The recent outbreak of Zika virus (ZIKV) has infected over 1 million people in over 30 countries. ZIKV replicates its RNA genome using virally encoded replication proteins. Nonstructural protein 5 (NS5) contains a methyltransferase for RNA capping and a polymerase for viral RNA synthesis. Here we report the crystal structures of full-length NS5 and its polymerase domain at 3.0 Å resolution. The NS5 structure has striking similarities to the NS5 protein of the related Japanese encephalitis virus. The methyltransferase contains in-line pockets for substrate binding and the active site. Key residues in the polymerase are located in similar positions to those of the initiation complex for the hepatitis C virus polymerase. The polymerase conformation is affected by the methyltransferase, which enables a more efficiently elongation of RNA synthesis in vitro. Overall, our results will contribute to future studies on ZIKV infection and the development of inhibitors of ZIKV replication.
Zika virus infection has caused human birth defects and Guillain-Barré Syndrome1,2. ZIKV belongs in the genus Flavivirus of the Flaviviridae family, which also includes the important human pathogens Japanese encephalitis virus (JEV) and the Dengues virus (DENV)3. The flavivirus genome is a positive-sense RNA of 11-kb in length that contains a 5′ cap structure but lacks a polyA tail. The RNA encodes a long open reading frame that is translated into a polyprotein that is subsequently processed by viral and host proteases into three structural and seven nonstructural proteins3.
Nonstructural protein 5 (NS5) is essential for the replication of the flaviviral RNA genome4,5,6. The N-terminal portion of NS5 contains a methyltransferase (MT), followed by a short linker that connects to the RNA-dependent RNA polymerase (RdRp). The MT adds the 5′ RNA cap structure to facilitate translation of the polyprotein and to decrease elicitation of the host innate immune response7,8,9. The RdRp initiates RNA synthesis by a de novo mechanism wherein a single-nucleotide triphosphate serves as a primer for nucleotide polymerization10,11,12. Herein we report the crystal structure of the Zika virus NS5 protein and the structure of the RdRp domain. The MT was found to affect the conformation of the RdRp domain and increase RNA synthesis.
Crystal structure of the ZIKV NS5
We expressed the full-length NS5 from ZIKV strain MR766 that was originally isolated from Uganda Africa and determined its crystal structure at 3.0 Å resolution (Table 1, Supplementary Fig. 1). The polypeptide chains are well defined except for the N-terminal four residues and the C-terminal 16 residues (Fig. 1a, Supplementary Fig. 2). The MT is complexed with S-adenosyl-L-homocysteine (SAH), and the RdRp adopts a classic ‘right-hand’ structure consisting of three subdomains: fingers, palm and thumb (Fig. 1a,b). Two zinc ions are found in the fingers subdomain and at the junction of the palm and thumb subdomains of the RdRp.
The overall structure of the ZIKV NS5 has striking similarities to that of the JEV NS5, with the RMS deviation of 0.55 Å for 751 Cα atoms (Fig. 2a). The MT of both proteins are also located at an acute angle to the RdRps. The ZIKV MT is in a distinct orientation relative to the DENV MT. Due to a short 310-helix in the linker, the DEN MT is rotated toward the RdRp (Fig. 2b,c). Residues Arg363, Gln598 and Asn576 in the fingers subdomain of the ZIKV RdRp interact with the linker to prevent it from being more flexible (Fig. 2d).
Additional interactions between the MT and the RdRp contribute to the orientation of the MT in the ZIKV NS5. In the MT, residues 112–128 that forms Loop 9, α6 and β4 interacts with the α14, Loop 32 and Loop 40 in the RdRp domain (Supplementary Fig. 3). Notably, residues in these structures are highly similar in the NS5 proteins of the ZIKV and JEV, providing an explanation for the similar orientations of the MT and RdRp in these two proteins (Supplementary Fig. 3a). In addition, Loop 32 of the DENV NS5 was disordered, likely contributing to the altered orientation of the MT in the DENV NS5.
