The recent outbreak of Zika virus (ZIKV) has imposed a serious threat to public health. Here we report the crystal structure of the ZIKV NS5 protein in complex with S-adenosyl-L-homocysteine, in which the tandem methyltransferase (MTase) and RNA-dependent RNA polymerase (RdRp) domains stack into one of the two alternative conformations of flavivirus NS5 proteins. The activity of this NS5 protein is verified through a de novo RdRp assay on a subgenomic ZIKV RNA template. Importantly, our structural analysis leads to the identification of a potential drug-binding site of ZIKV NS5, which might facilitate the development of novel antivirals for ZIKV.
The outbreak of Zika virus (ZIKV) in the Americas and West Pacific islands in the past year has become a worldwide health concern, affecting more than 60 countries to date1,2. Increasing evidence has linked ZIKV infection to microcephaly in newborn infants3, and to Guillain–Barré syndrome in adults4. The fact that no vaccines or therapeutics for prevention or treatment of ZIKV infection are currently available further deepens the concern. To develop effective antivirals against ZIKV infection, it is urgent to gain a comprehensive structural and mechanistic understanding of the molecular machineries underpinning the life cycle of ZIKV.
ZIKV belongs to the family of flavivirus that includes a variety of mosquito-borne human pathogens, such as dengue virus (DENV1–4), yellow fever virus, West Nile virus, Spondweni virus and Japanese encephalitis virus (JEV)5. The genome of ZIKV is organized into the form of a single positive strand RNA, encoding in total three structural proteins (C, prM/M and E) and seven non-structural (NS) proteins (NS1, NS2A, NS2B, NS3, NS4A, NS4B and NS5)6. Among these, NS5 is the largest NS protein, containing an N-terminal methyltransferase (MTase) domain responsible for viral RNA capping and a C-terminal RNA-dependent RNA polymerase (RdRp) domain for viral RNA synthesis, with evidence indicating that the MTase and RdRp domains cooperate in RNA synthesis initiation and elongation7. In addition, NS5 proteins have been shown to inhibit the type I interferon (IFN) signalling to evade antiviral defence in the host8,9,10,11,12,13,14,15,16. The essential role of NS5 in viral replication and immunosuppression makes it an ideal target for antivirals17. However, the molecular mechanism underlying the enzymatic action of NS5 remains poorly understood. Thus far, crystal structures of full-length NS5 proteins have only been reported for JEV and DENV3 (refs 18, 19). Intriguingly, despite with ∼65% sequence identity (Supplementary Fig. 1), JEV NS5 and DENV3 NS5 adopt different orientations between the MTase and RdRp domains18,19, raising the question of how the MTase and RdRp domains of NS5 cooperate during RNA replication and capping.
To illuminate the structure and mechanism of NS5 proteins, and, more importantly, to explore potential druggable sites for ZIKV, we determined the crystal structure of full-length ZIKV NS5 in complex with S-adenosyl-L-homocysteine (SAH), by-product of cofactor S-adenosyl-L-methionine at 3.3 Å resolution. Our structural analysis reveals that ZIKV NS5 folds into one of the two alternative conformations of flavivirus NS5 proteins, providing functional implication for the conformational dynamics of flavivirus NS5 proteins. We further verify the enzymatic activity of ZIKV NS5 through a de novo RdRp assay using a subgenomic ZIKV RNA as template. Finally, we show that the structure of ZIKV NS5 provides a framework for future development of novel antivirals against ZIKV infection.
Overall structure of ZIKV NS5
We were able to trace nearly the entire sequence of ZIKV NS5 (Fig. 1a), except for the first five N-terminal residues, residues 747–748 in the RdRp domain, and sixteen residues at the C terminus. The structure reveals an N-terminal classic S-adenosyl-L-methionine-dependent MTase domain situated on top of a C-terminal RdRp domain. The MTase domain is dominated by a Rossmann fold, with a seven-stranded β-sheet sandwiched by two α-helices from one side and another α-helix from the other side. Near to the catalytic site, the SAH molecule is surrounded by a set of conserved residues (Supplementary Fig. 2). In addition, the N-terminal extension sequence (α1–α4 in Supplementary Fig. 1) of the MTase domain pairs with its C-terminal extension sequence (α8–β9 in Supplementary Fig. 1) to form a helix bundle and an antiparallel two-stranded β-sheet, adding another structural layer onto the Rossmann fold (Fig. 1b). As with other viral RdRps20, the ZIKV NS5 RdRp adopts a capped right-hand structure with the Palm, Fingers and Thumb subdomains and a priming sequence poised to receive RNA substrates (Fig. 1b). The RdRp domain also harbours two zinc ions, as observed for the NS5 proteins of JEV and DENV3 (refs 18, 19).The associations of the MTase domain with the RdRp domain does not involve extensive interdomain contacts, leading to a modest buried surface area of ∼1,400 Å2. In fact, structural superposition of the MTase domain in full-length NS5 and the recently reported domain alone21 gives a root-mean-square deviation (RMSD) of 0.42 Å over 242 Cα atoms, indicating that the MTase–RdRp association does not lead to considerable conformational change of the MTase domain.
