Tylophorine analogs have been shown to exhibit diverse activities against cancer, inflammation, arthritis, and lupus in vivo. In this study, we demonstrated that two tylophorine analogs, DCB-3503 and rac-cryptopleurine, exhibit potent inhibitory activity against hepatitis C virus (HCV) replication in genotype 1b Con 1 isolate. The inhibition of HCV replication is at least partially mediated through cellular heat shock cognate protein 70 (Hsc70). Hsc70 associates with the HCV replication complex by primarily binding to the poly U/UC motifs in HCV RNA. The interaction of DCB-3503 and rac-cryptopleurine with Hsc70 promotes the ATP hydrolysis activity of Hsc70 in the presence of the 3′ poly U/UC motif of HCV RNA. Regulating the ATPase activity of Hsc70 may be one of the mechanisms by which tylophorine analogs inhibit HCV replication. This study demonstrates the novel anti-HCV activity of tylophorine analogs. Our results also highlight the importance of Hsc70 in HCV replication.
Tylophorine analogs are a class of natural products first isolated from the plant Tylophora Indica 1. Tylophora Indica and Tylophora Ovata were traditionally used for the treatment of asthma in India2 and arthritis in China3. This group of analogs has also shown broad activities against cancer4, 5, inflammation5, 6, arthritis3, and lupus7 in vivo. Tylophorine analogs have been shown to reduce the rate of elongation of polypeptide chain to inhibit global protein synthesis8, which has a more profound effect on cellular regulatory proteins with short half-lives8. No other known anticancer drug or protein synthesis inhibitors exhibits the same novel activity. Only vascular endothelial growth factor receptor 2 (VEGFR2) has been identified for the antiangiogenic activity of tylophorine9. In addition, we recently identified that tylophorine analog DCB-3503 regulated translation of cyclin D1 through allosteric regulation of heat shock cognate protein 70 (Hsc70)10.
Hepatitis C virus (HCV) infects approximately 3% of the world’s population and is one of the top reasons for the development of liver cirrhosis and hepatocellular carcinoma11. The nonstructural (NS) proteins are responsible for replication of HCV RNA and virus particle assembly and are primary antiviral targets12, 13. The initial standard of care for HCV infection is peginterferon alpha combined with ribavirin for 48 weeks for HCV genotype 1, or 24 weeks for HCV genotypes 2 or 3. Peginterferon treatment showed a sustained viral response (SVR) rate of less than 50% HCV genotype 1 infection, the most prevalent strain in Europe and North America11. The recently developed direct-acting antivirals (DAAs) targeting against NS proteins significantly improved SVRs to as high as 99% and broadened the spectrum of patients to all genotypes as well as HCV with cirrhosis patients14,15,16. However, the high cost of current treatment restricts broad patient access, especially to the DAAs. In addition, targeting host factors by small molecules could illustrate the important functions of host factors involved in viral replication and pathogenesis17.
Tylophorine analogs inhibit selected set of protein syntheses by inhibiting the elongation step8. Both HCV replication and protein synthesis take place on the endoplasmic reticulum (ER). Therefore, we explored whether tylophorine analogs could inhibit replication of HCV. We hypothesized that DCB-3503 inhibits elongation by interacting with host factors; thus we aimed to identify cellular target(s) of the tylophorine analogs regulating translation and viral replication. Using biotinylated-DCB-35034 and -rac-cryptopleurine18, we identified heat shock cognate protein 70 (Hsc70) as one of the cellular targets of tylophorine analogs. Hsc70 is a constitutively expressed heat shock protein family member with an ATPase N-terminal nucleotide-binding domain (NBD) and a C-terminal substrate-binding domain (SBD)19. The ATPase activity of Hsc70 could be regulated by small-molecule inhibitors and/or cochaperone proteins20.
