Contribution of intertwined loop to membrane association revealed by Zika virus full‐length NS1 structure (original) (raw)

Abstract

The association of Zika virus (ZIKV) infections with microcephaly and neurological diseases has highlighted an emerging public health concern. Here, we report the crystal structure of the full‐length ZIKV nonstructural protein 1 (NS1), a major host‐interaction molecule that functions in flaviviral replication, pathogenesis, and immune evasion. Of note, a long intertwined loop is observed in the wing domain of ZIKV NS1, and forms a hydrophobic “spike”, which can contribute to cellular membrane association. For different flaviviruses, the amino acid sequences of the “spike” are variable but their common characteristic is either hydrophobic or positively charged, which is a beneficial feature for membrane binding. Comparative studies with West Nile and Dengue virus NS1 structures reveal conserved features, but diversified electrostatic characteristics on both inner and outer faces. Our results suggest different mechanisms of flavivirus pathogenesis and should be considered during the development of diagnostic tools.

Synopsis

The Zika virus (ZIKV) nonstructural protein 1 (NS1) functions in viral replication, pathogenesis, and immune evasion. Here, we solved the crystal structure of full‐length NS1 protein, and found an extended membrane association interface contributed by the hydrophobic “spike” of a long intertwined loop, providing important information for ZIKV pathogenesis and development of diagnostic tools.

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Introduction

Zika virus (ZIKV) has caused global concern, as growing clinical and experimental evidence showed that ZIKV infection is highly associated with microcephaly and serious neurological complications such as Guillain–Barré syndrome (GBS), even though ZIKV was previously considered a mild pathogen for humans (Cao‐Lormeau et al, 2016; Carteaux et al, 2016; Mlakar et al, 2016; Ventura et al, 2016; Wang et al, 2016; Zhang et al, 2016; Zhu et al, 2016). ZIKV belongs to Flaviviridae family and has a single‐strand positive‐sense RNA genome (Musso & Gubler, 2016). ZIKV can be transmitted by mosquitoes of the genus Aedes, and recently, several clinical investigations showed that it can also be transmitted by sexual contact (Ledermann et al, 2014; Musso et al, 2015; D'Ortenzio et al, 2016). To date, there are no clinically approved vaccines or antiviral drugs available to protect or treat ZIKV infections. To help accelerate the development of specific medical countermeasures, more studies are needed to understand the pathogenesis of ZIKV.

First described as a soluble complement fixing (SCF) antigen more than four decades ago (Brandt et al, 1970; Russell et al, 1970), the unusual properties of the flavivirus nonstructural protein 1 (NS1) have puzzled the flavivirus research field. NS1 protein is involved in many steps of the flavivirus life cycle, including viral replication, immune evasion, and pathogenesis (Amorim et al, 2014). It is thought that the glycosylated NS1 protein, which associates with lipids, forms a homodimer inside the cells, and separates into three distinct populations: a significant population participates in the viral replication complex, a second minor population is trafficked to the plasma membrane, and the third is secreted into the extracellular space as a hexameric lipoprotein particle (Flamand et al, 1999; Gutsche et al, 2011; Muller et al, 2012). Structural studies of dengue virus (DENV) and West Nile virus (WNV) NS1 have revealed the architecture of dimeric and hexameric NS1 proteins, providing molecular insight into the NS1 structure–function relationships (Akey et al, 2014). Recently, we have solved the C‐terminal region of ZIKV NS1 protein and elucidated a differential electrostatic potential in the host‐interaction interface, compared with other flavivirus proteins with known structures (Song et al, 2016a). However, molecular information about the full‐length ZIKV NS1 remains unknown.