Structural comparison with other flavivirus NS5 proteins
ZIKV NS5 shares ∼68% and ∼66% sequence identity, respectively, with its JEV and DENV3 counterparts (Supplementary Fig. 1). However, these NS5 homologues appear to antagonize the IFN signalling through different mechanisms: JEV NS5 suppresses IFN signalling likely through blocking phosphorylation of the IFN signalling components13, whereas DENV3 NS5 and ZIKV NS5 inhibit the IFN signalling through promoting protein degradation of signal transducer and activator of transcription 2 in an E3 ubiquitin ligase UBR4-dependent or -independent manner10,16. Along the line, we compared the structure of ZIKV NS5 with those of JEV NS5 and DENV3 NS5 (Fig. 2a,b). Remarkably, ZIKV NS5 superimposes well with JEV NS5, with an RMSD of 0.63 Å over 872 Cα atoms (Fig. 2a). In particular, the MTase–RdRp associations of ZIKV NS5 and JEV NS5 are both mediated by the same set of van de Waals contacts, involving the C-terminal extension of the MTase domain (P113, L115, Q117 and W121), and the Index, Ring and Middle fingers of the RdRp domain (Y350, R354, F466 and P584 in ZIKV NS5) (Fig. 2c,d). Subtle structural divergence between ZIKV NS5 and JEV NS5 was mainly observed for the N- and C-terminal extension of the MTase domain, the MTase-RdRp domain linker, and a segment in the Palm subdomain (residues E632-G653 in ZIKV NS5) (Supplementary Fig. 3a). Note that these regions have previously been linked to NS5-mediated immunosuppression13,14. Therefore, such structural divergence may underlie the distinct mechanisms of ZIKV NS5 and JEV NS5 in IFN antagonism. By contrast, structural superposition of ZIKV NS5 and DENV3 NS5 gives a RMSD of 6.06 Å over 844 Cα atoms, attributed in large part to the difference in the relative orientation between the MTase and RdRp domains (Fig. 2b). Unlike the structure of ZIKV NS5 in which the MTase domain sits on the back of the RdRp domain, the MTase domain of DENV3 NS5 approaches towards the front of the RdRp domain, resulting in a more compact conformation (Fig. 2b). Distinct from those of ZIKV NS5 (Fig. 2c,d) and JEV NS5, the MTase–RdRp association of DENV3 is mediated by a set of hydrogen bonding, cation-π and electrostatic interactions between the N- (Q63, E67 and R68) and C-terminal extensions (E252 and D254) of the MTase domain and the Index finger (F348, R352, E356 and K357) of the RdRp domain (Fig. 2e). These interactions of DENV3 NS5 appear to draw the MTase domain towards the NTP entrance of the RdRp domain, resulting in a ∼100° rotation of the MTase domain in relation to the RdRp domain (Fig. 2b). Another prominent structural difference between ZIKV/JEV NS5 and DENV3 NS5 arises from the substrate binding motifs of RdRp, including motif F in the Ring finger and motif G in the Pinky finger22,23 (Fig. 2b). The conformations of these two motifs appear to be stabilized by the MTase–Ring finger association of ZIKV/JEV NS5, but become disordered in DENV3 NS5 due to the loss of the corresponding interactions (Supplementary Fig. 3b).
The fact that the structure of ZIKV NS5 exhibits an extended domain conformation similar to that of JEV NS5, but differently from that of DENV3 NS5, raises a question on the functional implication of these two conformational states of NS5 proteins. On one hand, it is likely that the structures of ZIKV/JEV NS5 diverge from that of DENV3 NS5 through adaptive mutations of specific regions (for example, domain linker) during evolution, as proposed previously24. On the other hand, the high sequence conservation of both domain interfaces (Supplementary Fig. 1) strongly argues that the structures of ZIKV/JEV NS5 and DENV3 NS5 represent two alternative conformations of NS5 that may coexist in solution. Consistently, previous small-angle X-ray scattering analysis suggested the presence of a heterogeneous conformational ensemble of DENV3 NS5 in solution24, and mutations at the two alternative domain interfaces lead to compromised methyltransferase activity or viral replication function of DENV3 NS5 (ref. 19). Additional biochemical and cellular analyses are required to reveal the functional implication of these two alternative conformations of flavivirus NS5 proteins.
