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Broad Specificity of Mammalian Adenylyl Cyclase for Interaction with 2',3'-Substituted Purine- and Pyrimidine Nucleotide Inhibitors

Department of Biochemistry, University of Texas Southwestern Medical Center at Dallas, Dallas, Texas (T.-C.M., S.R.S.); Department of Pharmacology and Toxicology, the University of Kansas, Lawrence, Kansas (A.G., R.S.); Department of Molecular Biosciences, the University of Kansas, Lawrence, Kansas (S.S., M.R.); and Department of Pharmacology and Toxicology, University of Regensburg, Regensburg, Germany (R.S.)

Received May 8, 2006; accepted June 8, 2006

	Abstract

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Membrane adenylyl cyclases (mACs) play an important role in signal transduction and are therefore potential drug targets. Earlier, we identified 2',3'-O-(N-methylanthraniloyl) (MANT)-substituted purine nucleotides as a novel class of highly potent competitive mAC inhibitors (K_i values in the 10 nM range). MANT nucleotides discriminate among various mAC isoforms through differential interactions with a binding pocket localized at the interface between the C1 and C2 domains of mAC. In this study, we examine the structure/activity relationships for 2',3'-substituted nucleotides and compare the crystal structures of mAC catalytic domains (VC1:IIC2) bound to MANT-GTP, MANT-ATP, and 2',3'-(2,4,6-trinitrophenyl) (TNP)-ATP. TNP-substituted purine and pyrimidine nucleotides inhibited VC1:IIC2 with moderately high potency (K_i values in the 100 nM range). Elongation of the linker between the ribosyl group and the MANT group and substitution of N-adenine atoms with MANT reduces inhibitory potency. Crystal structures show that MANT-GTP, MANT-ATP, and TNP-ATP reside in the same binding pocket in the VC1:IIC2 protein complex, but there are substantial differences in interactions of base, fluorophore, and polyphosphate chain of the inhibitors with mAC. Fluorescence emission and resonance transfer spectra also reflect differences in the interaction between MANT-ATP and VC1:IIC2 relative to MANT-GTP. Our data are indicative of a three-site mAC pharmacophore; the 2',3'-O-ribosyl substituent and the polyphosphate chain have the largest impact on inhibitor affinity and the nucleotide base has the least. The mAC binding site exhibits broad specificity, accommodating various bases and fluorescent groups at the 2',3'-O-ribosyl position. These data should greatly facilitate the rational design of potent, isoform-selective mAC inhibitors.

We have discovered that the fluorescent 2'(3')-O-(N-methylanthraniloyl) (MANT) derivative of GTP (MANT-GTP) is a highly potent competitive inhibitor of several mAC isoforms as well as of the soluble VC1:IIC2 complex (Gille and Seifert, 2003; Gille et al., 2004). This finding was surprising in view of the high selectivity of mAC toward ATP in preference to GTP as a substrate (Sunahara et al., 1998; Gille et al., 2004). The crystal structure of the VC1:IIC2 complex with MANT-GTP revealed that the MANT nucleotide is bound to the catalytic site in reverse orientation with respect to ATP analogs that are not derivatized with bulky substituents at the 2'(3') position. In the reverse orientation, the guanine moiety in the purine binding site is accommodated by a pattern of hydrogen bonds analogous to those formed with adenine (Mou et al., 2005). The reverse orientation of MANT-GTP in the catalytic site is a consequence of the intercalation of the MANT moiety into a hydrophobic pocket at the interface between the C1 and C2 domains. Other MANT nucleotides, such as MANT-ATP, also inhibit G_s/FSK-activated VC1:IIC2 with K_i values in the 10 to 100 nM range (Gille et al., 2004). Thus, the catalytic site of mAC exhibits a much lower base specificity toward 2'(3')-MANT nucleotides than was previously observed for other ATP analogs. The relaxation of specificity may arise from enlargement of the inhibitor-binding pocket as a result of the insertion of the MANT group into the interdomain site.