The NS5 MTase domain
The MT of ZIKV NS5 adopts a classic α/β/α sandwich structure13. The ZIKV MT can be superimposed with the MTs from other flaviviruses with RMS deviations of <0.73 Å (Fig. 3a). The highly conserved structure allows assignment of the residues that function in RNA cap addition in the ZIKV MT. Residues that bind GTP, catalyse methyl transfer and bind the methyl donor S-adenosyl-methionine (SAM) are arranged in a line within a concave surface of the MT (Fig. 3b,c). The conserved catalytic tetrad of Lys61–Asp146–Lys182–Glu218 that forms the active site is positioned in the centre of the MT (Fig. 3c,d). The putative GTP binding pocket is located to the left of the active site. The SAM-binding pocket is located in a narrow crevice to the right of the catalytic pocket (Fig. 3a,c). SAH, the byproduct of methyl donation from SAM, has the adenylate embedded in a narrow portion of the active site channel, where the Oδ1 of Asp131 forms a H-bond with the N6 of adenine and the Nδ1 of His110 forms a H-bond with the ribose 2′ OH (ref. 7). The homocysteine portion of SAH interacts with loop residues 79–85 (Fig. 3d).
The NS5 polymerase domain
Viral RdRps typically have extensive interactions between the fingers and thumb subdomains to encircle the active site of the polymerase14,15. Three channels are apparent in the ZIKV polymerase. Based on comparison with polymerases whose ternary structures have been determined and characterized16, the channels should bind the template RNA (template channel), guide the emergence of the template and nascent RNA (central channel) and enable the entry of the NTPs (NTP channel) (Fig. 4). Motifs A to G that are conserved in sequence and structure, line the active site cavity and contribute to nucleotide and template recognition and nucleotide polymerization.
The active site of the ZIKV RdRp is enclosed due to the interaction between motifs F and G that project from the fingers to contact the thumb in the front of the RdRp (Fig. 4a,b). The back of the RdRp has a lattice of three loops (Fig. 4a,b). The template RNA will bend at a ca. 45° angle and emerge from the central channel. The NTP channel will merge at the confluence of the template and central channels (Fig. 4b,c). Here three aspartates from motifs C and A (Asp535, Asp665 and Asp666) that coordinate divalent metal ions for nucleotide polymerization are localized. The priming loop, which positions nucleotides for polymerization15, extends from the thumb subdomain is located at the confluence of the three channels (Fig. 4d). In the phage phi6 and HCV RdRp, a tyrosine in the priming element has been shown to form the priming platform by stacking interacting with the initiating nucleotide16,17. In the ZIKV NS5, Trp797 likely performs the role of stacking with first nucleotide to facilitate initiation of de novo RNA synthesis (Fig. 4d).
The RdRp of the hepatitis C virus (HCV), which belongs to the genus Hepacivirus of the Flaviviridae family has been extensively studied for the structures required for de novo initiation and elongation of RNA synthesis18. Residues in the ZIKV RdRp that should contact the RNA and NTPs are located at similar positions to their counterparts in the HCV RdRp ternary complex (Fig. 4e, Supplementary Fig. 4a), suggesting that ZIKV NS5 will have comparable recognition of the template, primer RNA and nucleotides for RNA synthesis. The priming loop of the ZIKV RdRp is larger than that of the HCV RdRp (Supplementary Fig. 4b,c), indicating that conformational changes from the current structure will take place to enable the elongation of the nascent RNA.
MTase interacts with the polymerase to affect RNA synthesis
The MT of the ZIKV NS5 connects to the fingers subdomain of the RdRp and overhangs the NTP channel of the RdRp (Fig. 5a). The MT interacts with the fingers subdomain of the RdRp primarily through a hydrophobic network that involves residues Pro113, Leu115 and Trp121 from the MT and Tyr350, Phe466 and Pro584 from the RdRp (Fig. 5b). The total buried surface area between the MT and the RdRp is ∼1,600 Å2. The close proximity of the MT to the RdRp suggests that the MT may impact RNA synthesis by the RdRp.
