Crystal structure analysis, overexpression and refolding behaviour of a DING protein with single mutation

Crystals of a member of the DING protein family (HPBP) were obtained accidentally, and the structure was determined at 1.35 Å resolution. For further analysis, a system for preparation of HPBP was constructed and the structure of a prepared sample was confirmed by X-ray crystal structure analysis at 1.03 Å resolution.


Introduction
DING is a family of proteins with molecular mass of approximately 40 kDa, with a conserved N-terminal sequence of DINGGG. DING proteins have been identified in a wide range of organisms: prokaryotes, animals, fungi and plants (Berna et al., 2008). They have attracted attention due to recent reports that they are involved in many diseases, including rheumatoid arthritis, lithiasis, atherosclerosis, some tumours, tumour-associated cachexia and bacterial and viral infections (Berna et al., 2009;Bookland et al., 2011;Lesner et al., 2009). However, their relevance and/or biological functions have yet to be elucidated. Neither a gene nor ORF encoding DING proteins have yet been identified in eukaryotes despite the high frequency of discovery in eukaryotes (Berna et al., 2008), which has hampered investigation of eukaryotic DING proteins. In contrast, genes of DING proteins have been identified in bacteria (Scott & Wu, 2005).
DING proteins are one of three families within a superfamily of bacterial phosphate-binding proteins (Zhang et al., 2007). To date, the crystal structures of two DING proteins, i.e. human phosphate-binding protein (HPBP) and DING protein from Pseudomonas fluorescens SBW25 (PflDING), have been reported (Morales et al., 2006;Liebschner et al., 2009). In both structures, a phosphate ion was captured in a binding cleft between two domains. For PflDING, a heterologous overexpression system was constructed using Escherichia coli (Scott & Wu, 2005), and the phosphate-binding mode was precisely elucidated based on the sub-angströ m resolution structure of the recombinant PflDING protein (Liebschner et al., 2009). Furthermore, functional analysis was also carried out based on the structural information (Ball et al., 2012). It should be noted that the first crystal of HPBP was accidentally grown from a paraoxonase 1 solution purified from plasma (Morales et al., 2006). From this serendipitous discovery, the authors determined the amino acid sequence by combining the X-ray structure and mass spectrometry (Diemer et al., 2008). Moreover, HPBP was reported to inhibit HIV-1 gene transcription and replication (Cherrier et al., 2011). However, as a system for overexpression has not been reported for HPBP, biochemical experiments such as mutation analysis or domain truncation have not been possible. To gain further understanding of this protein, it is necessary to construct a heterologous overexpression system.
In the present study, HPBP with a single mutation was unexpectedly crystallized during a crystallization trial of a certain protein-RNA complex, as was the case for the first crystal of HPBP. For further analysis of HPBP, an overexpression and refolding system was constructed. The obtained protein was evaluated by X-ray crystallography, and the results indicated that HPBP was correctly refolded to the native structure. To our knowledge, this is the first report of a system for overproduction of HPBP as well as refolding of DING proteins.

Experimental procedures
2.1. Crystallization of HPBP HPBP with single mutation was unexpectedly crystallized during a crystallization trial of a protein-RNA complex. A protein-RNA complex composed of proteins of 53 kDa, 52 kDa and 11 kDa, and its substrate aminoacyl-tRNA were prepared as described previously (Nakamura et al., 2006;Curnow et al., 1997). The purified protein complex and the substrate aminoacyl-tRNA were crystallized and small crystals were grown by the sitting-drop vapour-diffusion method in 100 mM Tris-HCl buffer, pH 8.0, 16% polyethylene glycol 8000, 100 mM NaCl.

Mass spectrometry
Crystals were dissolved in water and then subjected to SDS-PAGE. The band was cut out from the gel and treated with trypsin. The extracted fragments were analysed by LC-MS (LXQ linear ion trap; Thermo Scientific, Waltham, MA, USA) coupled with a Magic2002 (Michrom BioResources, Auburn, CA, USA) and nanospray electrospray ioniser (ESI; AMR, Tokyo, Japan). The determined molecular masses were analysed by Mascot search (Matrix Science, London, UK).