Here, we have solved the crystal structure of full‐length ZIKV NS1, and found that the overall structural fold is similar to other flavivirus NS1 structures, including DENV and WNV. Importantly, a long intertwined loop was observed in the wing domain of ZIKV NS1, forming a hydrophobic “spike”. This hydrophobic “spike” can contribute to the membrane association of ZIKV NS1, together with the β‐roll and connector subdomain. Further sequence analysis revealed that the “spike” sequences of different flavivirus NS1 proteins are variable but have common features, consisting of hydrophobic or positively charged amino acids, which is beneficial for cellular membrane association. Moreover, ZIKV NS1 has unique electrostatic potential maps on both inner and outer faces, which might lead to interaction with host proteins different from those used by DENV and WNV NS1. Our results suggest that ZIKV pathogenesis may be distinct from other flaviviruses and should be considered in the development of specific diagnostic antigens.

Results

Overall structure of ZIKV full‐length NS1

We expressed the full‐length ZIKV NS1 (residues 2–352, BeH819015 strain isolated from Brazil in 2015) in insect cells using the baculovirus expression system, following the construct as previously reported (Brown et al, 2011). The recombinant NS1 protein was successfully purified and crystallized in 0.1 M Tris–HCl pH 8.5, 2.0 M ammonium sulfate, and then, we determined its X‐ray structure at 2.85 Å by molecular replacement using DENV NS1 structure (PDB ID: 4O6B) (Akey et al, 2014) as a search model (Table 1). The structure is complete for all amino acid residues, especially containing the internal loop (amino acids 108–128), which is not observed in either of the WNV or DENV2 structures. There are two potential N‐linked glycosylation sites (N130 and N207), and N207 is seen to be glycosylated with one sugar residue in clear electron density in our ZIKV NS1 structure. This observation of little carbohydrate does not reflect the real situation, and our insect cell‐produced NS1 protein would have simpler glycosylation than the mammalian cell‐produced NS1 protein. These two glycosylation sites are highly conserved for different flaviviruses.

Table 1 Data collection and refinement statistics

Full size table

The overall structure of ZIKV NS1 protein is very similar to WNV and DENV2 NS1 structures (0.84 and 0.74 Å root mean square deviation (rmsd), respectively, of 539 Cα atoms). The ZIKV NS1 dimer is organized around an extended central β‐sheet domain, and each monomer has three domains, β‐hairpin domain, wing domain, and β‐ladder domain (Fig 1A). The first β‐hairpin domain (amino acids 1–30) forms a mini domain‐swap structure together with the β‐hairpin domain of the other NS1 monomer in the NS1 dimer structure, and these two β‐hairpin domains intertwine in a roll‐like structure, designated as “β‐roll” dimerization domain. The wing domain (amino acids 31–181) of each monomer protrudes from the central β‐ladder domain, containing one glycosylation site (N130) and two subdomains. An α/β subdomain (amino acids 38–151) consists of a four‐stranded β‐sheet, two α‐helices and a long intertwined loop between β5‐ and β6‐strands (amino acid residues 91–130) (Fig 1A and B). A discontinuous connector subdomain (amino acid residues 30–37 and 152–180) connects the wing domain to the central β‐roll and β‐ladder domains (Fig 1A and B). The predominant structural feature of NS1 is the third domain, a continuous β‐ladder domain (amino acid residues 182–352), extending along the length of the dimer with its 10 β‐strands (Fig 1A and B). The β‐ladder domains from two NS1 monomers from a long β‐sheet with 20 β‐strands arranged like the rungs of a ladder (Fig 1A). In the β‐ladder domain, most of the interstrand loops are short, except a long “spaghetti loop” between β13 and β14 that lacks repetitive secondary structures (such as α‐helix or β‐strand) but is ordered by extensive hydrogen bonds (Fig 1C, cyan). The β‐ladder domain of each monomer can be separated into two parts by the “spaghetti loop”, the central region containing the first four β‐strand rungs and the tip region containing the remaining six β‐strand rungs (Fig 1B).

Figure 1

Overall structure of ZIKV NS1 dimer and extended surface for membrane association

A. NS1 dimer with one subunit in gray and the other colored by domain (green, β‐roll; orange, wing with magenta connector subdomain; blue, central β‐ladder). N‐linked glycosylation sites are shown in sticks, and the glycans are shown in spheres.

B. Topology diagram for the NS1 monomer, colored as the pattern in (A). Glycosylation sites are indicated with red hexagons and disulfide bonds with yellow circles.

