|Home | About | Journals | Submit | Contact Us | Français|
Lanthanoid ions exhibit extremely large anomalous X-ray scattering at their L III absorption edge. They are thus well suited for anomalous diffraction experiments. A novel class of lanthanoid complexes has been developed that combines the physical properties of lanthanoid atoms with functional chemical groups that allow non-covalent binding to proteins. Two structures of large multimeric proteins have already been determined by using such complexes. Here the use of the luminescent europium tris-dipicolinate complex [Eu(DPA)3]3− to solve the low-resolution structure of a 444 kDa homododecameric aminopeptidase, called PhTET1-12s from the archaea Pyrococcus horikoshii, is reported. Surprisingly, considering the low resolution of the data, the experimental electron density map is very well defined. Experimental phases obtained by using the lanthanoid complex lead to maps displaying particular structural features usually observed in higher-resolution maps. Such complexes open a new way for solving the structure of large molecular assemblies, even with low-resolution data.
Even though most of the newly deposited structures in the Protein Data Bank (PDB) were solved by molecular replacement, experimental phasing remains essential for determining three-dimensional protein structures if only for solving structures with new folds or which significantly differ from any known model structure. Over the last ten years, methods based on anomalous scattering, namely the single-wavelength anomalous diffraction (SAD) and multiple-wavelength anomalous diffraction (MAD) methods, have replaced the traditional methods based on isomorphous replacement, thus becoming the methods of choice for solving de novo protein structures. Consequently, the preparation of effective heavy-atom derivatives displaying anomalous scattering has become a key point for de novo crystal structure determination. With the incorporation of selenium through the substitution of methionine residues by seleno-methionine (Hendrickson et al., 1990 ; Doublie, 1997 ), and with the developments at third-generation synchrotron radiation sources, which allow weak anomalous signals from intrinsic scatterers to be used, the time-consuming preparation of heavy-atom derivatives has been facilitated.
However, the use of such procedures is not always possible, which revives the problem of incorporating effective anomalous scatterers into protein crystals. Therefore, we proposed to use lanthanoid complexes for preparing lanthanoid derivative crystals (Girard et al., 2002 ). Lanthanoid ions, Ln3+, are well suited to anomalous diffraction experiments since they all exhibit a strong white line in their L III absorption edge leading to extremely large anomalous contributions of almost 30 e− for both f′ and f′′.
A way to assess the phasing power of lanthanides is to compare them with the most frequently used anomalous scatterer, i.e. selenium from seleno-methionine. For this purpose the Bijvoet ratio can be considered. We have shown (Girard, Stelter et al., 2003 ) that the Bijvoet ratio can be expressed as
where is the number of atoms of the protein of mean scattering factor , and are the site occupancy and the imaginary part of the atomic scattering factor of the anomalous scatterer , respectively. This formula clearly shows that, assuming fixed site occupancies, identical Bijvoet ratios are obtained for a protein that is four times larger when is doubled for each anomalous scatterer. Assuming that the diffraction data are collected at the respective absorption edge, values are about 10 and 30 e− for selenium and lanthanoid, respectively. This means that one fully occupied lanthanoid atom will allow a protein that is nine times larger, compared with a fully occupied Se atom, to be phased.
Hence, lanthanoids are good candidates for macromolecular structure determination based on the use of the anomalous signal. Lanthanoid ions were used in early MAD studies on calcium-binding proteins (Kahn et al., 1985 ; Weis et al., 1991 ) as they can substitute for Ca2+. Nagem et al. (2001 ) proposed to incorporate lanthanoid salts through the quick cryo-soak method, but soaking crystals in solutions containing lanthanoid salts often damages the crystals owing to the preferred nine-based coordination of lanthanoid ions. To overcome this problem, Purdy et al. (2002 ) proposed to use a covalent linkage between a lanthanoid complex featuring a saturated coordination sphere and the protein of interest through a thio-reactive functionality, and Silvaggi et al. (2007 ) proposed to use a double lanthanoid-binding tag.
Girard et al. (2002 ) proposed to use gadolinium complexes initially used as contrast agents for magnetic resonant imaging to incorporate lanthanoid ions into protein crystals. Seven different gadolinium complexes were studied (Girard, Stelter et al., 2003 ). These complexes are made of a ligand that surrounds the lanthanoid ions as a cage, thus providing the majority of the coordination sphere of the ion. More recently, we have proposed to use complexes based on dipicolinate (DPA = pyridine-2,6-dicarboxylate) ligands, namely the lanthanoid tris-dipicolinate complex ions [Ln(DPA)3]3−, the Eu and Tb complexes being luminescent (D’Aléo et al., 2007 ; Pompidor et al., 2008 ). As previously mentioned, lanthanoid salts often damage protein crystals even at low concentration. The great advantage of using lanthanoid complexes comes from the fact that the interaction of the lanthanoid ions with the protein occurs through the ligand forming the complexes rather than direct interaction. The binding mode of the various used complexes to the protein turned out to depend on the nature of the ligand (Girard, Anelli et al., 2003 ). These complexes can be introduced in protein crystals either by co-crystallization or soaking and can be used at rather high concentration (50 to 100 mM).