Preparation and crystallization of recombinant HPBP
The amino acid sequence of recombinant HPBP (rHPBP) was determined from the electron density map of the HPBP crystal described above, in which the reported sequence was used as a reference (Morales et al., 2006). The gene of rHPBP synthesized by Genscript (Piscataway, NJ, USA) was cloned into the NcoI and BamHI sites of the pET28b vector (EMD Biosciences, Temecula, CA, USA). A transformed E. coli strain, B834 (DE3), harbouring HPBP expression vector, was grown at 310 K in LB medium until the early stationary phase, and then isopropyl -d-thiogalactopyranoside was added to a final concentration of 0.5 mM to induce expression of the target protein. The culture was grown for an additional 18 h at 298 K. Cells were disrupted using a sonicator (Branson, Danbury, CT, USA) in PBS (100 mM Na 2 HPO 4 , 18 mM KH 2 PO 4 , 137 mM NaCl and 27 mM KCl). The cell lysate was centrifuged at 12000 Â g, 277 K, for 30 min and the insoluble fraction was collected. The inclusion body of rHPBP was purified by re-suspending with PBS containing 0.25% Triton X-100 and centrifugation three times. The obtained inclusion body was rinsed three times with PBS, and stored at 243 K.
The purified inclusion body was solubilized by incubation with denaturing buffer (6 M guanidinium hydrochloride, 20 mM sodium phosphate, pH 8.0, 200 mM NaCl, 2 mM EDTA and 1 mM -mercaptoethanol) for 18 h at room temperature, followed by centrifugation. The unfolded rHPBP was refolded by diluting 1000-fold with refolding buffer (20 mM sodium phosphate, pH 8.0, 200 mM NaCl, 400 mM l-arginine hydrochloride and 1 mM EDTA) followed by incubation with stirring for 18 h at 277 K. After concentrating, the refolded rHPBP solution was dialysed against 20 mM sodium phosphate (pH 8.0), 200 mM NaCl and then 20 mM Tris-HCl (pH 9.0). The soluble fraction was loaded onto a 10 ml HiTrap QXL column (GE Healthcare Bio-Sciences AB, Uppsala, Sweden). The flow-through fraction was collected, and then further purified on a HiLoad 26/60 Superdex 200-pg column (GE Healthcare Bio-Sciences). The purified rHPBP was dialysed against 20 mM HEPES (pH 7.6), 10 mM MgCl 2 , 5% glycerol and 1 mM -mercaptoethanol, and then concentrated to 8.2 mg ml À1 . Crystals of rHPBP were grown in the same conditions under which crystals of HPBP were crystallized as a contaminant.

X-ray diffraction experiments and structure determination
X-ray diffraction patterns of HPBP and rHPBP were obtained on the beamlines BL17A and BL5A, respectively, at the Photon Factory (Tsukuba, Japan). The diffraction data were indexed, integrated, scaled and merged using the XDS package (Kabsch, 2010 Teplyakov, 1997). The structure of rHPBP was determined from the structure of native HPBP. Throughout the refinement in both native HPBP and rHPBP, reflections of the index same as those used for calculation of the R free factor for the reported HPBP structure were used for R free calculation. The positional and individual B-factor refinements were carried out with the program PHENIX (Adams et al., 2010). The structure was modified manually with the program COOT (Emsley & Cowtan, 2004). The R work /R free factors converged to 0.1484/ 0.1696 for native HPBP and 0.1735/0.1840 for rHPBP. The refinement statistics are summarized in Table 1. The coordinates have been deposited in the PDB (IDs 3w9w and 3w9v).

Crystallization and identification of HPBP
We attempted to crystallize a protein complex composed of proteins of 53 kDa, 52 kDa and 11 kDa in complex with its substrate. After crystallization trials and optimization, small crystals were obtained, and a high-resolution X-ray diffraction dataset (1.35 Å resolution) was collected. The crystal belonged to space group C2 with unit-cell parameters a = 94.3 Å , b = 87.1 Å , c = 88.6 Å , = 90.82 . However, the calculated asymmetric unit (727644 Å 3 ) was too small to locate any of the components. The results of SDS-PAGE of these crystals indicated a protein with a molecular mass of approximately 40 kDa that corresponded to none of the target proteins (Fig. 1). To identify the observed protein, it was digested with trypsin and the resultant fragments were analysed by LC-MS. Mascot search of the obtained molecular masses suggested HPBP, a member of the DING protein family, as a candidate. Next, a PDB search was performed for crystal structures with unit-cell parameters similar to those of the obtained crystal. Surprisingly, HPBP (space group C222 1 , a = 96.3 Å , b = 86.8 Å , c = 89.9 Å ) was identified again. It should be noted that the reported HPBP was crystallized as a protein contaminant of paraoxonase 1 purified from human serum (Morales et al., 2006). These observations strongly suggest that the crystal would be HPBP contaminant. Therefore, we attempted to solve the structure by molecular replacement using the reported HPBP (PDB ID 2v3q) as a search model. As expected, the structure was determined (hereafter designated as the native HPBP structure) (Fig. 2a). The clear electron density revealed that the amino acid sequence was identical to that of reported HPBP except for one residue, i.e. Ile211 was substituted by Met (Fig. 2b). As observed for the HPBP reported previously (Morales et al., 2006), a phosphate ion was captured in the binding pocket using T8, L9, S32, D61, R140, S144, G145 and T146 (Fig. 2c).  In addition, two disulfide bonds were formed between Cys113 and Cys158 and between Cys306 and Cys369 (Fig. 2a).