To examine whether the interaction of the MT with the RdRp will affect RNA synthesis, we compared the RNA synthesis activity of NS5 to that of a truncated protein, Δ264, which lacks the MT (Supplementary Fig. 5a). The full-length ZIKV NS5 could initiate RNA synthesis de novo or elongate from a primed template in processes that will require distinct RdRp conformations (Fig. 5c, Supplementary Fig. 5b,c). NS5 that had the two aspartates in motif C replaced with alanines was unable to direct RNA synthesis either by de novo initiation or by elongation from a primed template (Supplementary Fig. 5b,c). Δ264 synthesized approximately half of the de novo-initiated RNA product as did full-length NS5 (Fig. 5c, Supplementary Fig. 6). However, with the template that directs elongative RNA synthesis, Δ264 synthesized sevenfold less product than did NS5. Our result demonstrates that the MT contributes to RNA synthesis by the RdRp, especially for elongative RNA synthesis.
The orientation of the MT relative to the template channel and the central channel suggests that it will affect RdRp interaction with the template RNA. A reversible crosslinking, mass spectrometric assay was used to map residues in NS5 that contact the template RNA19. The peptides from NS5 that contacted the RNA were mapped to the template channel, the fingers subdomain and all motifs in the RdRp except for motifs F and D (Fig. 5d, Supplementary Fig. 7a,b). Interestingly, the MT, especially the residues adjacent to the fingers subdomain of the RdRp, also had extensive contact with the template RNA.
Altered RdRp structure in the absence of MTase domain
To better understand the difference in RNA synthesis by NS5 and the RdRp, we determined the crystal structure of Δ264 at 3.0 Å resolution. The asymmetric unit contains eight RdRps that exist in two conformations (referred to as conformation 1 and 2) that vary in the locations of motif G, Loop 21 (residues 312–323) and Loop 51 (residues 742–750) that connect the thumb and fingers subdomains (Fig. 5e). The two conformations are affected by residue Arg483 that lies in the template channel. In conformation 1, the side chain of Arg483 inserts between motifs B and F and interacts with the carbonyl backbone of Gly604 and Trp476 (Fig. 5e, Supplementary Fig. 8a). In conformation 2, the locations of motifs B and F prevents the insertion of the side chain of Arg483. Instead, Arg483 interacts with Ala409 of motif G (Fig. 5e, Supplementary Fig. 8b). Full-length NS5 only has one conformation in the corresponding region and it resembles that of conformation 2 (Fig. 5e, Supplementary Fig. 8c). Notably, motif F in NS5 binds with the MT and has a different conformation relative to that in Δ264 (Fig. 5f). The net effect of the presence of the MT is that the RdRp has a reconfigured template channel and possesses a more open NTP channel (Fig. 5f,g). These changes will likely decrease RNA synthesis.
RNA synthesis by pandemic ZIKV NS5
The current pandemic ZIKV have been observed to be associated with serious human illness1. Strain Brazil/PE243/2015 that was identified from a patient from Recife in Brazil, has more than 35 amino acid substitutions in the NS5 when compared to MR766 (Fig. 6a,b). In terms of RNA synthesis in vitro, NS5 proteins from Brazilian/PE243/2015 and MR766 have comparable activities to direct de novo-initiated and elongative RNA synthesis (Fig. 6c). Mapping of residues changed in the NS5 protein of the Brazil/PE243/2015 onto the MR766 NS5 structure reveals that the substitutions are located on the surface of NS5 and are not involved in the core of the RdRp that can affect RNA synthesis (Fig. 6d).
We have determined the crystal structures of the Zika virus NS5 protein and the isolated polymerase domain. The NS5 protein used was functional for RNA synthesis in vitro, producing RNA that initiated de novo from the 3′ terminal nucleotide of an exogenously provided template and also elongated from a primed template. The MT domain was shown to bind to the template RNA, and its presence increased elongative RNA synthesis by the RdRp domain. The RdRp alone was also competent for RNA synthesis, but was less active for RNA synthesis in vitro (Fig. 5c). This result is in contrast to that of the DENV NS5 protein, where the removal of the MT was shown to increase RNA synthesis in vitro20. However, the NS5 proteins of the ZIKV and the DENV differ in the network of interactions and the orientations of the MT and RdRp domains. These differences may affect RNA synthesis by the resulting recombinant proteins.