In this study, we demonstrated that DCB-3503 and rac-cryptopleurine potently inhibit HCV replication. They both exhibit anti-HCV activity by promoting the ATP hydrolysis activity of Hsc70 through binding to the 3′ poly U/UC motif of HCV RNA. This allosteric regulation of Hsc70 function alters the interaction between Hsc70 and its associated HCV protein and RNA, and also perturbs the homeostasis of the HCV replication complex, thus inhibiting translation of HCV RNA.
Tylophorine analogs exhibit anti-HCV activity in HCV genotype 1b replicon cells
We previously demonstrated that DCB-3503 and its analogs inhibit protein synthesis8, 21. Protein synthesis is one of the most critical steps in HCV replication11; therefore, we examined the anti-HCV activity of the tylophorine analogs, DCB-3503 and rac-cryptopleurine8, 21,22,23 in Huh-luc/neo-ET cells harboring the HCV genotype 1b Con 1 isolate. Treatment with DCB-3503 and rac-cryptopleurine decreased HCV RNA levels (Fig. 1a and b) and the expression of NS3 and NS5A proteins in a dose-dependent manner (Fig. 1c and d). No resistant clones could be isolated after selection with a 10-fold EC50 concentration of DCB-3503 (300 nM) and rac-cryptopleurine (30 nM) for three weeks (Figure S1a). While resistant clones emerged under the selection of a 10-fold EC50 concentration of meso-tetrakis-porphyrin compound 6 (200 nM), a potent HCV inhibitor developed in our laboratory that targeta viral protease (Figure S1a)24.
Tylophorine analog specifically interacts with Hsc70
Since we could not isolate resistant clones to DCB-3503 or rac-cryptopleurine, we hypothesized that tylophorine analogs may inhibit viral replication by affecting host factors. Biotinylated DCB-3503 and rac-cryptopleurine were synthesized to determine the molecular target(s) of the tylophorine analogs. The tethered biotin group was connected to the 3-position on the tylophorine backbone as directed by our structure–activity relationship study8, 10, 21,22,23 (Figure S1b). The anti-HCV activity and cytotoxicity of both parental compounds and biotinylated derivatives are shown in Table S3. The flow chart of affinity purification was shown in Figure S1c. The proteins bound to biotinylated-DCB-3503 and -rac-cryptopleurine were separated by SDS-PAGE and visualized by silver staining. Proteins that specifically eluted by rac-cryptopleurine were identified by LTQ Orbitrap mass spectrometry10. Western blot analysis results revealed that biotinylated DCB-3503 and rac-cryptopleurine bound to Hsc70 when Huh-luc/neo-ET cell lysate or recombinant polyhistidine (His)-tagged Hsc70 was run through the compound matrix column (Fig. 2a). Hsp70 or Hsp90 did not bind to the affinity matrix under the same conditions (Fig. 2a). Increasing concentration of ATP (Fig. 2b) but not UTP (Fig. 2c) eluted the compound-bound Hsc70. The binding was also dependent on ionic strength: 0.4 M NaCl eluted the bound Hsc70 from the affinity matrix (Figure S1d). Western blot results showed that both DCB-3503 and rac-cryptopleurine bound to the NBD of recombinant Hsc70 (residue 1–385) (Fig. 2d). The binding affinity of DCB-3503 and rac-cryptopleurine to Hsc70 did not change when a D206S mutation was introduced into the ATPase pocket in the NBD of Hsc70 (Fig. 2e)25. In order to determine antibody specificity, we expressed and purified recombinant Hsp70. Western blot results indicated that the Hsc70 antibody we used recognized only recombinant Hsc70 but not Hsp70 (Figure S1e). Isothermal titration calorimetry (ITC) revealed that DCB-3503 and rac-cryptopleurine showed similar binding affinities to the full length (FL) and the NBD of Hsc70 (Table 1 and Figure S1f ). The protein level of Hsc70 remained unchanged throughout the treatment with DCB-3503 or rac-cryptopleurine for up to 72 hours (Figure S1g).