Refolded recombinant HPBP and its structure
To enable further study of DING proteins, an E. coli expression system for HPBP was constructed. The recombinant HPBP (rHPBP) was overexpressed as an insoluble protein (Fig. 3a). Then, the insoluble rHPBP was unfolded with 6 M guanidinium hydrochloride and 1 mM -mercaptoethanol. The chemically unfolded rHPBP was refolded by the dilution method. The refolding efficiency was markedly improved by adding 400 mM l-arginine hydrochloride. The refolded rHPBP was further purified by chromatography, and the final yield was 43 mg per litre of culture.
To evaluate whether rHPBP was refolded correctly, the purified rHPBP was crystallized and its structure was determined. The structure of rHPBP was determined at a resolution of 1.03 Å . The revealed structure was well superposed on the native HPBP with r.m.s.d. of 0.04 Å for 327 C atoms. A phosphate ion was captured at the identical site to native HPBP, with identical residues participating in recognition. Furthermore, two disulfide bonds were formed correctly (Fig. 4). Based on these observations, it was concluded that rHPBP was correctly refolded to the native structure.

Discussion
The crystal structure of contaminating HPBP has been determined twice, i.e. by Morales et al. (2006) and by our group. In addition, the crystal structure of another DING protein was determined at sub-angströ m resolution (0.88 Å ) (Liebschner et al., 2009). These observations suggest that DING proteins may have a strong tendency to crystallize. Furthermore, DING proteins have attracted attention as they were reported to relate to numerous diseases (Berna et al., 2009;Bookland et al., 2011). These observations suggest that DING has the potential for application as crystallizationenhancing fusion protein and/or development of therapeutic agent for some disease as target protein or candidate. However, the nucleotide sequence of eukaryotic DING has not yet been identified and an overexpression system has not been constructed, which has hampered investigation of eukaryotic DING proteins. The present study enabled preparation of rHPBP in very high yield (43 mg per litre of culture). This method is expected to accelerate further study of DING.
Crystals of the refolded rHPBP diffracted to high resolution (1.03 Å ). Although there are many model proteins for X-ray crystallography that can be easily crystallized (e.g. lysozyme and trypsin), there are few refolded proteins which crystallize in high resolution. Therefore, HPBP has potential for application as a model protein for protein science. For this purpose, the outstandingly high yield would be a great advantage. We hope that this report will be helpful for a wide range of research.
The remaining issue to be considered is the source of HPBP. In the present study, the first target proteins were expressed by E. coli. In addition, the substrate aminoacylated-RNA was prepared using enzymes expressed by E. coli. However, no gene corresponding to the HPBP was found in the E. coli SDS-PAGE of rHPBP expressed by Escherichia coli. M is protein marker, P and S represent precipitant and supernatant of recombinant HPBP, respectively.

Figure 4
Crystal structure of refolded rHPBP. Disulfide bonds between Cys113 and Cys158 (a) and Cys306 and Cys369 (b). genome database. Therefore, the possibility of contamination from the expression host was excluded. It should be noted here that the reaction buffer used in order to prepare the substrate aminoacylated-tRNA contained BSA at a concentration of 0.1 mg ml À1 . In the previous case, HPBP was purified from human plasma (Morales et al., 2006). Taken together, it is plausible that HPBP was a contaminant in the BSA used for substrate preparation. However, the reaction solution was treated with phenol after the reaction, and therefore the contaminating HPBP should have been denatured. One probable explanation is that HBPB contaminant in BSA was denatured by phenol after aminoacylation reaction, but the tertiary structure was recovered during the subsequent procedures. This speculation is consistent with the very high yield of refolded rHPBP obtained in the present study.