Received 31 May 2006
Purification, crystallization and preliminary X-ray diffraction analysis of RafE, a sugar-binding lipoprotein from Streptococcus pneumoniae
aDepartment of Chemistry and WestCHEM, Glasgow Biomedical Research Centre (GBRC), University of Glasgow, 120 University Place, Glasgow G12 8TA, Scotland, and bDivision of Infection and Immunity (IBLS), Glasgow Biomedical Research Centre (GBRC), University of Glasgow, 120 University Place, Glasgow G12 8TA, Scotland
Streptococcus pneumoniae contains a large number of sugar-transport systems and the system responsible for raffinose uptake has recently been identified. The substrate-binding protein component of this system shares strong sequence homology with the multiple sugar metabolism substrate-binding protein MsmE from S. mutans and contains a lipoprotein-attachment site at cysteine residue 23. A truncated form (residues 24-419) of RafE from S. pneumoniae was cloned and overexpressed in Escherichia coli. Native and selenomethionine-labelled protein have been crystallized in the hexagonal space group P6122. Diffraction data have been successfully phased to 2.90 Å using Se SAD data and model building is in progress.
Streptococcus pneumoniae is a major human pathogen that mainly affects the young, elderly and immunocompromized populations. Pneumococcal infection is estimated to kill over one million children under the age of five annually, with the majority of these deaths occurring in developing countries (World Health Organization, 1999).
Genomic analysis of S. pnemoniae TIGR4 reveals a high level of carbohydrate utilization in comparison to other species (Haemophilus influenzae and Neisseria meningitidis) that colonize the human upper respiratory tract (Tettelin et al., 2001). Over 30% of the transport systems found in the pneumococcus genome are predicted to be sugar transporters, with a high proportion of these being ATP-binding cassette (ABC) transporters. Bacterial ABC transporters play an important role in organism virulence and also have immunogenic potential (Garmory & Titball, 2004).
S. pneumoniae TIGR4 open reading frame SP1897 encodes a protein, designated RafE, that is predicted to be the substrate-binding component of an ATP-binding cassette (ABC) transport system (Rosenow et al., 1999). It shares 60.3% sequence identity (76.7% similarity) with MsmE from S. mutans, the substrate-binding domain of an ABC transport system responsible for the uptake of multiple sugars including raffinose, melibiose and isomaltotriose (Russell et al., 1992). In common with substrate-binding proteins from other Gram-positive bacteria (Gilson et al., 1988), MsmE contains a lipid-attachment site (conserved in RafE), which allows anchoring of the protein to the cell membrane by cleavage upstream of cysteine residue 23 and attachment of a fatty-acid lipid (Sutcliffe et al., 1993). It appears that sequence differences between RafE and MsmE result in different substrate specificities, with RafE only capable of raffinose transport (Rosenow et al., 1999). We present here preliminary crystallization and X-ray diffraction studies of a truncated form of RafE.
A polymerase chain reaction (PCR) product containing the coding region for a truncated form of RafE (residues 24-419) was cloned between the BamHI and HindIII sites of the pQE-10 vector (Qiagen) with an in-frame N-terminal His6 tag and linker (MRGSHHHHHHTDP). Transformation was carried out into Escherichia coli strain BL21 (DE3) and the cells were grown overnight on LB-agar plates containing 50 µg ml-1 ampicillin at 310 K. Single colonies were used to inoculate overnight cultures.