Hsc70 is involved in the anti-HCV activity of DCB-3503
We constructed an Hsc70 overexpression plasmid with silent mutation on the shRNA targeting sites (rHsc70-1, and rHsc70-2, Fig. 3a) to determine the off-target effect of shRNA. Down-regulation of Hsc70 with shRNA reduced HCV RNA replication and suppressed expression of NS3 and NS5A (lanes 3 and 5 in Fig. 3b). The RNAi phenotype was partially rescued by over-expressing HA-rHsc70s (Fig. 3b), suggesting that suppression of Hsc70 was responsible for the down-regulation of HCV replication. Transfection of wild type (WT) HA-tagged Hsc70 also inhibited HCV RNA replication (Fig. 3b, quantitative results of protein expression are shown in Figure S2a). shRNA knockdown of Hsc70 for 48 hours enhanced the anti-HCV activity of DCB-3503 as reflected by the resultant decrease in HCV RNA, NS3, and NS5A levels (Fig. 3c, quantitative results of protein expression were shown in Figure S2b). Reduced expression of Hsc70 by shRNAs did not significantly affect cell growth (Figure S2c). Complete knockout of Hsc70 with combination of two shRNAs is lethal to cells; thus, a more significant anti-HCV effect could not be demonstrated. Overexpression of either WT or D206S mutant HA-tagged Hsc70 inhibited expression levels of HCV RNA and NS proteins, and further enhanced the anti-HCV effect of DCB-3503 (Fig. 3d, quantitative results of protein expression are shown in Figure S2d) without changing the cell growth curve (Figure S2e). Treatment with DCB-3503 inhibited translation of HCV in vitro (Figure S2f), and pretreatment of HLN-cured cells with 30 nM DCB-3503 for 24 hours reduced the cells’ ability to support HCV replication by about 2-fold (Figure S2g). Furthermore, the replication rate of HCV RNA transfected into HLN-cured cells with reduced Hsc70 expression by shRNA was about 3-fold slower than those HLC-cured cells without Hsc70 shRNA treatment (Fig. 3e). The Hsc70 expression levels are shown in Figure S2h. Alteration of expression of Hsc70 is related to HCV RNA replication.
Hsc70 is associated with the HCV replication complex
Hsc70 exhibits its function via association with different cellular complexes26. We thus examined whether Hsc70 is associated with the HCV replication complex. Post-nuclear supernatant of untreated, DCB-3503-treated or rac-cryptopleurine-treated Huh-luc/neo-ET cells were fractionated on continuous optiprep iodixanol density gradients (Figs 4a–c, S2i). The optiprep density gradients separated membrane vesicles (Alix and Hrs as markers in fractions 1–6, and GRP 78 as marker in fractions 1–2), and endoplasmic reticulum (ER) (GRP78 and Calenxin as markers in fractions 7–11) (Fig. 4a). In untreated control cells, HCV RNA, NS3, and NS5A exhibited the same sedimentation with the membrane vesicles and ER in fractions 5–11 (Fig. 4a and b), a result consistent with the density reported earlier27. In cells treated with DCB-3503 or rac-cryptopleurine; however, HCV RNA, NS3, and NS5A agglomerated with the ER in fractions 8–11 (Fig. 4a and b). Hsc70 showed the same sedimentation shift with the membrane vesicles (fractions 1–3) and ER (fractions 7–11) in both untreated control and drug-treated cells (Fig. 4a). DCB-3503 accumulated in the first two fractions with 60–80 nM concentration where Hsc70 was primarily located (Fig. 4c). In addition, DCB-3503 was found in fractions 3–12 at around 1 nM concentration (Fig. 4c). The amount of rac-cryptopleurine in the fractions was too low to detect with LC/MS/MS. The cosedimentation of Hsc70 with HCV NS3, NS5A, and ER marker Calnexin was disrupted when the cytoplasmic fraction was treated with 0.5 M NaCl or RNase A before centrifugation to isolate crude HCV replicon (Fig. 4d). All the examined proteins were found only in the supernatant fraction with addition of 0.1% SDS (Fig. 4d). NS3 and NS5A remained in the membrane-rich pellet fraction when ionic strength was changed with NaCl, or when the RNA was depleted with RNase treatment (Fig. 4d). However, addition of 0.5 M NaCl or 0.1 μg/μl of RNase released Hsc70 from the membrane-rich pellet fraction to the supernatant (Fig. 4d). Addition of 0.1% SDS totally disrupted the membrane structure and released NS3, NS5A, and Hsc70 to the supernatant (Fig. 4d).