The structure of the ZIKV NS5 protein reveals remarkable similarities with the equivalent structures of other viruses from the Flaviviridae family. The active sites for MT activity and RNA synthesis are especially well-conserved. These results suggest that inhibitors of viral MT activity and/or RNA synthesis can be developed to inhibit ZIKV replication. In fact, nucleoside analogues that can inhibit the polymerases of Dengue virus, West Nile virus and yellow fever virus have recently been shown to affect RNA synthesis by ZIKV NS5 (refs 5, 21, 22, 23, 24). Sofosbuvir, which is highly effective in treating hepatitis C, also has modest inhibitory activity for the replication of the ZIKV25. Elucidating additional structures of the ZIKV NS5 complexed to nucleotides and also molecular dynamic studies with the ZIKV NS5 protein with potential inhibitors could aid in the development of inhibitors with higher specificity and potency.
While the Zika virus was initially detected in 1947 in the forest of Uganda Africa, serious illness associated with Zika virus infection was first recorded in Micronesia in 2011 (refs 1, 26). At present, the basis for the increased illness associated with the more recent Zika virus outbreak remains to be established. Our comparison of the recombinant NS5 proteins from Africa and from Brazil revealed similar levels of RNA synthesis. In addition, the residues of the Brazilian ZIKV that differ from those of the MR766 virus from Africa are mostly on the surface of the NS5 protein and are less likely to affect the mechanism of RNA-dependent RNA synthesis. The changes, however, could impact interactions with other ZIKV proteins or with cellular proteins.
SAH was from Sigma and dissolved in H2O. Isopropyl β-D-1-thiogalactopyranoside, imidazole, dithiothreitol, formaldehyde and all other chemicals are from Sigma. Trypsin was purchased from Promega. Ni-NTA resin was from Invitrogen. α-32P-CTP and α-32P-ATP were purchased from PerkinElmer. RNAs were synthesized from Integrated DNA Technologies.
DNA encoding NS5 from ZIKV MR766 (GenBank: NC_012532.1) and Brazilian Zika virus PE243/2015 (GenBank: KX197192.1) were chemically synthesized (Integrated DNA Technologies). The cDNA sequences are in Supplementary Table 1. The cDNA fragment was subcloned into a pET-SUMO vector. The plasmids were transformed into Escherichia coli BL21 Rosetta(DE3) pLysS (Novagen) for protein expression. N-terminal truncations of NS5 that lacked the MT (Δ264) were generated via polymerase chain reaction using the forward primer of the sequence of 5′-ACAGAGAACAGATTGGTGGTGCTGTGGCAAGCTGTGCTGAGGCT-3′ and the reverse primer with the sequence of 5′-CGGATCCGTTATCCACTTTTACAACACTCCGGGTGTGGACCCTTC-3′. Mutations of the RdRp active site were generated via site-directed mutagenesis using the forward primer with the sequence of 5′-CGTATGGCCGTGAGCGGCGCTGCTTGTGTAGTGAAGCCAATTGA-3′ and the reverse primer of the sequence 5′-TCAATTGGCTTCACTACACAAGCAG-CGCCGCTCACGGCCATACG-3′ the QuickChange II kit (Agilent Technologies).
Recombinant protein production and purification
Recombinant proteins were expressed in E. coli Rosetta (DE3) pLys cells (Novagen) grown in Difco LB broth containing ampicillin (50 μg ml−1) and chloramphenicol (17 μg ml−1). When the cultures reached an OD600 of 1.0–1.3, the temperature was reduced to 16 °C, and isopropyl β-D-1-thiogalactopyranoside was added to a final concentration of 0.4 mM. After a 20 h incubation, the bacteria were harvested by centrifugation.
The E. coli cell pellets were suspended in TN buffer (20 mM Tris-Cl pH 8.0, 500 mM NaCl) containing 10 mM imidazole and lysed by sonification. After clarification of the lysate by centrifugation at 15,000g for 30 min, the supernatant was loaded onto a Ni-NTA column that was pre-equilibrated with TN buffer. The column was subsequently washed with TN buffer containing 5 mM β-mercaptoethanol (TNB) and 25 mM imidazole, then TNB buffer containing 40 mM imidazole. The protein was eluted with the TNB buffer containing 350 mM imidazole then exchanged into the TNB buffer containing 20% glycerol. The SUMO-NS5 fusion protein was treated with SUMO protease overnight at 4 °C. NS5 was separated from SUMO and the protease by passage through a second Ni-NTA column. Solutions of NS5 were concentrated and purified with a Superdex200 gel filtration column (GE Healthcare) that was pre-equilibrated with the R buffer (20% glycerol, 20 mM Tris-Cl pH 7.5, 5 mM β-mercaptoethanol) containing 500 mM NaCl. Δ264 that lack the MT was purified using the same protocol except that the Superdex200 column used R buffer containing 150 mM NaCl. All purified proteins were concentrated and stored at −80 °C.