The technique of introducing lanthanoid ions into protein crystals by using lanthanoid complexes1 was successfully used to solve the structure of several proteins (Chaudhuri et al., 2003 ; de Bono et al., 2005 ; Hermoso et al., 2005 ; Jeudy et al., 2005 ; Márquez et al., 2006 ; Gras et al., 2007 ; Delfosse et al., 2009 ; Molina et al., 2009 ; Arnoux et al., 2009 ; Pérez-Dorado, González et al., 2010 ; Pérez-Dorado, Sanles et al., 2010 ).
The lanthanoid complexes have also been used to solve structures of large macromolecular assemblies. The structure of a chimeric ornithine carbamoyl transferase, OTCase3630, a dodecamer of 450 kDa, was solved by using the SAD method (Girard, Stelter et al., 2003 ). More recently, the structure of the Pyrococcus abyssi Pab87 protein, an archaeal member of a new self-compartmentalizing protease family forming a cubic-shaped octamer of 400 kDa, was determined at 2.2 Å resolution by the SAD method (Delfosse et al., 2009 ).
Here, we report the use of the tris-dipicolinate complex to obtain experimental phases at low resolution on a large homo-dodecameric enzyme, PhTET1-12s, which is a tetrahedral aminopeptidase belonging to a new family of self-compartmentalized large protease complexes (Franzetti et al., 2002 ). The TET peptidase was initially isolated from Haloarcula marismortui (Franzetti et al., 2002 ). In the archae Pyrococcus horikoshii, three different open reading frames coding for TET-homologous proteins were identified. These were named PhTET1, 2 and 3. Their three-dimensional structures were determined (Franzetti et al., 2002 ; Russo & Baumann, 2004 ; Borissenko & Groll, 2005 ; Schoehn et al., 2006 ; Durá et al., 2009 ). It has been shown (Schoehn et al., 2006 ) that PhTET1 assembles as a tetrahedral dodecameric particle (called PhTET1-12s for the 444 kDa assembly made up of 12 subunits) or as an octahedral tetracosameric edifice (called PhTET1-24s for the 888 kDa assembly made up of 24 subunits).
Since the TET particles are highly symmetrical molecular edifices formed by a single type of subunit, they provide an excellent model for probing the phasing capacity of different lanthanoid complexes. Moreover, the currently available TET crystallographic structures do not permit detailed analyses of the particles interior. The polypeptide trafficking and the processing mechanisms by the TET particles remain therefore unclear. In this paper we show that low-resolution experimental phase obtained with tris-dipicolinate complex can provide novel structural information on the PhTET1-12s complex.
The expression of TET1-12s from P. horikoshii in Escherichia coli, its purification and initial crystallization assays will be described elsewhere (Dura et al., 2010 ). Na3[Eu(DPA)3].6H2O complex where DPA stands for pyridine-2,6-dicarboxylate (e.g. dipicolinate) was prepared using the procedure described by Tancrez et al. (2005 ).
Crystallization was performed by vapour diffusion using the hanging-drop method at 293 K. Native PhTET1-12s crystals (~200 µm × 140 µm × 20 µm) were grown within three weeks by mixing 1.5 µl of 6.2 mg ml−1 protein solution and 1.5 µl of 20–22% PEG 3350 (or 20% PEG 2000 MME), 100 mM Tris-HCl buffer at pH 7.5 and 200 mM trimethylamine N-oxide reservoir solution. PhTET1-12s derivative crystals (~150 µm × 150 µm × 30 µm) were obtained within three weeks by cocrystallization with [Eu(DPA)3]3− by mixing 1.5 µl of 6.2 mg ml−1 protein solution, 1.5 µl of 220 mM Na3[Eu(DPA)3].6H2O solution and 1.5 µl of reservoir solution containing 23–24% PEG 3350 (or 23–26% PEG 2000 MME).
Prior to data collection, derivative crystals were cryo-cooled in liquid nitrogen using mother liquor containing 20% ethylene glycol as cryo-protectant.
SAD data were collected on the FIP-BM30A beamline at the ESRF. Based on a fluorescence scan, the wavelength was chosen at the L III europium absorption edge, and was set to 1.766 Å, which corresponds to the maximum value of f′′ (~28 e−). Diffraction data were integrated using the program XDS (Kabsch, 2010a ,b ) and the integrated intensities were scaled and merged using the CCP4 programs SCALA and TRUNCATE (Collaborative Computational Project, Number 4, 1994 ). A summary of the processing statistics is given in Table 1 .