Treatment with DCB-3503 promotes binding of Hsc70 to HCV RNA
Given the result of the co-sedimentation of Hsc70 with HCV NS proteins and RNA, we further examined the association of Hsc70 with HCV replication complex. Real-time PCR results showed that more than 30% of HCV RNA was present in the Hsc70 immunoprecipitated complex (Fig. 5a). The level of HCV RNA in the input and Hsc70-associated complex did not change significantly after treatment with up to100 nM DCB-3503 for 6 hours. However, the amount of Hsc70-associated NS5A and NS5B were reduced with treatment of 30 nM and 100 nM of DCB-3503 for 6 hours (Fig. 5a). NS3/4 A, NS4B, or host RNAs (β-actin and survivin) did not bind to Hsc70 under the same conditions (Figs 5a and S3a,b). RNase A treatment decreased the amount of NS5A and NS5B associated with Hsc70 (Figure S3c). We then analyzed the association between NS5B and Hsc70 and between HCV RNA and NS5B using a co-immunoprecipitation method. DCB-3503 treatment reduced the amount of Hsc70 bound to HA-tagged NS5B when immunoprecipitated with HA antibody (Figure S3d). The association of NS5B and Hsc70 to biotinylated HCV RNA was also decreased with addition of DCB-3503 (Figure S3e). Hsc70 can bind to the AU-rich elements in the 3′ untranslated region of Bim mRNA28. Thus, we generated constructs with different specific motifs of the 3′ nontranslated region (3′ NTR) of HCV genotype 1b RNA to determine the Hsc70 binding RNA sequence (Fig. 5b)29. Hsc70 bound to all the biotinylated RNA fragments containing AUUUA and poly U/UC sequences (Fig. 5c). Biotinylated RNA containing only the AUUUA sequence showed relatively weak association with Hsc70 compared with poly U/UC RNA (Fig. 5d). Hsc70 was not associated with Poly A RNA under the same conditions (Fig. 5c). The association of short poly U/UC RNA with Hsc70 was comparable to that of other longer RNA fragments (Fig. 5c), which suggests that the poly U/UC sequence is essential but not necessarily sufficient for binding to Hsc70. The poly U/UC RNA below refers to the short form of HCV genotype 1b. Poly U/UC RNA did not bind to fragments of Hsc70 (Figure S3f) or Hsp70 (Figure S3g) under the same conditions. Addition of increasing concentrations of unlabeled poly U/UC or AU + UC RNA competed with the association of biotinylated poly U/UC RNA to Hsc70 in a dose dependent manner (Fig. 5d). As much as 9-fold of unlabeled AUUUA RNA could not compete with poly U/UC binding with the same efficiency (last three lanes, Fig. 5d). Deletion of the poly U/UC region in the 3′ NTR could not support HCV replication (Figure S3h). Since the poly U/UC region in the 3′NTR of the HCV genome is conserved through all genotypes29, we then generated the poly U/UC region of HCV genotype 2a JFH1 clone (Fig. 5e) and performed the RNA-binding assay under the same conditions. Biotin labeled poly U/UC RNA of HCV genotype 2a also bound to Hsc70 and the increasing amount of unlabeled poly U/UC RNA decreased the association to Hsc70 (Fig. 5e) as poly U/UC RNA from HCV genotype 1b (Fig. 5d).