ZIKV NS5 at 5 mg ml−1 and with a 10 molar excess of SAH was used for crystallization. Crystals were grown in 0.1 M bis–tris pH 5.5, 1.0 M ammonium sulfate and 1% (wt/vol) PEG 3350. ZIKV NS5 Δ264 containing the RdRp domain was crystallized in 0.1 M Tris-HCl pH 7.5, 0.2 M sodium citrate tribasic dehydrate and 17% PEG 3350. All proteins were crystallized by hanging-drop vapor-diffusion method at 4 °C. The crystals were flash-frozen in liquid nitrogen in the reservoir solution containing 25% glycerol.
Data collection and structure determination
Diffraction data were collected at beamline 5.0.2 of the advanced light source with a Pilatus 6M detector. The data were processed with iMOSFLM27 and merged with Aimless in the CCP4 package28. The structure of full-length NS5 was determined by molecular replacement using homology models of NS5 MT and RdRp generated with Swiss-model as search models. JEV NS5 structure (PDB 4k6m) was used to generate the homology models. An SAH molecule was docked into the difference map of the MT. The structure of Δ264 was determined by molecular replacement using the homology model of NS5 RdRp as the search model. Phaser in the Phenix package was used for structural determination29. The models were manually adjusted using Coot30 and refined using the Phenix package. Statistics from crystallographic analyses of the two structures are in Table 1. All figures depicting structures were generated using PyMOL (http://www.pymol.org).
In vitro RNA-dependent RNA polymerase assay
RNA synthesis assays were performed in 20 μl of reaction containing 20 mM Tris-HCl (pH 7.8), 100 ng of purified ZIKV protein, 1 mM MnCl2, 5 mM DTT, 0.05% Triton X-100, 10 μM each of ATP, UTP and GTP and 33 nM of α-32P-CTP. Where present, chemically synthesized RNAs DN17 and PE46 (IDT) were, respectively, at 50 and 100 nM. The reactions were incubated at 30 °C for 90 min, then heated for 3 min at 95 °C and loaded directly onto 22% polyacrylamide gels that contained 7.5 M urea and 1/2 × TBE buffer. The gels were separated at 300 V for 3–3.5 h. Radioactive RNA product was detected by a Typhoon Scanner and quantified using ImageQuant software. Radiolabeled RNA markers consisted of chemically synthesized RNAs of 16-, 17- and 18-nt were kinased with γ-32P-ATP. Radiolabeled RNA markers of 19- and 46-nt were produced using the recombinant HCV NS5B as described previously31.
Mapping NS5–RNA interaction
Residues in NS5 that contact RNA were mapped using the reversible crosslinking affinity purification assay19. ZIKV NS5 2 μM were mixed with RNA PE46 RNA (4 μM) and crosslinked with formaldehyde and processed for mass spectrometry. Control reactions were processed in parallel in the absence of formaldehyde. HPLC–MS analysis was conducted on an LTQ Orbitrap XL mass spectrometer equipped with an Accela HPLC and an electrospray ion source (Thermo Scientific). Peptides were eluted over a 90-min gradient, and tandem MS data was acquired using collision-induced dissociation. Peptides were identified using SearchGUI (v3.1.0)32, and searched against a concatenated target/decoy database constructed from the cRAP database (http://www.thegpm.org/crap/index.html) of the sequence of ZIKV NS5. Identification settings included an unspecific protease, 10 p.p.m. MS1, and 0.3 Da MS2 error tolerances and oxidation of methionine as a variable modification. MS2 peptide spectrum matches were inferred using PeptideShaker (v1.13.3)33. Posterior error probability was calculated in PeptideShaker using the ratio of hits from the decoy database relative to the true database search. Only assignments with high confidence and in two independent replicates and those absent in the control reactions were used.