De novo RdRp assay of ZIKV NS5
To confirm that the ZIKV NS5 protein used for our structural study represents an active enzyme, we performed a de novo RdRp assay for ZIKV NS5 on a subgenomic ZIKV RNA template (Fig. 3a), using the recombinant ZIKV NS3 helicase domain (NS3-Hel) (Fig. 3b and Supplementary Fig. 4) as a negative control. We observed that the presence of ZIKV NS5 led to a time-dependent increase in the replication of the subgenomic ZIKV RNA at 33 °C (Fig. 3c and Supplementary Fig. 5). However, the reaction product became dominated by a shorter RNA at 23 °C, possibly due to early termination of the replication (Fig. 3c). On the other hand, the presence of ZIKV NS3-Hel failed to yield any RNA product (Fig. 3c). Together, these data not only confirm that the ZIKV NS5 protein used for the structural study is enzymatically active but also provide a basis for further functional characterization of ZIKV NS5.
Identification of potential inhibitor-binding sites
Finally, we asked whether the structure of ZIKV NS5 permits us to identify potential inhibitor-binding sites for its enzymatic inhibition. A previous study, through fragment-based crystallography method, identified a pocket near to the active site of the DENV3 RdRp domain, termed ‘N pocket’, which binds to a small-molecule that inhibits DENV3 NS5-mediated RNA initiation and elongation (Fig. 4a)25. Detailed analysis of this inhibitor-binding site revealed that the critical residues for the inhibitor binding are also conserved in ZIKV NS5, arranged in a similar structural environment (Fig. 4b); therefore, suggesting that the same compound may also be inhibitory to the enzymatic activity of ZIKV NS5. Further enzymatic analysis is needed to test the possibility of applying this DENV3 inhibitor to suppress the activity of ZIKV NS5.
Our structural study of ZIKV NS5 sheds light onto the conformational dynamics and functional regulation of ZIKV NS5. The observation that ZIKV NS5 adopts one of the two defined conformations of flavivirus NS5 proteins provides first evidence on the conservation of domain conformation within NS5 proteins, which may be required for their functional regulation. To confirm the enzymatic activity of the recombinant ZIKV NS5 protein, we developed a de novo RdRp assay of ZIKV NS5 on a subgenomic ZIKV RNA template, which provides basis for future mechanistic characterization of ZIKV NS5. Furthermore, we identified that the small molecular inhibitor-binding site of DENV3 NS5 is structurally conserved in ZIKV NS5, thereby revealing a potential mechanism for functional inhibition of ZIKV NS5. This study provides a foundation for future dissection of the functional coupling between the MTase and RdRp domains and a framework for the design of novel inhibitors against ZIKV infection.
Expression and purification of ZIKV NS5 and NS3 helicase
The DNA sequence encoding full-length ZIKV NS5 or ZIKV NS3-Hel (residues 171–617) was amplified from the cDNA of ZIKV/Macaca mulatta/UGA/MR-766/1947 and inserted into a modified pRSFDuet-1 vector (Novagen) (see Supplementary Table 1 for primer sequences), in which the NS5 or NS3-Hel gene was preceded by an N-terminal His6-SUMO tag and ULP1 (ubiquitin-like protease 1) cleavage site. The obtained plasmids were then transformed into BL21 (DE3) RIL cell strain (Agilent Technologies) for expression. The cells were first grown at 37 °C and then shifted to room temperature when A600 reached 1.0, followed by the addition of 0.4 mM isopropyl β-D-galactoside for induction. After another 18 h of cell growth, the cells were collected and the His6-SUMO-tagged ZIKV NS5 or ZIKV NS3-Hel was purified using a Ni-NTA affinity column. ZIKV NS5 was further purified on a Phenyl Sepharose column (GE Healthcare) for separation from degraded protein products, followed by removal of the His6-SUMO tag through ULP1 cleavage and size-exclusion chromatography on a Superdex 200 16/600 column (GE Healthcare) pre-equilibrated in buffer containing 25 mM Tris, pH 7.5, 500 mM NaCl, 5 mM DTT (dithiothreitol) and 5% glycerol. The ZIKV NS3-Hel fusion protein was first subject to ULP1 cleavage, and subsequently purified on a Phenyl Sepherase column and a Superdex 200 16/600 column pre-equilibrated in buffer containing 25 mM Tris, pH 7.5, 250 mM NaCl, 5 mM DTT and 5% glycerol. SDS–polyacrylamide gel electrophoresis analysis indicated that the purities of NS5 and NS3-Hel proteins were >95% and >90%, respectively. Protein solution of purified NS5 and NS3-Hel, with concentrations of ∼20 and ∼70 mg ml−1, respectively, were stored at −80 °C.