Tylophorine analogs stimulate the ATPase activity of Hsc70 in the presence of poly U/UC RNA
The association between Hsc70 and interacting proteins or RNAs is primarily regulated by its ATPase activity19. We determined the ability of tylophorine analogs to regulate the ATPase activity of Hsc70. DCB-3503 and rac-crytopleurine stimulated ATP hydrolysis of FL Hsc70 only at relatively high concentrations (Figure S4a and b). Meanwhile, the K m of Hsc70 for ATP-binding was reduced to about 50% by DCB-3503 or rac-cryptopleurine in the presence or absence of poly U/UC RNA (Fig. 5f and g). Addition of an equal amount of poly C RNA into the reaction did not change the K m for ATP-binding by DCB-3503 and rac-cryptopleurine under the same conditions (Fig. 5f and g). Hsp70 inhibitor 2-phenylethanesulfonamide (PES)25 did not change K m (Fig. 5h), while PES inhibited hydrolysis of ATP by increasing K m for ATP-binding in the presence of poly U/UC RNA (Fig. 5h). The V max of Hsc70 for ATP hydrolysis did not change significantly under the same conditions by DCB-3503, or rac-cryptopleurine, or PES (Figure S4c–e).
Co-chaperone protein BAG1 is involved in the anti-HCV activity of tylophorine analogs
Co-chaperone proteins regulate the ATPase activity of Hsc70 by modulating the ATP/ADP hydrolysis cycle30. The co-chaperone protein BAG-1 is bound to a conserved BAG domain of Hsc70 that interacts with its ATPase domain30. To determine the function of BAG1 in the anti-HCV activity of the tylophorine analogs, we constructed an HA-tagged BAG1 plasmid and transfected it into Huh-luc/neo-ET cells. The expression level of BAG1 was not affected by DCB-3503 treatment for up to 6 hours (Fig. 6a); however, the amount of BAG1 that bound to Hsc70 was decreased with the DCB-3503 treatment (Fig. 6a). Transfection of HA-tagged BAG1 enhanced the inhibitory activity of DCB-3503 and rac-cryptopleurine on HCV RNA replication, as well as expression levels of NS3 and NS5A (Fig. 6b,c). The expression level of HA-BAG1 was decreased with DCB-3503 and rac-cryptopleurine treatment for 48 hours (Fig. 6b,c).
The tylophorine analogs have exhibited various activities, yet the only molecular target VEGFR2 revealed for this group of compounds was associated with their anti-cancer activities9. One report has suggested that tylophorine or (–)-(R)-tylophorine attenuated HCV IRES-mediated translation by suppressing expression of cyclin A231. However, results of our structure–activity relationship studies suggested that tylophorine was not a functional analog of DCB-3503 and rac-cryptopleurine8, 21,22,23. Our study revealed that DCB-3503 stimulated the ATPase activity of Hsc70, thus inhibited translation of cyclin D1 mRNA10. In this study, we evaluated both five- and six-membered E-ring tylophorine analogs as potent inhibitors of HCV replication (Figures 1 and S1a). No resistant clones could be isolated with either DCB-3503 or rac-cryptopleurine treatment (Figure S1a), suggesting that the tylophorine analogs inhibit HCV replication through modulation of the functions of the host’s factor(s).
Hsc70 is associated with the HCV replication complex
Host chaperones and co-chaperones play important functions in the assembly of the viral replication complex and the replication of the viral genome. Hsc70 participated in the RNA-dependent replication of sindbis virus32, influenza virus33, rotavirus34, and dengue virus35. Hsc70 also associated with lipid droplet in HCV-infected cells36. Suppression of Hsc70 expression using shRNAs decreased the infectivity of the HCV J6/JFH virion36. DNAJC14 regulated the chaperone activity of Hsp70; over-expression of DNAJC14 disrupted the stoichiometry of the chaperone/substrate and assembly of the yellow fever virus replication complex37.