Cultures for induction (8 × 1 l) were each inoculated with 1 ml of a 10 ml 310 K overnight LB culture containing 50 µg ml-1 ampicillin and grown at 310 K. Isopropyl thio--D-galactoside (IPTG) was added to a final concentration of 1 mM at A600 = 0.6. After 16 h growth at 310 K, the cells were harvested by centrifugation at 3500g and 277 K for 15 min. Cells were resuspended in lysis buffer [50 mM Tris-HCl pH 8.0, 500 mM NaCl, 1× EDTA-free protease-inhibitor tablet (Roche) per 25 ml] and lysed by sonication (Status US200 with TT13 tip, 10 × 30 s bursts at 100% power). Cell debris was pelleted by centrifugation at 8000g and 277 K for 15 min and any residual cell debris was removed by a further centrifugation of the supernatant at 40 000g and 277 K for 20 min. Supernatant was loaded onto an Ni-NTA (Qiagen) column previously equilibrated with 50 mM Tris-HCl pH 8.0, 300 mM NaCl and washed with this buffer until A280 was constant. Protein was eluted with a gradient to 50 mM Tris-HCl pH 8.0, 300 mM NaCl, 500 mM imidazole. Eluted fractions containing RafE were pooled and concentrated at 2000g and 277 K to 60 mg ml-1 (Amicon, 10 kDa molecular-weight cutoff), calculated using a theoretical extinction coefficient of 80 790 M-1 cm-1 (Gasteiger et al., 2005). Gel filtration was performed using a 100 ml Superdex 75 (Amersham) column equilibrated with 10 mM Tris-HCl pH 8.0, 50 mM NaCl and a load volume of 1 ml. Retardation of the protein through the column was observed, possibly owing to interaction with the cross-linked agarose-dextran matrix, and this allowed selection of an active form of the protein. Eluted protein was judged to be over 95% pure by SDS-PAGE analysis. The protein was then concentrated to 20 mg ml-1 by centrifugation at 2000g and 277 K (Amicon, 10 kDa molecular-weight cutoff).
Sequence analysis of RafE showed 11 non-terminal methionine residues and a molecular weight of 46.7 kDa, making it a good candidate for phasing by selenomethionine labelling. Selenomethionine-labelled protein was prepared using methionine-biosynthesis inhibition (Van Duyne et al., 1993). A 10 ml 310 K overnight LB culture containing 50 µg ml-1 ampicillin and 25 µg ml-1 kanamycin was prepared and gently pelleted by centrifugation at 2000g and 300 K for 5 min. This pellet was resuspended in 10 ml M9 minimal medium pre-warmed to 310 K and used to inoculate selenomethionine growth media comprising M9 minimum medium plus sterile filtered MgSO4 (1 mM), glucose [0.4%(w/v)], thiamine [0.00005%(w/v)] and FeSO4 (15 µM). Cells were grown at 310 K to an A600 of 0.3, at which point L-selenomethionine (Acros Organics; 50 mg l-1), L-leucine (50 mg l-1), L-lysine (100 mg l-1), L-isoleucine (50 mg l-1), L-phenylalanine (100 mg l-1), L-threonine (100 mg l-1) and L-valine (50 mg l-1) were added, followed 15 min later by 1 mM IPTG. Cells were grown to A600 = 1.0 and then harvested by centrifugation at 3500g and 277 K for 15 min. Purification of selenomethionine-labelled RafE was carried out as previously described, with the addition of reducing agent at each stage. Lysis and Ni-NTA buffers were supplemented with 10 mM -mercaptoethanol. Following elution from the Ni-NTA column, 10 mM DTT was added to the protein and used in all subsequent buffers. The retardation on the Superdex-75 column previously described was also observed for selenomethonine-labelled RafE. Incorporation of selenomethionine was checked by MALDI-TOF mass spectroscopy and found to be 100%.
Crystallization trials were performed using the sitting-drop vapour-diffusion method at 295 K with a protein concentration of 20 mg ml-1 in 10 mM Tris-HCl pH 8.0, 50 mM NaCl. Initial screening was conducted using Hampton Research 24-well Cryschem Plates, a drop volume of 1.5 µl protein and 1.5 µl reservoir solution and a reservoir volume of 750 µl. Drops were mixed by aspiration. Screening was conducted using Hampton Research Crystal Screens 1 and 2 (Jancarik & Kim, 1991), Emerald Biosystems Wizard 1 and 2 and Cryo 1 and 2, Molecular Dimensions Structure Screen 1 and 2 and a wide range of in-house conditions.