C. Side views of the NS1 dimer from the wing (left) and the end of the β‐ladder (right). The β‐roll (green), connector subdomain (magenta), and the intertwined loop (yellow) of the wing domain (orange) form a discontinuous protrusion on one face of the β‐ladder with the spaghetti loop (cyan) on the other face. The wing domain is omitted from the left image for clarity.

The overall dimensions of the ZIKV NS1 dimer are 85 Å along the β‐ladder, 95 Å in width from wingtip to wingtip, and 35 Å in the third dimension (Fig 1A). The β‐ladder defines a plane with the β‐roll domain and the second half part of intertwined loop of the wing domain on one side, and on the other side of the plane are the “spaghetti loop”, the N130‐glycosylation site, the first half part of intertwined loop of the wing domain and the C‐terminus, which is fused to the lumen‐side N terminus of viral protein NS2A before proteolytic cleavage (Fig 1C).

Intertwined loop may contribute to membrane association of ZIKV NS1

The β‐roll, the connector subdomain, and the second half part of the intertwined loop of the wing create a discontinuous linear hydrophobic protrusion with a markedly hydrophobic surface on the inner side of the dimer (Fig 1C). This hydrophobic surface is mainly constituted by aromatic residues such as F8, Y122, F123, F163, and H164 (Fig 1C). This “hydrophobic protrusion” provides a perfect interface to associate with the hydrophobic‐lipid membrane surface, and orients the outer hydrophilic face of the dimer toward the lumen, and subsequently the extracellular space. Previous work on WNV NS1 showed that the residues at the β‐roll (10–11 on a β‐turn) are implicated in a direct interaction with NS4B (Youn et al, 2012), implying the membrane surface interacting with other proteins of the replication complex. Residues in the connector subdomain (159–162 on a β‐turn) are also shown to be important for viral replication (Akey et al, 2014). In our ZIKV NS1 structure, we can clearly see the second half part of the intertwined loop of the wing, which exists between the β5 and β6 strands, clearly. This long loop (consists of Y122, F123, V124) forms a hydrophobic “spike” that may associate with the membrane. This exposed loop is considered to be critical in mediating NS1 interaction with the envelope protein, thus tethering the replication complex with virion formation (Scaturro et al, 2015).

In addition, we have modeled the ZIKV hexamer structure based on that previously reported for DENV2 NS1 (Fig 2). We found that the intertwined loop “spike” of one monomer has a very close distance to the β‐ladder domain of the neighboring NS1 monomer (Fig 2), indicating that the intertwined loop probably participates in the formation of the ZIKV NS1 hexamer. The modeled ZIKV NS1 hexamer reveals a hydrophobic hole surrounded by the “inner” faces of three NS1 dimers, containing the β‐roll domain and the intertwined loop “spike” (Fig 2). By contrast, the “outer” faces can be easily bound by host factors and reactive antibodies.

Figure 2

Model of the ZIKV NS1 hexamer

The ZIKV NS1 hexamer is modeled by using the full‐length DENV2 NS1 structure (PDB code: 4O6B) (Akey et al, 2014). Each monomer is colored by domains (green, β‐roll; orange, wing; magenta, connector subdomain; blue, central β‐ladder). The intertwined loop “spike” of ZIKV NS1 contributing to membrane association is colored in red and indicated by dotted lines.

Comparison with other flavivirus NS1 structures

We compared the ZIKV NS1 structure with the available NS1 structures of DENV2 and WNV (Akey et al, 2014). Previously, we found that the electrostatic surface potential maps of these NS1 proteins have group‐specific features in the loop surface of the β‐ladder domain (Song et al, 2016a). The DENV2 NS1 structure displays a positively charged surface in the central region of the loop surface, whereas the WNV NS1 structure has a negatively charged central region. For ZIKV, the loop surface exhibits a composite surface containing both a positively and negatively charged central region and displays a negatively charged region toward the two distal ends (Fig 3). Interestingly, in the “inner” face with the β‐roll domain, only ZIKV displays negatively charged surface, whereas DENV2 and WNV display surfaces of neutral charge. Moreover, we have observed different features in the “outer” face of the wing domain. ZIKV NS1 displays a positively charged surface in the tip region of the wing domain, whereas the WNV NS1 structure has a negatively charged region, and the DENV2 NS1 structure contains both positively and negatively charged regions (Fig 3).