We demonstrated that HCV RNA mediated the binding of Hsc70 to the HCV replication complex (Figs 4 and 5). Part of Hsc70 exhibited the same sedimentation with NS3, NS5A, and HCV RNA in the continuous gradient fractions (Fig. 4a,b). The association of Hsc70 to the membrane-rich fraction containing the HCV replication complex was disrupted by changing the ionic strength or RNase treatment, which suggested that the association was dependent on RNA (Fig. 4d and S3c). DCB-3503 treatment perturbed the association of NS5A and NS5B to Hsc70 (Figures 5a and S3d,e), but increased the amount of HCV RNA bound to Hsc70 (Fig. 5a). Hsc70 specifically bound to the poly U/UC RNA motif in both HCV genotypes 1b and 2a (Figs 5b–e and S3f,g). The poly U/UC RNA motif is critical for the efficient translation and replication of HCV RNA efficiently38, 39. Deletion of the poly U/UC sequence inhibited replication of HCV in subgenomic replicon cells (Figure S3f)29, 38. An HCV viral genome lacking this element was not infectious40. Therefore, we presume that DCB-3503 and rac-cryptopleurine could also inhibit replication of other genotypes, for example HCV genotype 2a and its quasispecies that maintain the 3′NTR poly U/UC motif. Poly U/UC was essential for binding to replication factors like the FUSE binding protein41 and hnRNP A142. These RNA-binding proteins regulated translation through either stabilization of RNA or promotion of RNA decay43. A single nucleotide base change sharply reduced the binding affinity between Hsc70 and its associated AUUUA motif in the 3′ untranslated region of host mRNAs10. We found that tylophorine analogs did not inhibit replication of HIV or HBV (results not shown). HIV and HBV have very different sequences from that of HCV, especially in that they do not contain the poly U/UC motif in the 3′NTR. These results suggest that Hsc70 is associated with HCV replication complex preferentially through binding to the uridine rich motif in the 3′NTR.
Two previous reports demonstrated that suppression of Hsc70 by using siRNAs or small molecule inhibitors did not affect HCV RNA replication but rather impacted on the release of virons36, 44. The conflict results may be due to the genotype difference of the Con1 isolate used in the present study from that of the J6/JFH isolated with infectivity36, 44. In addition, sequence and structure differences in the regulatory elements of HCV, like 5′NTR and 3′NTR may require different regulating elements that contribute to differential infectivity and replication45. Therefore, it is reasonable that we obtained results there were different from the previous reports36, 44.
Hsc70 is involved in HCV replication through regulating the translation of HCV RNA
We identified Hsc70 as one of the molecular targets of functional tylophorine analogs using biotinylated-DCB-3503 and -rac-crytopleurine (Figures 2 and S1). The function of Hsc70 is regulated by communications between NBD and SBD. The ATP-bound form of Hsc70 has a “loose” configuration with low affinity for substrates; the ADP-bound state of Hsc70 shows high affinity with associated proteins or RNA46, and favors degradation of substrates47. For example, binding of Hsc70 but not Hsp70 to CHIP promoted its degradation through ubiquitination48. ATP hydrolysis of Hsc70 NBD induces a conformational switch in the adjacent SBD that enhances its binding affinity to substrates.