Initial screening revealed single crystals in Crystal Screen 2 condition No. 14 and Structure Screen 2 condition No. 29. Both conditions are comprised of 2.0 M ammonium sulfate, 0.2 M sodium/potassium tartrate, 0.1 M sodium citrate pH 5.6. Crystals appeared after 3 d and continued growing for several months, but showed relatively poor diffraction, with a resolution limit of around 4.5 Å. Optimizations using Additive Screens 1, 2 and 3 (Hampton Research) with the original condition yielded crystals in 43 of the 72 conditions. These were all flash-cooled in liquid nitrogen using dry paraffin oil as a cryoprotectant (Riboldi-Tunnicliffe & Hilgenfeld, 1999). Owing to the large number of crystals, they were screened at the SRS Daresbury, beamline 14.2, using the Actor robotic system (Rigaku MSC). Divalent cations proved the best additives, in particular MgCl2 (10 mM), CaCl2 (10 mM), CoCl2 (10 mM), CuCl2 (10 mM) and CdCl2 (10 mM), with diffraction visible to 3.65 Å. Data were collected from a crystal grown in 2.0 M ammonium sulfate, 0.1 M Tris-HCl, 0.2 M sodium/potassium tartrate and CdCl2 (10 mM) at the SRS Daresbury, beamline 14.2, using a MAR CCD detector and a crystal oscillation of 1° per frame. A summary of the data-collection statistics is given in Table 1. The data were processed and scaled using the d*TREK package (Pflugrath, 1999) with systematic absences indicating a space group of either P6122 or P6522, with unit-cell parameters a = b = 145.10, c = 226.98 Å, = = 90.0, = 120.0°. The number of molecules in the asymmetric unit was also ambiguous at this stage, with either two (VM = 3.76 Å3 Da-1, 67.33% solvent content), three (VM = 2.51 Å3 Da-1, 50.99% solvent content) or four (VM = 1.88 Å3 Da-1, 34.66% solvent content) molecules per asymmetric unit.
Optimization of the initial crystallization condition discovered for the native protein yielded crystals that appeared identical to those previously obtained. Adjusting the conditions to 1.8 M ammonium sulfate, 0.1 M sodium citrate pH 5.1 and 0.2 M MgCl2 yielded the best-looking crystals (Fig. 1) and these were flash-cooled as previously described. An XAFS scan at the SRS Daresbury, beamline 14.2, showed a strong signal at the selenium edge and following analysis with CHOOCH (Evans & Pettifer, 2001; Fig. 2), diffraction data were collected at the peak wavelength of 0.9792 Å. Fig. 2 shows the importance of collecting an accurate fluorescence scan from a selenomethionine-labelled protein crystal, as collection at the theoretical selenium absorption edge of 0.9795 Å (12657.9 eV) would have missed the actual absorption edge of this crystal and resulted in very low anomalous signal. Data-collection statistics are shown in Table 1. These data were processed and scaled using d*TREK and 33 potential Se sites were found using SnB (Blessing & Smith, 1999; Smith et al., 1998; Turner et al., 1998; Weeks & Miller, 1999) with a clear bimodal distribution of correct and incorrect solutions. The top 14 of these sites with peak height greater than 6 were subjected to maximum-likelihood heavy-atom parameter refinement using SHARP (Bricogne et al., 2003) and an additional two sites were identified from subsequent residual map analysis. Solvent flattening was performed using SOLOMON (Abrahams & Leslie, 1996) and indicated an optimal solvent content of 69.8%, suggesting the presence of two molecules per asymmetric unit, and produced readily interpretable maps (Fig. 3) that confirm the space group as P6122. Maps generated in P6522 were uninterpretable.
| || Figure 1 |
Crystals of selenomethionine-labelled RafE. The dimensions of the largest crystal are approximately 400 × 400 × 250 µm.
| || Figure 2 |
Scattering plot obtained from selenomethionine-labelled crystals. Figure produced using CHOOCH (Evans & Pettifer, 2001).
| || Figure 3 |
Experimental electron-density maps obtained from selenomethionine phasing contoured at 1.5. Figure produced using Coot (Emsley & Cowtan, 2004). Located Se-atom positions are indicated by grey spheres.
Both native and selenomethionine-labelled RafE from S. pneumoniae have been crystallized in space group P6122 with two molecules in the asymmetric unit. Phasing using selenomethionine SAD data has been successful and has produced good-quality electron-density maps, although it is clear that in the asymmetric unit one molecule is well ordered while the other shows significant disorder in a number of regions. Of the 16 selenium sites found, 11 are from the well ordered molecule and show clear density. Model building is currently in progress and it appears that RafE shares the same periplasmic binding protein fold as seen in other ABC substrate-binding protein structures (Murzin et al., 1995).
We would like to thank the beamline staff at station 14.2, SRS for help and support during data collection. This work was made possible by a studentship awarded to NGP by the Biotechnology and Biological Sciences Research Council (BBSRC).
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