The coordinates for the structure of the full-length ZIKV NS5 have been deposited in the Protein Data Bank under the accession code 5U0B. The coordinates for the structure of the RdRp domain have been deposited in the Protein Data Bank under the accession code 5U0C. The PDB accession codes 4K6M, 4WTL, 3P97, 3ECV, 2OY0 and 5DTO were used in this study. The UniProt accession codes Q32ZE1and ANC90425.2 and the NCBI accession codes NC_012532.1 and KX197192.1 were used in this study. All other data are available from the corresponding authors upon reasonable request.
How to cite this article: Zhao, B. et al. Structure and function of the Zika virus full-length NS5 protein. Nat. Commun. 8, 14762 doi: 10.1038/ncomms14762 (2017).
Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Petersen, L. R., Jamieson, D. J., Powers, A. M. & Honein, M. A. Zika virus. N. Engl. J. Med. 374, 1552–1563 (2016).
Lazear, H. M. & Diamond, M. S. Zika virus: new clinical syndromes and its emergence in the western hemisphere. J. Virol. 90, 4864–4875 (2016).
Lindenbach, B. D., Thiel, H.-J. & Rice, C. M. in Fields Virology 5th edn, (eds Knipe, D. M. et al.) Ch. 33 (Lippincott Williams & Wilkins, 2006).
Egloff, M. P., Bernarroch, D., Selisko, B., Romette, J. L. & Canard, B. An RNA cap (nucleoside-2′-O)-methyltransferase in the flavivirus RNA polymerase NS5: crystal structure and functional characterization. EMBO J. 21, 2757–2768 (2002).
Lim, S. P. et al. Potential allosteric Dengue virus NS5 polymerase inhibitors: mechanism of action and resistance profiling. PLoS Pathog. 12, e1005737 (2016).
Kuno, G., Chang, G. J., Tsuchiya, K. R., Karabatsos, N. & Cropp, C. B. Phylogeny of the genus Flavivirus. J. Virol. 72, 73–83 (1998).
Ray, D. et al. West Nile virus 5′-cap structure is formed by sequential guanine N-7 and ribose 2′-O-methylation by nonstructural protein 5. J. Virol. 80, 8362–8370 (2006).
Issur, M. et al. The flavivirus NS5 protein is a true RNA guanylyl transferase that catalyze a two-step reaction to form the RNA cap structure. RNA 15, 2340–2350 (2009).
Daffis, S. et al. 2′-O methylation of the viral mRNA cap evades host restriction by the IFIT family members. Nature 268, 452–456 (2010).
Ackermann, M. & Padmanabhan, R. De novo synthesis of RNA by the Dengues virus RNA-dependent RNA polymerase exhibits temperature-dependence at the initiation but not the elongative phase. J. Biol. Chem. 276, 39926–39937 (2001).
Kao, C. C., Singh, P. & Ecker, D. J. De novo initiation of viral RNA-dependent RNA synthesis. Virology 287, 251–260 (2001).
van Dijk, A. A., Makeyev, E. V. & Bamford, D. Initiation of viral RNA-dependent RNA polymerization. J. Gen. Virol. 85, 1077–1093 (2004).
Byszewska, M., Smietanski, M., Purta, E. & Bujnicji, J. M. RNA methyltransferases involved in 5′ cap biosynthesis. RNA Biol. 11, 1597–1607 (2014).
Lesburg, C. A. et al. Crystal structure of RNA-dependent RNA polymerase from hepatitis C virus reveals a fully-encircled active site. Nat. Struct. Biol. 6, 937–943 (1999).
Ng, K. K., Arnold, J. J. & Cameron, C. E. Structure-function relationships among RNA-dependent RNA polymerase. Curr. Top. Microbiol. Immunol. 320, 137–156 (2008).
Butcher, S. J., Grimes, J. M., Makeyev, E. V., Bamford, D. H. & Stuart, D. I. A mechanism for initiating RNA-dependent RNA polymerization. Nature 410, 235–240 (2001).