The binding between Hsc70 and tylophorine was affected by ATP concentration (Fig. 2b,c). DCB-3503 and rac-cryptopleurine bind to the D206S ATPase mutant form of Hsc70, suggesting that the functional ATPase pocket was not required for the interaction (Fig. 2e). Either attenuation of Hsc70 expression level or ectopic expression of the WT or D206S mutant form of Hsc70 enhanced the anti-HCV activity of DCB-3503 (Figs 3b–d and S2a,b, and d). The binding of DCB-3503 or rac-crytopleurine to Hsc70 stimulated its ATPase activity in the presence of the poly U/UC motif of HCV RNA (Fig. 5f,g) without affecting Hsc70 protein expression (Figure S1g). Over-expression of co-chaperone protein BAG-1, which regulates the chaperone activity of Hsc70 by promoting ATP hydrolysis function of Hsc7049, significantly enhanced the anti-HCV activities of DCB-3503 and rac-cryptopleurine (Fig. 6b,c). Therefore, modulating the homeostasis of the ATP/ADP hydrolysis cycle of Hsc70 by tylophorine analogs is related to the inhibitory activity to HCV RNA replication. The HCV RNA associated to Hsc70 in the ADP binding state may be sent to degradation as other substrates of Hsc70. Suppression of Hsp70 expression by its inhibitor, quercetin, attenuated the IRES-mediated translation of HCV J6/JFH virus50. It is also possible that perturbation of Hsc70 function markedly reduced the activities of NS5A and NS5B in the reduced level of free HCV RNA. The around 1 nM concentration of DCB-3503 accumulated in each fraction of fractions 5–12 (Fig. 4c) revealed that DCB-3503 could be associated with protein or a subcellular complex instead of existing in the free form. The concentration should be decreased sharply from fraction 3–12 if DCB-3503 was in the free form. Only co-localization of DCB-3503, NS proteins, and Hsc70 could make this possible. Regulating the ATPase activity of Hsc70 by DCB-3503 and rac-cryptopleurine may be one of the mechanisms by which these compounds modulate HCV replication.
Allosteric regulation of Hsc70 is an alternative strategy to regulate HCV replication
ATPase activity of Hsc70 could be regulated by co-chaperones and/or small molecules, including the Bag (Bcl 2-associated athanogene) family of proteins30, 49, the Hsp40 family proteins51, the immunosuppressive agent 15-deoxyspergualin (DSG)52, or lycoricidine and analogs53, 54. DSG is associated with the EEVD domain in the C-terminal of Hsc70 and Hsp9055. N-substituted benzyl matrinic acid derivatives, ( + )-lycoricidine and analogs inhibited HCV replication through suppression of Hsc70 expression53, 54, 56.
Hsc70 is an abundant cellular protein; therefore, ectopic expression of Hsc70 could not suppress HCV replication (Fig. 3b–d)57. Constitutive deletion of Hsc70 is embryonically lethal in mice, causing defects in multiple organs58. We also observed that knockdown of Hsc70 by combined shRNAs induced cell death. Thus, allosterically modulating ATPase activity of Hsc70 could be a better option to perturb its function rather than decreasing its expression. DCB-3503 and rac-cryptopleurine binds to the NBD of Hsc70 but not HSP90 nor Hsp70 (Figures 2 and S1d) without changing the expression of Hsc70 (Figure S1g). Ectopic expression of BAG1, which promoted ATP hydrolysis activity of Hsc7030, significantly enhanced the anti-HCV activity of tylophorine analogs (Fig. 6). The allosteric regulation of Hsc70 by DCB-3503 and rac-cryptopleurine is distinct from that of existing Hsc70 inhibitors and has not been reported previously. To our knowledge, the tylophorine analogs are the first known class of small molecules that associated with the NBD of Hsc70 and promote the hydrolysis of ATP (Fig. 5f and g).
Taken together, we propose the following model for the mechanisms of action for the anti-HCV activity of functional tylophorine analogs. DCB-3503 or rac-cryptopleurine binds to the NBD of Hsc70 independent of the intact ATP pocket. The binding stimulates the ATP hydrolysis of Hsc70 in the presence of the poly U/UC motif of HCV RNA, and thus inhibits translation. The tylophorine analogs may be potentially used with other anti-HCV agents to attenuate HCV replication. We demonstrated that DCB-3503 exhibited anti-cancer and anti-arthritis activities4, 5, 10; therefore, this group of tylophorine analogs could have special advantages for the treatment of cancer and/or autoimmune diseases patients infected with HCV. However, many questions remain to be investigated. For example, the exact tylophorine binding site(s) of Hsc70 is (are) still unclear due to our failed attempt to determine the Hsc70-DCB-3503 or Hsc70-rac-cryptopleurine complex by crystallography. Will the specific binding to the poly U/UC motif in HCV genotype 2a also be related to anti-HCV activity? And, the dynamic regulation by the tylophorine analogs of ATP/ADP turnover in Hsc70 remains unexplained.
