Structure of the inhibitor complex of old yellow enzyme from Trypanosoma cruzi
aDepartment of Applied Chemistry, Graduate School of Engineering, Osaka University, Yamada-Oka 2-1, Suita, Osaka 565-0871, Japan, bNational Institute of Health Sciences (NIHS), Tokyo 158-8501, Japan, cMARUWA Foods and Biosciences, Tsutsui-cho 170-1, Yamatokoriyama, Nara 639-1123, Japan, and dDepartment of Molecular Behavior Biology, Osaka Bioscience Institute, Osaka 565-0874, Japan
*Correspondence e-mail: firstname.lastname@example.org
Old yellow enzyme (OYE) is an NADPH oxidoreductase which contains flavin mononucleotide as prosthetic group. The X-ray structures of OYE from Trypanosoma cruzi (TcOYE) which produces prostaglandin (PG) F2α from PGH2 have been determined in the presence or absence of menadione. The binding motif of menadione, known as one of the inhibitors for TcOYE, should accelerate the structure-based development of novel anti-chagasic drugs that inhibit PGF2α production specifically.
Prostaglandin (PG) F2α synthase (PGFS) is the enzyme which produces PGF2α from the PGH2, and was first isolated from mammals (Watanabe et al., 1985). Mammalian PGFSs belong to aldo-ketoreductases (Bohren et al., 1989; Bruce et al., 1994), which are NAD(P)(H)-dependant oxidoreductase. In mammals, PGF2α is a potent mediator of various physiological processes (Narumiya et al., 1999; Glew, 1992; Samuelsson, 1979) including vasculartone, constriction of uterine muscle (Bygdeman et al., 1970) and pulmonary arteries (Oliw et al., 1983; Mathe et al., 1977), and induction of luteolysis during the estrous cycle and prior to parturition (Horton & Poyser, 1976; McCracken et al., 1972). During pathological processes in mammals, PGF2α overproduction causes ovarian dysfunction and miscarriage (Dubois et al., 1998; Mutayoba et al., 1989; Davies et al., 1984).
PGF2α is produced not only in mammals but also in parasitic protozoa which causes serious infections, such as Plasmodium falciparum (Kubata et al., 1998), Trypanosoma brucei (Kubata et al., 2000; Okano et al., 2002; Kilunga et al., 2005) and Leishmania major (Kabututu et al., 2002, 2003). Owing to their identification, pathological relationships of parasitic PGFSs with human disease have begun to emerge. For example, it is thought that PGFS from Trypanosoma brucei (TbPGFS) plays a role in pathogenesis trypanosomiasis because African trypanosomiasis is characterized by miscarriage owing to PGF2α overproduction correlated with parasitemia peaks (Mutayoba et al., 1989). Therefore, the study of parasitic PGFS is quite significant because it can lead to investigation of the pathological roles and development of the inhibitor of PGFS for remedies.
Chagas disease, caused by Trypanosoma cruzi, affects more than 20 million people and poses a major public health and economic problem in South America (World Health Organization, 1990). This situation has been worsened by the lack of effective vaccines and undesirable side effects of anti-chagasic drugs, such as nifurtimox and benznidazole (Aldunate & Morello, 1993; Henderson et al., 1988; Docampo & Moreno, 1986; Docampo, 1990), in addition to the emergence of parasite resistance to these drugs. Therefore, the development of a new chemotherapeutic treatment is an urgent need.
PGFS from T. cruzi was identified by Kubata et al. and it was found that this enzyme belonged to old yellow enzyme (OYE) (Kubata et al., 2002). OYE was originally isolated from brewers' bottom yeast in the 1930s, and the first protein requiring a vitamin B2-derived molecule, flavin mononucleotide (FMN), of its catalysis (Warburg, 1933; Schopfer & Massey, 1991). The previously detected OYE families from bacteria (Warburg, 1933; Matthews & Massey, 1969), yeast (Schaller & Weiler, 1997) and plants (French et al., 1996; Blehert et al., 1999) are able to reduce a variety of compounds, such as unsaturated aldehydes and ketones (French & Bruce, 1994; Vaz et al., 1995), nitro-esters (French et al., 1996; Snape et al., 1997; Blehert et al., 1999; Meah & Massey, 2000) and nitro-aromatic substrates (French et al., 1998; Pak et al., 2000; Williams et al., 2004).
OYE from T. cruzi (TcOYE) catalyzes prostaglandin F2α synthesis (Fig. 1) as well as the reduction of many kinds of trypanocidal drugs, such as naphtoquinone and nitroheterocyclic compounds (Kubata et al., 2002). By electron spin resonance it was found that these compounds can undergo either one- or two-electron reduction. Naphtoquinone, such as menadione (Km = 0.82 µM) or β-lapachone (Km = 0.17 µM), is reduced by one-electron reduction, generating semiquinone radicals which cause the cell death in susceptible parasites, while nitroheterocyclic compounds, such as 4-nitroquinoline-N-oxide (Km = 9.5 µM) or nifurtimox (Km = 19.0 µM), are reduced by two-electron reduction (Kubata et al., 2002). Therefore, three-dimensional information of the structure in complex with the quinine compounds is valuable for the design of novel anti-chagasic drugs by which semiquinone radicals are more efficiently generated in T. cruzi.
Here we report the first X-ray structures of TcOYE which produces PGF2α from PGH2 in the presence or absence of menadione. The structural analysis of TcOYE/FMN/menadione ternary complex has provided the binding motif of menadione at the active site. These structures are useful for further drug design for Chagas disease.
