Crystallization and preliminary X-ray analysis of the GST-fused human Bri3 N-terminal domain

Bri3 is a recently identified proline-rich transmembrane polypeptide up-regulated during TNF-mediated inflammation and immunity. The polyproline-rich N-terminal (residues 1–60) domain of Bri3 was affinity-purified to homogeneity as a glutathione-S-transferase (GST) fusion protein. Crystals were obtained in ∼3 d by the equilibrium vapour-diffusion method from a solution containing 1.5–2.2 M ammonium sulfate and 0.1 M bis-tris pH 6.0. The crystals belong to space group P4₃2₁2, with unit-cell parameters a = b = 91.66, c = 57.53 Å. An X-ray data set was collected to 1.6 Å resolution using synchrotron radiation, with an R_sym of 0.058 and a completeness of 95.3%. There is one molecule of the fusion protein in the asymmetric unit, which corresponds to ∼35% solvent content.

1. Introduction

Tumour necrosis factor-α (TNF) has been implicated in many diseases, such as rheumatoid arthritis, inflammatory bowel disease, cerebral malaria, diabetes, tumours, cardiovascular disease etc. (Aggarwal, 2003). Although the molecular mechanisms of TNF-induced cell death are gradually being unravelled, many genes involved in TNF-induced cell death (Mak & Yeh, 2002) remain unknown. Using suppressed subtractive hybridization from TNF-treated L929 cells, a 125-amino-acid transmembrane protein known as Bri3 has recently been identified (Wu et al., 2003). Bri3 has a proline-rich N-terminal (amino acids 1–65) domain that is predicted not to be associated with the membrane. It has previously been shown that proline-rich regions of polypeptides commonly adopt a left-handed polyproline II (PPII) helical conformation that is very flexible (Creamer & Campbell, 2002). This flexibility poses a great difficulty for the protein to crystallize on its own. However, various studies have shown that the utilization of GST tags (Zhan et al., 2001) and other large affinity tags (Kuge et al., 1997) enhances the solubility of proteins and facilitates crystallization.

As a novel protein overexpressed during TNF-induced cell death, Bri3 is a promising lead for drug discovery. The proline-rich N-­terminal domain of Bri3 containing the PxxP motif can be further explored in order to observe its ability to interact with the SH3 domains of various proteins, as previously shown for other proline-rich sequences (Kaneko et al., 2003; Lewitzky et al., 2004). SH3 domains bind to sequences that adopt a left-handed PPII helical structure in which the two invariant proline residues are found on the same face of the peptide and participate in hydrophobic interactions (Ravi et al., 2004).

The determination of the three-dimensional structure of the proline-rich flexible N-terminal domain region of Bri3 will help to understand its interaction with its various binding partners. It may also shed new light on TNF-induced signalling pathways, which may eventually suggest new strategies for development of new drugs against TNF-related diseases. Here, we describe the crystallization and preliminary X-ray data of the GST-fused Bri3 N-terminal domain (amino acids 1–60), which we will call GST-Bri3N.