Choi, K. H. et al. The structure of the RNA-dependent RNA polymerase from bovine viral diarrhea virus establishes the role of GTP in de novo initiation. Proc. Natl Acad. Sci. USA 101, 4425–4430 (2004).
Appleby, T. C. et al. Structural basis for RNA replication by the hepatitis C virus polymerase. Science 347, 771–775 (2015).
Vaughan, R. C. & Kao, C. C. Mapping protein-RNA interactions by RCAP, RNA crosslinking and peptide fingerprinting. Methods Mol. Biol. 1297, 225–236 (2015).
Lim, S. P. et al. A crystal structure of the dengue virus non-structual protein 5 (NS5) polymerase delineates interdomain amino acid residues that enhance its thermostability and de novo initiation activities. J. Biol. Chem. 288, 31105–31114 (2013).
Zmurko, J. et al. The viral polymerase inhibitor 7-Deaza-2′-C-methyladenosine is a potent inhibitor of in vitro Zika virus replication and delays disease progression in a robust mouse infection model. PLoS Negl. Trop. Dis. 10, e0004695 (2016).
Morrey, J. D. et al. Efficacy of orally administered T-705 pyrazine analog on lethal West Nile virus infection in rodents. Antivir. Res. 80, 377–379 (2008).
Julander, J. G. et al. Efficacy of 2′-C-methylcytidine against yellow fever virus in cell culture and in a hamster model. Antivir. Res. 86, 261–267 (2010).
Lee, J. C. et al. Characterization of the activity of 2′-C-methylcytidine against dengue virus replication. Antivir. Res. 116, 1–9 (2015).
Retallack, H. et al. Zika virus tropism in the developing human brain and inhibition by azithromycin. Proc. Natl Acad. Sci. USA 113, 14408–14413 (2016).
Duffy, M. R. et al. Zika virus outbreak on Yap Island, Federated States of Micronesia. N. Engl. J. Med. 360, 2536–2543 (2009).
Battye, T. G., Knotogiannis, L., Johnson, O., Powell, H. R. & Leslie, A. G. iMOSFLM, a new graphical interface for diffraction-image processing with MOSFLM. Acta Crystallogr. D Biol. Crystallogr. 67, 271–281 (2011).
Winn, M. D. et al. Overview of the CCP4 suite and current developments. Acta Crystallogr. D67, 235–242 (2011).
Adams, P. D. et al. PHENIX: a comprehensive Python-based system for macromolecular structure solution. Acta Crystallogr. D Biol. Crystallogr. 66, 213–221 (2010).
Emsley, P., Lohkamp, B., Scott, W. G. & Cowtan, K. Features and development of Coot. Acta Crystallogr. D Biol. Crystallogr. 66, 486–501 (2010).
Ranjith-Kumar, R., Gutshall, L., Sarisky, R. T. & Kao, C. Multiple interactions within the hepatitis C virus RNA polymerase repress primer-dependent RNA synthesis. J. Mol. Biol. 330, 675–685 (2003).
Vaudel, M., Barnes, H., Berven, F. S., Sickmann, A. & Martens, L. SearchGUI: an open-source graphical user interface for simultaneous OMSSA and X!Tandem searches. Proteomics 11, 996–999 (2011).
Vaudel, M. et al. PeptideShaker enables reanalysis of MS-derived proteomics data sets. Nat. Biotechnol. 33, 22–24 (2015).
C.C.K. acknowledges seed funding from the Johnson Center for Innovation and Translational Research. We thank Laura Kao for editing the manuscript. 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, of the U.S. Department of Energy under Contract No. DE-AC02-05CH11231.
The authors declare no competing financial interests.
About this article
Cite this article
Zhao, B., Yi, G., Du, F. et al. Structure and function of the Zika virus full-length NS5 protein. Nat Commun 8, 14762 (2017). https://doi.org/10.1038/ncomms14762
Nature Communications (2021)
Frontiers of Medicine (2021)
Science China Life Sciences (2021)
BMC Medicine (2020)
One-step RT-qPCR assay for ZIKV RNA detection in Aedes aegypti samples: a protocol to study infection and gene expression during ZIKV infection
Parasites & Vectors (2020)