: 300 μm. (F) The data of a highthroughput assay using HEK293T-i3CS-GLuc2 cells accessing the inhibition effects of Rupintrivir. 1 × 10 5 HEK293T-i-3CS-GLuc2 cells seeded in 96-well assay plates were infected with the EV71 BrCr-TR strain at an MOI of 4, and treated with 100 nM of Rupintrivir (Rupintrivir+) or methanol (Rupintrivir−). Bioluminescence was measured at 24 hours post infection.
12.5 nM based on these assays. The consistency of these experiments indicates that HEK293T-i-3CS-GLuc2 cells could be applied as an antiviral drug screening tool.
To validate whether HEK293T-i-3CS-GLuc2 cells could be used for high-throughput screening (HTS), the value of Z factor was determined. HEK293T-i-3CS-GLuc2 cells seeded in 96-well assay plates were infected with the EV71 BrCr-TR strain at an MOI of 4, then treated with Rupintrivir at 100 nM or with methanol as negative control. The assay data of representative samples were shown in Fig. 5F. According to the formula described in the previous research 28 , Z factor was calculated to be 0.62, indicating our system could provide excellent HTS assays (1 > Z > 0.5) 28 . 29 and was used to validate an EV71 3C pro -dependent bioluminescence imaging assay for anti-viral screening in a previous study 30 . Herein, GW5074 was selected to further validate the efficiency of HEK293T-i-3CS-GLuc2 cells for screening anti-EV71 agents. First, the cytotoxicity of GW5074 on HEK293T cells was tested using CCK-8 assays. Treatment with GW5074 up to 20 μM showed no significant influence on cell viability (Fig. S3). To assess the anti-EV71 effects of GW5074, HEK293T-i-3CS-GLuc2 cells were infected with the EV71 BrCr-TR strain at an MOI of 4 and treated with different concentrations (0, 2.5, 5, 10 and 20 μM) of GW5074. As shown in Fig. S4, obvious CPEs were observed at 24 h post infection without GW5074 treatment, whereas the CPEs in the cells treated with GW5074 were inhibited in a dose-dependent manner. To assess the anti-EV71 effect of GW5074 using the i-3CS-GLuc2 biosensor, GLuc bioluminescence was measured 24 hours after infection. As shown in Fig. 6A, treatment with GW5074 significantly decreased the resulting bioluminescence in a dose-dependent manner. Additionally, WB assays showed that GW5074 treatment decreased EV71 VP1 expression (Fig. 5B) and RT-qPCR assay showed that GW5074 treatment decreased the EV71 VP1 mRNA level (Fig. 5C). The viral TCID 50 was also decreased by GW5074 in a dose-dependent manner (Fig. 5D). The consistency of these experiments further indicates that HEK293T-i-3CS-GLuc2 cells could be used for antiviral drugs screening. In the Enterovirus family, some viruses share the same 3C pro cleavage site. Thus theoretically, the i-3CS-GLuc biosensor could be used for some other enteroviruses whose 3C pro can recognize the EALFQ↓GPPK site. To test this possibility, the CVA9 Griggs strain, the CVB3 Nancy strain and the poliovirus vaccine strain Sabin 3 were used to infect HEK293T-i-3CS-GLuc2 cells at an MOI of 0.5. At 24 hours post infection, cells were harvested and subjected to luciferase assays. As shown in Fig. 7, all three viruses activated GLuc and increased bioluminescence. The SBRs of CVA9, CVB3, and poliovirus infection were 3.60, 3.36 and 4.45 (three replicates each), indicating that the biosensor is also effective for mearing 3 C pro activity in other viruses of the Enterovirus family.

Discussion
Considering the continual outbreaks and serious clinical manifestations of children and infants caused by EV71, the prevention and treatment of this virus are urgently desired. In this study, we developed and evaluated a Luc-based biosensor for viral protease activity. We demonstrated that EV71 3 C pro can cleave and activate i-3CS-GLuc biosensor and thus report the 3C pro activity in a quantitative manner.
Various viral protease activity reporter systems have been developed, most are based on in vitro purified enzymes and their substrates, and use different detection technologies such as the fluorescence resonance energy transfer (FRET) 31 . Briefly, peptides bearing protease cleavage sites and FRET donor-receptor pairs were used as substrates for in vitro purified proteases to analysis their activity. FRET signals were activated when cleavage of peptides separated the fluorescent donor from the acceptor. This strategy has been applied to multiple viral proteases for inhibitor screening, including NS2B-NS3 of West Nile Virus 32 and 3C or 3C-like protease of Picornaviruses, Noroviruses, and Coronaviruses 33 . However, in vitro assays are often unable to reliably reflect the actual cleavage events that occur in complex milieus such as living cells and animals. In this study, both the biosensor and the reporter cell line allowed the monitoring of viral protease activity in living cells instead of in vitro. Numerous reports have demonstrated that the GLuc reporter can be used in small animal models as a marker to monitor different in vivo biological events such as tumor growth and proliferation, viral infection and replication as well as cell circulation [34][35][36] . Thus theoretically, our biosensor could also be used in animal models to monitor viral protease activity.
Compared with Western blotting and various enzymatic activity assays, Luc assays are highly sensitive and extremely easy to perform, requiring only minutes to accomplish. The ease of use and applicability as a transgene in cell-based assays of our biosensor render it a powerful tool to study viral protease cleavage events and screen antiviral drugs with high-throughput. In this study, we transduced the biosensor i-3CS-GLuc2 into HEK293T cells to generate a reporter cell line and verified that this cell line could be applied as a high-throughput antiviral screening tool. This biosensor could also be transduced into other cell types to generate additional reporter cell lines and monitor viral protease activity in various cells including all types of nerve cells.
Moreover, in addition to enteroviruses including EV71, CVA9, CVB3, and poliovirus, by changing the cleavage site, this reporter could also be used to detect the protease activity of other viruses. However, some restrictions should be taken into consideration when it was applied to other viral proteases. The sensor protein should be expressed in the same intracellular location with the viral protease to ensure it could be cleaved to generated active GLuc. In our case, both proteins were expressed in the cytosol. But some viral proteases may localize to different subcellular structures, for example, dengue virus NS2B-NS3 is bound to the ER membrane. The lack of physical interaction would make the protease activity detection impossible.
In summary, we have established a Luc-based biosensor for EV71 3C pro activity and developed a high-throughput antiviral agent screening system on the basis of this biosensor. This system is highly sensitive, easily operated and accurately quantifiable, providing a powerful tool for monitoring viral protease activity and for performing the high-throughput screening of antiviral drugs in living cells. In theory, this biosensor could be expanded to other proteases of many other type of viruses, and be applied in animal models. Therefore, this biosensor should be extremely useful for studying viral proteases and screening novel antiviral agents.