2. Cloning protein expression and purification

A construct for GST-Bri3N (amino acids 1–60) was generated from human cDNA using the primers 5′-GCGGATCCGCAATGGACCACAAGCCGCTGCTG-3′ (forward) and 5′-GCGTCGACGTGGATGTTGTAGACCCTGGG-3′ (reverse). The amplified PCR product was ligated into pCR 2.1-TOPO vector (Invitrogen) and subcloned as a BamH1-Sal1 fragment into the BamH1–Sal1 site of pGEX-4T-3. Recombinant GST-Bri3N was expressed in Escherichia coli BL21(DE3) strain. Cells were grown in 1 l Terrific Broth (Bioshop Inc., Canada) medium containing 50 µg ml⁻¹ ampicillin at 310 K to an OD₆₀₀ of 0.8, induced with 0.1 mM isopropyl-β-D-thiogalactopyranoside and grown for 4 h at room temperature. The cells were harvested and stored at 253 K until further use. Lysis was performed in PBS buffer (140 mM NaCl, 2.7 mM KCl, 10 mM Na₂HPO₄, 1.8 mM KH₂PO₄) pH 7.3 containing 1 mM phenylmethanesulfonyl fluoride, 10 mM dithiotheritol and 0.1 mg ml⁻¹ DNAse I using three cycles of brief sonication for 20 s pulsed with a 5 min gap between each cycle. The lysate was cleared by centrifugation and loaded onto a GSTrap column (Pharmacia) for affinity purification using the glutathione-S-transferase (GST) tag attached to the protein. After multiple washes with PBS, GST-Bri3N was eluted using 50 mM Tris–HCl containing 10 mM reduced glutathione pH 8.0 and was then purified to homogeneity by AKTA FPLC using Sepharose G-75 (16/60) size-exclusion column chromatography. The single peak was pooled and concentrated to 36 mg ml⁻¹. The presence of Bri3 in the GST-fused protein was confirmed by cleavage of the GST tag using one unit of thrombin (Sigma) per milligram of fusion protein. The cleavage product was run on a 20% Tris–tricine gel as described previously (Schagger & von Jagow, 1987). Fig. 1 shows a single band corresponding to Bri3N cleaved from GST-tagged fusion protein.

Figure 1 Tris–tricine polyacrylamide gel showing the cleavage of Bri3N from GST-fusion protein.

3. Crystallization

GST-Bri3N was dialyzed into 10 mM phosphate buffer pH 7.0 for crystallization and concentrated to 10 mg ml⁻¹. The flowthrough from the concentrator was used as a negative control for crystallization. Initial crystallization trials for GST-Bri3N were performed using the equilibrium vapour-diffusion (hanging-drop) method at room temperature (293 K). Drops containing 2 µl protein sample (10 mg ml⁻¹) and 2 µl mother liquor were equilibrated against 1 ml reservoir solution. Sparse-matrix screens (Hampton Research) were performed as initial trials and the lead conditions were refined. The final condition contained 1.5–2.2 M ammonium sulfate and 0.1 M bis-tris pH 6.0. The crystals reached maximum dimensions of ∼0.3 × 0.3 × 0.2 mm (Fig. 2) within 3 d.

Figure 2 Typical GST-Bri3N crystal of approximate dimensions 0.3 × 0.3 × 0.2 mm.

4. X-ray data collection

Data collection was carried out at the X6A station of Brookhaven National Laboratory using an ADSC Quantum 210 CCD detector at a wavelength of 0.9795 Å. Prior to data collection at 100 K, crystals were soaked in crystallization buffer containing 20%(v/v) PEG 400 for 2–­3 min, followed by flash-cooling in a gas stream of liquid nitrogen. All data were processed with DENZO and SCALEPACK (Otwinowski & Minor, 1997). The crystals belong to space group P4₃2₁2, with unit-cell parameters a = b = 91.66, c = 57.53 Å. Crystals diffracted well and a data set was collected to 1.6 Å resolution, with an R_sym of 0.058 and a completeness of 95.3% (Table 1). There is one GST-Bri3N molecule in the asymmetric unit, which corresponds to ∼35% solvent content.

Table 1
Statistics of X-ray diffraction data

Values in parentheses are for the highest resolution shell.

Space group	P43212
Unit-cell parameters (Å)	a = b = 91.66, c = 57.53
No. measured reflections	251419
No. independent reflections	30981
Resolution range (Å)	30.0–1.6 (1.66–1.60)
Rsym† (%)	5.8 (29.7)
Completeness (%)	95.3 (73.2)
Average I/σ(I)	38.1 (2.7)

†R_sym = , where I(k) and 〈I〉 represent the diffraction intensity values of the individual measurements and the corresponding mean values. The summation is over all measurements.

Molecular replacement using a GST probe structure (PDB code 1bg5 ) was successful in space group P4₃2₁2. We are in the process of locating BRI3 density in order to achieve structure determination of the entire fusion protein.

Footnotes

‡These authors made equal contributions.