Figure 3

Variation in electrostatic surface potential of flavivirus NS1 proteins

A–C Electrostatic surface views of NS1 from DENV2 (PDB: 4O6B, A) and WNV (PDB: 4O6C, B) (Akey et al, 2014), as well as ZIKV (C), showing diverse characteristics on certain regions. Surfaces are colored by electrostatic potential at neutral pH from −2 kT (red) to +2 kT (blue) using PyMOL (http://pymol.org/).

Conserved features of NS1 sequences relating to their structure–function relationships

In Fig 4A, the NS1 surface is colored according to sequence conservation from the most conserved (dark magenta) to the most divergent (dark cyan) based on an alignment of NS1 sequences from 73 flaviviruses (Fig 4A and Table EV1). The most conserved surfaces are on the β‐roll region and the C‐terminal tip of the central β‐ladder. The “outer” face of the wing domain is the most variable region. For the protruding tip (residues 122–124) of the intertwined loop, the amino acid sequence is variable (Fig 4B). Irrespective of amino acid variations, these residues are always hydrophobic or positively charged, which is beneficial for membrane association (Figs 5 and EV1).

Figure 4

NS1 sequence conservation mapped onto the protein surface and models of membrane association for ZIKV, WNV and DENV2

A. The NS1 surface is colored using the ConSurf server (Ashkenazy et al, 2016) according to sequence conservation from the most conserved (dark magenta) to the most divergent (dark cyan) based on an alignment of NS1 sequences from 73 flaviviruses.

B. Models of intertwined loop “spike” interacting with the cellular membrane. The disordered “spike” regions are indicated by dash lines in DENV2 and WNV NS1 structures, which consist of hydrophobic or positively charged amino acids.

Figure 5

Detailed analysis of the intertwined loop in the wing domain of ZIKV NS1 structure

A. B‐factor putty representation of the intertwined loop structure. Shades of blue and a narrower tube indicate regions with lower B‐factors, whereas orange to red and a wider tube indicate regions with higher B‐factors. The figure was prepared using PyMOL (http://pymol.org/).

B. The 2Fo‐Fc electron density map for the intertwined loop (yellow) “spike” region residues contoured at 1.0 sigma is represented in blue.

C. Detailed interactions of the highly conserved residues W115 and W118 with the neighboring residues to stabilize the conformation of the intertwined loop. W115 forms a hydrogen‐bonding interaction with E74 from α2‐helix. W118 inserts into the hydrophobic interspace between α1‐ and α2‐helix, formed by P36, L42, V71, L75, and I78, and W118 also interact with P36 and D37 by hydrogen‐bonding interactions.

D. Sequence alignment of the intertwined loop region (residues 91–130) of different flavivirus NS1 proteins. The intertwined loop “spike” residues of ZIKV NS1 contributing to membrane association are indicated by a dark blue arrowhead. Accession codes: ZIKV strain BeH819015, AMA12085; West Nile virus (WNV), Q9Q6P4; Dengue virus 1 Nauru/West Pac/1974 (DENV1), P17763; Dengue virus 2 Puerto Rico/PR159‐S1/1969 (DENV2), P12823; Dengue virus 3 Singapore/8120/1995 (DENV3), Q5UB51; Dengue virus 4 Thailand/0348/1991 (DENV4), Q2YHF0; Japanese encephalitis strain K94P05 (JEV), AAC02714; St. Louis encephalitis (SLEV), D8L537; Yellow fever 17D vaccine strain (YFV), CAA27332; Murray Valley encephalitis (MVEV), NP_051124; Tickborne encephalitis (TBEV), NP_043135.