Cells and viruses. HEK293T cells and African green monkey kidney epithelial cells (Vero, CCL-81,
American Type Culture Collection) were cultured in Dulbeco's modified Eagle's medium (DMEM, Thermo Fisher Scientific). Human rhabdomyosarcoma cells (RD, CCL-136, American Type Culture Collection) were grown in minimal essential medium (MEM, Thermo Fisher Scientific). All cells were maintained in medium supplemented with 10% fetal bovine serum (FBS, Gibco) at 37 °C with 5% CO 2 .
The EV71 BrCr-TR strain was obtained from the Institute of Medical Biology, Chinese Academy of Medical Science. The CVA9 Griggs strain was obtained from the Institute of Biomedical Engineering, Chinese Academy of Medical Sciences, and Peking Union Medical College. The CVB3 Nancy strain was obtained from Wuhan University. All viruses were amplified in Vero cells. Virus titer was measured by the TCID 50 in RD cells using the Reed-Muench formula 37 . Cleavage assay detected by Western blotting assays. HEK293T cells were seeded in 6-well plates and transfected with corresponding plasmids using Lipofectamine ® 2000 Reagent. At 24 hours post transfection, cells were lysed with RIPA lysis buffer (50 mM Tris, pH 7.4, 150 mM NaCl, 1% NP-40, 0.5% sodium deoxycholate, 0.1% SDS) plus protease inhibitor PMSF and subjected to SDS-PAGE. Proteins were separated and transferred to polyvinylidene difluoride (PVDF) membranes. The membranes were then blocked and incubated with respective primary antibodies and horseradish peroxidase (HRP)-conjugated secondary antibodies (Pierce). After washing, membranes were incubated with the Immobilon Western chemiluminescent HRP substrate (Millipore) and subjected to the Bio-Rad Imaging System for imaging analysis.

Antibodies and reagents.
Cleavage assay detected by luciferase assay. HEK293T  Assay of EV71 3C pro inhibition by Rupintrivir using plasmid expression. For Western blotting assays, HEK293T cells were seeded in 6-well plates and transfected with corresponding plasmids. At 7 hours post transfection, cells were treated with 1 μM of Rupintrivir or methanol. At 30 hours post transfection, cells were harvested and subjected to Western blotting as described above.
For luciferase assay, HEK293T cells were seeded in 24-well plates and transfected with corresponding plasmids. At 7 hours post transfection, cells were treated with 1 μM of Rupintrivir or methanol. At 30 hours post transfection, cells were harvested and subjected to luciferase assay as described above.
Construction of i-3CS-GLuc2 stable expression cell line. HEK293T cells were seeded in 6-well plates and transfected with pPB-i-3CS-GLuc2-Flag and a Super PB transposase expression vector. At 30 hours post transfection, selection was performed by adding 4 μg/ml of puromycin in the culture medium. Colonies were further passaged in puromycin-containing medium to get stable cell line. After detection of i-3CS-GLuc2 expression with indirect immunofluorescence and Western Blotting, cell lines were cultured in medium containing 4 μg/ml of puromycin all the time to maintain their stability.
Cleavage assay in HEK293T-i-3CS-GLuc2 cells using Western blotting assays. HEK293T-i-3CS-GLuc2 cells were seeded in 6-well plates and transfected with corresponding plasmids. At 24 hours post transfection, cells were harvested and subjected to Western blot as described above. Z factor determination. 1 × 10 5 HEK293T-i-3CS-GLuc2 cells were seeded in 96-well assay plates (Corning), infected with the EV71 BrCr-TR strain at an MOI of 4, and treated with 100 nM of Rupintrivir or with methanol as negative control. At 24 hours post infection, cells were lysed with 40 μL of passive lysis buffer per well and disrupted by one freeze-thaw between −80 °C and 37 °C. Then 40 μL of coelenterazine (5 μM) were added to the lysates and bioluminescence measurements were made using a Multimode Microplate Reader (Varioskan Flash, Thermo Fisher, Finland). The value of Z factor was calculated using the formula described in a previous report 28 .