The forgoing findings prompted us to study in more detail the inhibition of VC1:IIC2 by 2',3'-substituted purine and pyrimidine nucleotides. In particular, we examined MANT-EDA-ATP, which possesses a longer linker between the ribosyl moiety and the fluorophore, and three analogs (6-MANT-ATP, MABA-ATP, and MAHA-ATP) in which the fluorophore is attached to N6 and N8, respectively, of adenine through various linkers. We also examined 2',3'-substituted TNP nucleotides, which are widely used for studying conformational changes in proteins (Hiratsuka, 2003). Fluorescence analysis suggested that MANT-GTP and MANT-ATP bind to VC1:IIC2 in slightly different ways, calling for more detailed analysis by X-ray crystallography. In this study, we show that MANT-GTP, MANT-ATP, and TNP-ATP bind to a common site in mAC, but they do so in different ways, as corroborated by fluorescence spectroscopy. These data support the concept that the catalytic site of mAC, if structurally perturbed at the domain interface, shows broad specificity for active site-directed inhibitors. It may be inferred from our data that potent mAC inhibitors can be designed with considerable latitude with respect to the composition of the moieties that fill distinct subsites within the catalytic pocket of the enzyme.

	Materials and Methods

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Materials. Recombinant adenylyl cyclase cytosolic C1a domain from canine type V (VC1), C2a domain from rat type II (IIC2), and bovine G_s were purified and stored as described previously (Tesmer et al., 2002). G_s was activated by incubation with 10 µM GTPS and 2 mM MgCl₂ at 30°C for 1 h, and the resulting G_s · GTPS complex was digested by trypsin. Free GTPS and inactivated G_s were removed by passing the sample through nickel-nitrilotriacetic acid resin. All MANT nucleotides, TNP-GDP, TNP-GTP, TNP-CTP, and TNP-UTP were obtained from Jena Bioscience (Jena, Germany). TNP-AMP, TNP-ADP, and TNP-ATP were obtained from Invitrogen (Eugene, OR). GTPS was from Roche (Indianapolis, IN). FSK and MP-FSK were obtained from Calbiochem (La Jolla, CA). Sources of other materials are described elsewhere (Gille and Seifert, 2003; Gille et al., 2004; Mou et al., 2005).

AC Activity Assays. AC activity was determined essentially as described previously (Mou et al., 2005). In brief, reaction mixtures contained 40 µM ATP/Mn²⁺, 10 mM MnCl₂, and MANT nucleotides or TNP nucleotides at concentrations from 1 nM to 1 mM as appropriate to obtain saturated inhibition curves. In addition, assay tubes contained VC1 (8 nM) and IIC2 (40 nM). For experiments with G_s ·GTPS, tubes contained VC1 (3 nM), IIC2 (15 nM), and G_s ·GTPS (51 nM). Reactions were conducted in the presence of 100 µM FSK. After a 2-min preincubation at 30°C, reactions were initiated by adding 20 µl of reaction mixture containing (final) 1.0 µCi/tube [-³²P]ATP, 0.1 mM cAMP, and 100 mM KCl in 25 mM Na⁺HEPES, pH 7.4. It should be noted that AC assays were conducted in the absence of an NTP-regenerating system to allow for the analysis of 2',3'-substituted NDPs and NMPs that would otherwise be phosphorylated to the corresponding NTPs by the regenerating system (Gille et al., 2004). Reactions were conducted for 10 to 20 min at 30°C and were terminated by the addition of 20 µl of 2.2 N HCl. Denatured protein was sedimented by a 1-min centrifugation at 25°C and 15,000g. Sixty-five microliters of the supernatant fluid were applied onto disposable columns filled with 1.3 g of type WN-6 neutral, activity grade Super I alumina (Sigma-Aldrich, St. Louis, MO). [³²P]cAMP was separated from [-³²P]ATP by elution of [³²P]cAMP with 4 ml of 0.1 M ammonium acetate, pH 7.0. Recovery of [³²P]cAMP was 80% as assessed with [³H]cAMP as standard. [³²P]cAMP was determined by erenkov radiation or liquid scintillation counting using Ecolume scintillation cocktail (Fisher, Pittsburgh, PA). Competition isotherms were analyzed by nonlinear regression using the Prism 4.0 software (GraphPad, San Diego, CA).