Crystallization and X-ray data collection
Full-length ZIKV NS5 was mixed with SAH and GTP in a 1:3:3 molar ratio for complex formation. Initial crystallization conditions were identified through sparse-matrix screens (Hampton Research Inc.). The crystals were subsequently reproduced by hanging-drop vapour diffusion method at 4 °C, from drops mixed from 1 μl of ZIKV NS5 and 1 μl of precipitant solution (0.7–0.9 M lithium sulfate, 0.1 M MES, pH 6–7). Crystals were soaked for 1 min in a cryoprotectant solution, comprising of crystallization buffer and 20% glycerol, before flash frozen in liquid nitrogen.
The X-ray diffraction data for ZIKV NS5 were collected on the BL 5.0.3 beamline at the Advanced Light Source, Lawrence Berkeley National Laboratory. The diffraction data were indexed, integrated and scaled using the HKL2000 program26. The structure was solved using the molecular replacement method in PHASER27, with the structure of Japanese encephalitis virus NS5 (PDB ID: 4K6M) as search model. The resulting electron density revealed that there are two molecules of ZIKV NS5 in each asymmetric unit. Despite being present in the crystallization mixture, GTP molecules were not modelled, presumably due to low occupancy under the crystallization condition. The structure of ZIKV NS5 was improved by iterative model building and refinement with Coot28 and PHENIX29 software packages. The same R-free test set was used throughout the refinement. The statistics for data collection and structural refinement of ZIKV NS5 is summarized in Table 1.
De novo RdRp assay
For ZIKV, the de novo RdRp reaction (20 μl) contained 50 mM Tris (pH 8.0), 10 mM NaCl, 5 mM MgCl2, 2 mM MnCl2, 10 mM DTT, 0.5 mM ATP, 0.5 mM UTP, 0.5 mM GTP, 5 μM CTP, 15 μCi of [α-32P] (10 μCi μl−1, 3,000 Ci mmol−1; Perkin-Elmer), 1 μg of RNA template and 2 μg of ZIKV NS5 protein or ZIKV NS3-Hel. The RNA template was in vitro transcribed from a PCR product using T7 polymerase (New England BioLabs). The PCR product contained a T7 promoter, followed by a cDNA fragment representing a ZIKV subgenome with deletion of nucleotides 171–10,343 (GenBank accession no. KU963573.2). The de novo RdRp reaction mixtures were incubated at 23 °C for 30 min, or 33 °C for 30, 60 and 120 min. The final reactions were further extracted with phenol–chloroform and precipitated with isopropanol. The RNA pellet was dissolved in 20 μl of 1 × denaturing gel loading dye, and loaded onto a 10% denaturing polyacrylamide gel with 7 M urea. 32P-labelled RNA results were detected via the autoradiograph of the PAGE gel.
Coordinates and structure factors for ZIKV NS5–SAH complexes have been deposited in the Protein Data Bank under accession code 5TMH. The PDB accession codes 5TMH, 5JJR, 4K6M and 4V0Q and GenBank entry KU963573.2 were used in this study. All other data are available from the corresponding authors on reasonable request.
How to cite this article: Wang, B. et al. The structure of Zika virus NS5 reveals a conserved domain conformation. Nat. Commun. 8, 14763 doi: 10.1038/ncomms14763 (2017).
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This work was supported by March of Dimes Foundation (1-FY15-345), Kimmel Scholar Award from Sidney Kimmel Foundation for Cancer Research and NIH (1R35GM119721) (to J.S.). The Berkeley Center for Structural Biology is supported, in part, by the National Institutes of Health, National Institute of General Medical Sciences and the Howard Hughes Medical Institute. The Advanced Light Source is supported by the Director, Office of Science, Office of Basic Energy Sciences and of the US Department of Energy under Contract No DE-AC02-05CH11231.
The authors declare no competing financial interests.
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Wang, B., Tan, XF., Thurmond, S. et al. The structure of Zika virus NS5 reveals a conserved domain conformation. Nat Commun 8, 14763 (2017). https://doi.org/10.1038/ncomms14763
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