As described in §2, we used crystallization conditions that led to a new high-resolution form of PhTET1-12s in space group P21 with an entire dodecamer in the asymmetric unit (Dura et al., 2010 ). Surprisingly, the addition of the tris-dipicolinate complex led to the initial F4132 crystal form diffracting at low resolution, that was used for the initial structure determination of PhTET1-12s at 3.09 Å resolution (Porciero et al., 2005 ; Schoehn et al., 2006 ).
As shown in Table 1 , the high value of R ano clearly indicated the presence of tris-dipicolinate europium complex binding sites, which was then confirmed by the anomalous Patterson map. Despite the low resolution of the data, we attempted de novo phasing of the structure of PhTET1-12s. Using the program SHELXD (Sheldrick, 2008 ), we were able to locate one Eu site per TET-monomer. Heavy-atom refinement and initial phasing were performed using the program SHARP (La Fortelle & Bricogne, 1997 ). Phases from SHARP were improved by density modification using the CCP4 program DM (Cowtan & Main, 1996 ) assuming a solvent content of 50%.
Despite the low resolution, the experimental phases were accurate since the figure of merit after SHARP and DM are 0.369 and 0.731, respectively. The resulting experimental electron density map was of good quality (Fig. 1a ) since it allowed the polypeptide chain to be traced, as shown in Fig. 2(a) . The overall shape of the PhTET1-12 subunit particle could be easily recognized with, on one side of the particle, the large channel (Fig. 1b ) assumed to be the entrance for the peptide substrate and, on the other side, the small channel (Fig. 1c ) assumed to be the exit pathway for the reaction products, which are individual amino acids.
We performed SIRAS (single isomorphous replacement with anomalous scattering) phasing using the 3.09 Å resolution native data set from which the structure of PhTET1-12s (PDB code 2cf4) was solved by molecular replacement (Rossmann, 1990 ). As for the SAD phasing, the SIRAS experimental phases were accurate since the figure of merit after SHARP and DM were 0.211 and 0.785, respectively. Despite the introduction of the tris-dipicolinate europium complex, the isomorphism between the native and derivative crystals was preserved. The resulting SIRAS electron density map was of high quality, as shown in Fig. 2(b) .
We have shown that, using [Eu(DPA)3]3−, the high-phasing-power heavy-atom derivative of PhTET1-12s may be obtained by co-crystallization. Highly accurate experimental phases were obtained, even at the low resolution of this work (4.0 Å). The presence of the [Eu(DPA)3]3− complex modified the crystal space group: from crystallization conditions that led to the monoclinic crystal form diffracting at high resolution, the introduction of [Eu(DPA)3]3− induced the formation of cubic crystals. Pompidor et al. (2010 ) showed that the interaction between the protein and the [Ln(DPA)3]3− complex occurs through hydrogen bonds between the O atom of the carboxylate groups of the DPA ligands and hydrogen-bond donor residues, and through hydrophobic π-stacking interaction between DPA rings and aromatic residues. In some cases this specific binding mode improves the protein–protein interaction involved in crystal packing leading to supramolecular interactions. In the present structure it seems that it is not the case. Even if the low resolution of the data limits the modelling of the DPA ligand, the Eu3+ ion is located between two monomers on the large channel side of the particle, as shown in Fig. 2(c) . These two monomers are supposed to be the minimal building block of the whole particle. Since the [Eu(DPA)3]3− complex is bound within this building block, it did not directly influence the molecular packing as would be the case if bridging two building blocks. A possible explanation for the space group change is that binding of the tris-dipicolinate europium complex induces a small conformational change in the PhTET1-12s protomer, leading to the growth of the low-resolution crystal form.
The tris-dipicolinate europium complex binding site is located in the vicinity of a loop, which is assumed to be a key player in the addressing of the substrate toward the catalytic chambers of the TET particle (Durá et al., 2009 ). To obtain new insights into this important functional zone, we therefore plan to attempt to increase the resolution of the experimental data either by soaking PhTET1 crystals in solutions containing [Eu(DPA)3]3− or by preparing [Eu(DPA)3]3− derivative crystals of PhTET2 or PhTET3, in order to obtain more precise experimental (i.e. model-bias free) information.
As mentioned, the binding of the lanthanoid complexes to the protein depends on their ligand, the non-covalent interaction being for example hydrophobic (for the complex Gd-HPDO3A; Girard, Stelter et al., 2003 ) or through hydrogen bonding between arginine/lysine residues and the dipicolinate complex (Pompidor et al., 2010 ). Thus, the probability of occurrence of the appropriate binding sites in the protein increases with the protein size. Combined with the strong anomalous signal of the lanthanoid ions, these complexes are thus efficient tools for solving the structure of large macromolecular assemblies, irrespective of their size.
This work was supported by the French National Research Agency (ANR Project MacroTET; BLAN07-3_204002).
1The different lanthanoid complexes can be purchased from NatX-ray (http://www.natx-ray.com/home.html).