Chemicals were obtained from Sigma-Ardrich at the highest available purity. TcOYE was overexpressed in E. coli and purified, and TcOYE/FMN binary complex was crystallized according to previously reported methods (Kubata et al., 2002; Sugiyama et al., 2007). These crystals were flash-cooled in liquid nitrogen with cryo-protectant solution containing 3% (v/v) 2-methyl-2,4-pentanediol. The X-ray diffraction data were obtained up to 1.70 Å resolution at SPring-8 beamline BL41XU. The diffraction data were processed and scaled using the program HKL2000 (Otwinowski & Minor, 1997).
2.2. Structure determination and refinement
The structure of TcOYE was determined by molecular replacement with the program AMoRe (Navaza, 2001) using the structure of morphinone reductase from Pseudomonas putida (Protein Data Bank code 1gwj ) (Barna et al., 2002) as a search model. Crystallographic refinement was carried out with the program CNS (Brünger et al., 1998). The refinement procedure included simulated annealing, positional refinement, restrained temperature factor refinement, and maximum-likelihood algorithms as provided by the CNS program. Electron density maps based on the coefficients of 2Fo − Fc and Fo − Fc were used to build the atomic models in Coot (Emsley & Cowtan, 2004). Water molecules were inserted manually and then checked by inspecting the Fo − Fc map. FMN (cofactor) and menadione (ligand) were refined using atomic parameters extracted from the HIC-UP server (Kleywegt & Jones, 1998), and could be inserted into the clearly defined electron density model after some cycles of refinement.
In order to prepare the complex crystals with menadione, the crystals of the TcOYE/FMN complex were soaked in a menadione solution for 16 h and then the crystals were flash frozen in liquid nitrogen. The X-ray diffraction data were obtained up to 2.5 Å resolution by using Ultrax18 (Rigaku). Data collection, structure determination and refinement were carried out by the same methods as described above.
The structure of TcOYE/FMN binary complex was determined by molecular replacement methods using that of morphinone reductase (Barna et al., 2002) as the searching model and refined at 1.7 Å resolution with final Rcryst/Rfree values of 18.5%/23.2%. Our crystallographic properties and refinement statistics of the structure are presented in Table 1.
‡Rcryst = Σ||Fo| − |Fc||/Σ|Fo|, calculated from 90% of the data, which were used during the course of the refinement.
§Rfree = Σ||Fo| − |Fc||/Σ|Fo|, calculated from 10% of the data, which were obtained during the course of the refinement.
TcOYE, like other members of the OYE family, folds into an (α/β)8 barrel in which the cylindrical core composed of eight parallel β-strands (β1–β8) is surrounded by eight α-helices (α1–α8). In addition, an N-terminal β-hairpin (S1 and S2) closes the bottom of the barrel and two extra helices (H1 and H2) lie in the loops connecting β4 to α4 and β8 to α8, respectively (Fig. 2). The loop regions from 105 to 165 (Loop 1) and 351 to 379 (Loop 2) exhibit the relatively higher B-factors of 21.3 and 18.8 Å2, respectively, while the overall B-factor of TcOYE without those two loop ranges was calculated to be 13.1 Å2. This difference in the B-factor shows the flexibility of these two loops.
FMN is tightly bound at the C-terminal ends of the eight β-strands in the barrel and exhibits quite low B-factors (Fig. 3). Most amino acid residues which bind to the riboflavin moiety of FMN are highly conserved among the different known OYE structures, except Ala61. Ala61 in TcOYE was conserved as alanine or glycine among the known OYE structures; however, the amide nitrogen atom of the corresponding amino acid interacts with O4 of FMN. On the other hand, three residues bound to the phosphate O atoms in FMN are not conserved: the side chain of Asn313 and the main chains of Leu314 and Lys338 interact with the phosphate O atoms through water molecules.
In order to develop more effective inhibitors we have solved the structure of TcOYE/FMN/menadione ternary complex at 2.5 Å resolution (Table 1). The whole structure of TcOYE does not change even upon binding of menadione. The binding motif of menadione is defined in the difference electron density maps even at low occupancy (Fig. 4). The cause of its low affinity (Km = 0.82 µM) is assumed to be because the ligand is stabilized by only a π–π interaction with the isoalloxazien ring of FMN. To increase the affinity of menadione, interactions with His195, Asn198 or Tyr 364 should be designed in the future.
We have solved the structures of TcOYE in the presence or absence of menadione. The binding motif of the inhibitor at the active site of TcOYE has been elucidated from TcOYE/FMN/menadione ternary complex. Future work is in progress to obtain the structure in complex with other inhibitors to elucidate the reaction mechanism of TcOYE in detail, which can be expected to lead to the development of heroic anti-chagasic drugs.
The authors express their appreciation to Professor B. K. Kubata, Biosciences Eastern and Central Africa, and Dr Z. Kabututu, Osaka Bioscience Institute, for their early support of the protein expression. The authors are grateful to M. Yoshimura, M. Yamashita, E. Yamashita and A. Nakagawa at SPring-8 beamlines 12B2, 40B2 and 44XU for fundamental data collection, and to N. Shimizu and K. Hasegawa for their kind support during data collection at SPring-8 beamline 41XU. This work was supported by Grants-in-Aid for Scientific Research (Nos. 16017260 and 18350086) from the Ministry of Education, Culture, Sports, Science and Technology of Japan and the PRESTO project, Japan Science and Technology Agency, the National Project on Protein Structural and Functional Analyses, Japan (to TI), and the Center of Excellence (21COE) program `Creation of Integrated EcoChemistry of Osaka University' (to KT), and was partly supported by the Applied Research Pilot Project for the Industrial Use of Space promoted by JAXA and Japan Space Utilization Promotion Center (JSUP) and a grant from Japan Foundation for Applied Enzymology and Osaka City (to YU)
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