The “outer” face has been suggested to play a crucial role in interactions of NS1 with host factors and antibodies (Chung et al, 2006a,b; Avirutnan et al, 2007; Edeling et al, 2014). A wide range of host proteins present on platelets and endothelial cells have been identified as cross‐reactive targets by NS1‐induced autoantibodies (Sun et al, 2007, 2015; Cheng et al, 2009; Chuang et al, 2011, 2014; Liu et al, 2011; Yin et al, 2013). ZIKV NS1 displays an interface with variable surface and divergent electrostatic potential that may result in altered binding properties to host factors and protective antibodies against flavivirus NS1.

Discussion

As the only viral protein which can be secreted into the extracellular space, the nonstructural protein NS1 plays diverse roles in immune evasion via binding to complement proteins and modifying or antagonizing their functions (Chung et al, 2006a; Avirutnan et al, 2010, 2011). NS1 was also shown to activate Toll‐like receptor 4 signaling in primary human myeloid cells, leading to secretion of pro‐inflammatory cytokines and vascular leakage (Beatty et al, 2015; Modhiran et al, 2015). Besides its immune evasive and endothelial permeability functions, NS1 modulates early events in viral RNA replication (Watterson et al, 2016). Indeed, deletion of NS1 completely abrogates viral RNA replication, but ectopic expression of NS1 in trans can efficiently rescue NS1‐deleted viruses (Lindenbach & Rice, 1997; Khromykh et al, 2000). It is thought that membrane‐associated NS1 dimer on the luminal face of the endoplasmic reticulum (ER) membrane plays an essential organizational role in the formation of the replication complex through interaction with NS4A and NS4B (Lindenbach & Rice, 1999; Youn et al, 2012). NS1 has also been proposed to interact with prM and the envelope protein, linking replicative complexes within the vesicle packets together with virion formation (Scaturro et al, 2015). In our ZIKV NS1 structure, we found that the intertwined loop “spike”, between the β5 and β6 strands of the wing domain, containing hydrophobic residues Y122, F123, and V124, forms an extended hydrophobic protrusion together with the β‐roll and the connector subdomain, and most likely involves in association with the membrane surface. It is intriguing that this intertwined loop is disordered in the previously reported DENV2 and WNV NS1 crystal structures. We speculate two possibilities for the discrepancy: First, we have further analyzed the crystal contacts of the intertwined loop in our ZIKV NS1 structure, and indeed found that the crystal packing can help stabilize the conformation of this intertwined loop; second, the different protein purification methods (the DENV2 and WNV NS1 proteins were purified with detergent) may also affect the conformation of the hydrophobic intertwined loop, as the detergent molecules could bind to the intertwined loop. Detailed analysis revealed that the intertwined loop does not have higher B‐factors (temperature factors) than the rest of the ZIKV NS1 structure, and is observed in the clear electron density map (Fig 5A and B), indicating that this loop is relatively stable in our structure. Moreover, highly conserved residues W115 and W118 could further stabilize the conformation of the intertwined loop by interaction with the neighboring residues (Fig 5C and D). Janet Smith and her colleagues recently reported the full‐length NS1 structure from the original 1947 Ugandan ZIKV strain (MR766). The structure is similar to that reported here, including an elongated hydrophobic region for membrane association in the wing domain, highlighting the importance of the intertwined loop (Brown et al, [2016](/article/10.15252/embj.201695290#ref-CR500 "Brown WC, Akey DL, Konwerski JR, Tarrasch JT, Skiniotis G, Kuhn RJ, Smith JL (2016) Extended surface for membrane association in Zika virus NS1 structure. Nat Struct Mol Biol 23: 865–867 ‡Correction added on 17 October 2016, after first online publication: the reference Brown et al (2016) has been added to the reference list.

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From the conservation analysis of all the flavivirus NS1 sequences mapped onto the protein surface, we found that the hydrophobic protrusion and the C‐terminal tip of the central β‐ladder regions are most conserved, while the “outer” face of the wing domain are most variable, indicating the latter has divergent characteristics among different flaviviruses. The electrostatic surface potential of that region in ZIKV NS1 also shows specific features compared with that of DENV2 and WNV NS1 structures. The unique surface characteristics of ZIKV NS1 may be related to ZIKV neurotropism and could be exploited in the development of novel therapeutic and diagnostic tools for ZIKV infection (Stettler et al, 2016).