Materials and reagents
Cell culture media and fetal bovine serum (FBS) were purchased from Invitrogen. All reagents were purchased from Sigma-Aldrich (St. Louis, MO) except for those otherwise noted. The DCB series of compounds were synthesized in Dr. Baker’s laboratory. rac-Cryptopleurine and biotinylated-rac-cryptopleurine were synthesized in Dr. Alois Fürstner’s laboratory. The YXM series of compounds were synthesized in Dr. Kuo-Hsiung Lee’s laboratory. The PA series of compounds were provided by Dr. Shishan Yu22. 2-Phenylethanesulfonamide (PES) was purchased from Sigma–Aldrich. Information for plasmid construction and real-time PCR primers are provided in Tables S1 and S2, respectively.
The affinity purification method was adopted from a method reported by Emami et al.59. Cells were lysed in protein-binding buffer [PBB, 20Mm Hepes, pH 7.9, 100 mM NaCl, 0.5 mM EDTA, 0.5% Nonidet P-40, 6 mM MgCl2, 5 mM 2-mercaptoethanol, complete protease inhibitor (Roche)]. Biotinylated-rac-cryptopleurine and -DCB-3503 were bound overnight at room temperature to a 50% slurry of streptavidin–agarose beads (Invitrogen) in buffer containing 50% DMSO and 50% PBB. Beads were washed to remove unbound compound and then incubated with pre-cleared whole-cell lysates or recombinant protein in 2.5% BSA. Bound proteins were eluted, either specifically with rac-cryptopleurine or DCB-3503, or with a buffer specified in the figures. Proteins that remained bound to beads were eluted with SDS loading buffer. Samples were separated with SDS PAGE, and examined by Western blot or silver staining. Specific bands from silver-stained gel were analyzed by LTQ Orbitrap mass spectrophotometry (Yale University W.M. Keck Foundation Biotechnology Resource Laboratory).
Data were analyzed by a two-tailed student’s t-test (Microsoft Office Excel). The difference was considered to be statistically significant when p < 0.05.
All data generated or analyzed during this study are included in this published article and its Supplementary Information files.
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We are indebted to Dr. Ralf Bartenschlager for the Huh-luc/neo-ET and Huh 9-13 replicon cell lines, and pFK I389 Lucubineo NS3-3′ plasmid. We thank Dr. Michael Gale Jr. for the pcDNA3.1 HCV NS3/4 A, pcDNA 3.1 HCV NS5A plasmids. We thank Dr. Baker and Yuri Ahuja for proofreading the manuscript. We thank Kathy Stone and Tom Abbott from the Yale Cancer Center Mass Spectrometry Resource and W.M. Keck Foundation Biotechnology Resource Laboratory for LTQ Orbitrap mass spectrometry analysis. We thank Ewa Folta-Stogniew at the Biophysics Resource of W.M. Keck Foundation Biotechnology Resource Laboratory for assistance with the ITC experiment. Dr. Yung-Chi Cheng is a fellow of the National Foundation for Cancer Research. This work was supported by grants CA177584-01 from National Institute of Health to KHL, PO1 CA154295 from National Cancer Institute, 5RO1 AI 038204 from National Institute of Health, and a gift from William H Prusoff Foundation to YCC, Macao Science and Technology Development Fund 041/2014/A1, Research Fund of the University of Macao MYRG2014-00161-ICMS-QRCM, MYRG2014-00153-ICMS-QRCM, and MYRG2016-00105-ICMS-QRCM to YW. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
The authors declare that they have no competing interests.
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Wang, Y., Lee, S., Ha, Y. et al. Tylophorine Analogs Allosterically Regulates Heat Shock Cognate Protein 70 And Inhibits Hepatitis C Virus Replication. Sci Rep 7, 10037 (2017). https://doi.org/10.1038/s41598-017-08815-z
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