The high level of secreted NS1 in the blood of flavivirus‐infected individuals during early infection has made NS1 a primary biomarker in disease diagnosis (Alcon et al, 2002). In addition, NS1 is a potential vaccination candidate against flavivirus infection (Amorim et al, 2014). Immunization of mice with DENV NS1 was protective against subsequent lethal DENV challenge (Schlesinger et al, 1987). However, autoantibodies against NS1 can elicit severe autoimmune diseases (Cheng et al, 2009; Chuang et al, 2011). More recently, a panel of monoclonal antibodies from ZIKV‐infected patients was isolated, and most of the antibodies were ZIKV‐specific, and memory T cells against NS1 proteins were poorly cross‐reactive, even in donors pre‐exposed to DENV, indicating that the ZIKV NS1 protein could induce a prominent ZIKV‐specific immune response (Stettler et al, 2016). Their results support our data that the ZIKV NS1 structure has unique surface characteristics, which has implications for developing a serological diagnostic tool against ZIKV NS1. Further research should focus on characterizing the diverse epitopes within NS1 for eliciting auto‐ or protective antibodies.

Materials and Methods

Gene cloning, expression, and protein purification

The ZIKV NS1 construct (amino acid residues 2–352, Accession Number: AMA12085) was cloned into the baculovirus transfer vector pFastBac Dual (Invitrogen) under control of the polyhedrin promoter, in‐frame with an N‐terminal gp67 signal peptide for secretion and a His6‐tag at the N‐terminus for purification. We placed green fluorescent protein (GFP) under control of the P10 promoter to visualize expression, which correlated well with expression of NS1. Recombinant pFastBac Dual plasmid was used to transform DH10Bac™Escherichia coli (Invitrogen). Transfection and virus amplification were performed according to the Bac‐to‐Bac baculovirus expression system manual (Invitrogen) (Song et al, 2016b). NS1 proteins were produced by infecting suspension cultures of Hi5 cells (Invitrogen) for 2 days. Soluble NS1 was recovered from cell supernatants by metal affinity chromatography using a HisTrap HP 5 ml column (GE Healthcare), and then purified by ion‐exchange chromatography using a RESOURCE™Q 6 ml column (GE Healthcare). For crystallization, the proteins were further purified by gel filtration chromatography using a Hiload 16/60 Superdex® 200 PG column (GE Healthcare) with a running buffer of 20 mM Tris–HCl and 50 mM NaCl (pH 8.5), and the collected protein fractions were concentrated to 10 mg/ml using a membrane concentrator with a molecular weight cutoff of 10 kDa (Millipore).

Crystallization, data collection, and structure determination

The initial screening trials were set up with commercial crystallization kits (Hampton Research and Molecular Dimensions) using the sitting‐drop vapor diffusion method with a Mosquito® LCP crystal screening robot (TTP Labtech). Normally, 0.5 μl protein was mixed with 0.5 μl reservoir solution. The resultant drop was then sealed, equilibrating against 70 μl reservoir solution at 4 or 18°C. Diffractable crystals were obtained in 0.1 M Tris–HCl pH 8.5, 2.0 M ammonium sulfate. Crystals were flash‐cooled in liquid nitrogen after a brief soak in reservoir solution with the addition of 17% (v/v) glycerol. X‐ray diffraction data were collected under cryogenic conditions (100 K) at the wavelength 0.97853 Å at Shanghai Synchrotron Radiation Facility (SSRF) beamline BL17U, and indexed, integrated, and scaled with HKL2000 (Otwinowski & Minor, 1997).

The ZIKV NS1 structure was solved by the molecular replacement method using Phaser (Read, 2001) from the CCP4 program suite (Winn et al, 2011), with the structure of DENV2 NS1 (PDB: 4O6B) as the search model (Akey et al, 2014). Initial restrained rigid‐body refinement and manual model building were performed using REFMAC5 (Murshudov et al, 1997) and COOT (Emsley & Cowtan, 2004), respectively. Further refinement was performed using Phenix (Adams et al, 2010). Final statistics for data collection and structure refinement are represented in Table 1.

Notes

  1. †Correction added on 17 October 2016, after first online publication: the last two sentences in this paragraph have been added.
  2. ‡Correction added on 17 October 2016, after first online publication: the reference Brown et al ([2016](/article/10.15252/embj.201695290#ref-CR500 "Brown WC, Akey DL, Konwerski JR, Tarrasch JT, Skiniotis G, Kuhn RJ, Smith JL (2016) Extended surface for membrane association in Zika virus NS1 structure. Nat Struct Mol Biol 23: 865–867
    ‡Correction added on 17 October 2016, after first online publication: the reference Brown et al (2016) has been added to the reference list.

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Acknowledgements

This work was supported by the Emergency Task‐Force Project (Grant No. 81641001) of the National Natural Science Foundation of China (NSFC), the China Ministry of Science and Technology (MOST) National 973 Project (Grant No. 2014CB542503), the Task‐Force of Zika Virus Research from the Chinese Academy of Sciences (CAS), the National Key Plan for Scientific Research and Development of China (2016YFD0500300), Zika Special Project of the MOST Reform and Development Project, and Strategic Priority Research Program of the Chinese Academy of Sciences (XDB08020100). We thank the staff of beamline BL17U at Shanghai Synchrotron Radiation Facility, for assistance during data collection. Y.S. is supported by the Excellent Young Scientist Program from the NSFC (No. 81622031), the Excellent Young Scientist Program of the Chinese Academy of Sciences and the Youth Innovation Promotion Association CAS (2015078). G.F.G. is supported partly as a leading principal investigator of the NSFC Innovative Research Group (Grant No. 81321063).

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  1. These authors contributed equally to this work

Authors and Affiliations

  1. School of Life Sciences, University of Science and Technology of China, Hefei, China
    Xiaoying Xu & George F Gao
  2. CAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China
    Xiaoying Xu, Hao Song, Jianxun Qi, Yuqian Liu, Haiyuan Wang, Chao Su, Yi Shi & George F Gao
  3. Research Network of Immunity and Health (RNIH), Beijing Institutes of Life Science, Chinese Academy of Sciences, Beijing, China
    Hao Song & George F Gao
  4. Savaid Medical School, University of Chinese Academy of Sciences, Beijing, China
    Jianxun Qi, Yi Shi & George F Gao
  5. Institute of Health Sciences, Anhui University, Hefei, China
    Yuqian Liu
  6. College of Animal Sciences and Technology, Guangxi University, Nanning, China
    Haiyuan Wang
  7. College of Veterinary Medicine, China Agricultural University, Beijing, China
    Chao Su
  8. Center for Influenza Research and Early‐warning (CASCIRE), Chinese Academy of Sciences, Beijing, China
    Yi Shi & George F Gao
  9. National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention (China CDC), Beijing, China
    George F Gao

Authors

  1. Xiaoying Xu
  2. Hao Song
  3. Jianxun Qi
  4. Yuqian Liu
  5. Haiyuan Wang
  6. Chao Su
  7. Yi Shi
  8. George F Gao

Contributions

GFG and YS designed and supervised the study. XX, HS, YL, HW, and CS conducted the experiments. JQ collected the data sets and solved the structures. YS, HS, and GFG analyzed the data and wrote the manuscript.

Corresponding authors

Correspondence toYi Shi or George F Gao.

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The authors declare that they have no conflict of interest.

Additional information

See also: R Hilgenfeld (December 2016)

The EMBO Journal (2016) 35: 2170–2178

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Xu, X., Song, H., Qi, J. et al. Contribution of intertwined loop to membrane association revealed by Zika virus full‐length NS1 structure.EMBO J 35, 2170–2178 (2016). https://doi.org/10.15252/embj.201695290

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