Fluorescence Spectroscopy and Data Analysis. All experiments were conducted using a Cary Eclipse fluorescence spectrophotometer equipped with a Peltier-thermostated multicell holder at 25°C (Varian, Walnut Creek, CA). Measurements were performed in a quartz fluorescence microcuvette (Hellma, Plainview, NY). The final assay volume was 150 µl. Reaction mixtures contained a buffer consisting of 100 mM KCl, 10 mM MnCl₂, and 25 mM Na⁺HEPES, pH 7.4. Steady-state emission spectra were recorded at low speed with _ex = 350 nm (_em = 370-500 nm) and _ex = 280 nm (_em = 300-500 nm) with 1 µM MANT-GTP or 1 µM MANT-ATP in the absence and presence of 5 µM VC1 plus 25 µM IIC2 without and with 100 µM MP-FSK. Fluorescence recordings were analyzed with the spectrum package of the Cary Eclipse software (Varian, Walnut Creek, CA). Baseline fluorescence (buffer alone) was subtracted. Figure 1 shows superimposed original fluorescence recordings. Similar results were obtained in four independent experiments using two different batches of VC1 and IIC2.

View larger version (35K): [in this window] [in a new window]   Fig. 1. Fluorescence emission spectra of MANT-GTP and MANT-ATP in the absence and presence of VC1:IIC2 and MP-FSK. Fluorescence measurements were conducted as described under Materials and Methods. A and B, measurements with MANT-GTP; C and D, measurements with MANT-ATP. Spectra were recorded at ex = 280 nm (em = 300-500 nm) in A and C and at ex = 350 (em = 300-500 nm) in B and D. Cuvettes containing VC1 (5 µM) and IIC2 (25 µM) in the presence of MP-FSK (100 µM) were equilibrated for 10 min at 25°C before recording spectra. MANT-GTP and MANT-ATP were used at a concentration of 1 µM each. Representative fluorescence emission spectra are shown for MANT-GTP/MANT-ATP alone (blue lines) and VC1:IIC2 (C1/C2) only (black dashed lines), MANT-GTP/MANT-ATP in the presence of VC1:IIC2 (green lines) and MANT-GTP/MANT-ATP in the presence of both VC1:IIC2 and MPFSK (red lines). Fluorescence intensities are shown in arbitrary units (a.u.). The black arrows in B and D indicate the emission maxima for MANT-GTP/MANT-ATP in the absence of VC1:IIC2 and in the presence of VC1:IIC2 plus MP-FSK. Fluorescence tracings are representative for five independent experiments with different protein batches.

Diffraction data sets were collected by the oscillation method at the Advanced Light Source (ALS) 8.2.1 beamline at Berkeley, CA with an incident beam wavelength of 1.0781Å, and the images were processed with the HKL2000 package (Otwinowski and Minor, 1997). As a result of anisotropy, data with l index >20 for crystals of the TNP-ATP ·Mn²⁺ complex and l index >18 for crystals of the MANT-ATP ·Mn²⁺ complex were excluded from the data set. Crystals of the protein complex with MANT-ATP ·Mn²⁺ or TNP-ATP ·Mn²⁺ were nearly isomorphous with those of the VC1:IIC2 ·FSK: G_s ·GTPS complex (Tesmer et al., 1997). Coordinates of the latter complex with MANT-GTP (Protein Data Bank code 1TL7 [PDB] ) were used as the initial phasing model. The inhibitors and metal ions in the structures were located in a SIGMA-A weighted |Fo| -|Fc| difference omit map computed with phases from the refined model. Atomic positions and thermal parameters were refined by successive rounds of rigid body, simulated annealing, Powell minimization, and B factor refinement using the CNS 1.1 program suite (Brunger et al., 1998). The model was iteratively improved by manual refitting into weighted 2|Fo| -|Fc| maps using the computer graphics program O (Jones et al., 1991), and subsequent cycles of refinement using CNS. Coordinates for the TNP-ATP ·Mn²⁺ and MANT-ATP ·Mn²⁺ structures have been deposited in the Protein Data Bank with the codes 2GVD and 2GVZ, respectively.

Singular Value Decomposition (SVD) Calculation and Error Analysis. For each member, i, of a set of twenty AC inhibitors, inhibitory potency, K_i, was modeled as the sum of the contributions, _i(j), of the two or three equally weighted chemical functional groups of which the inhibitor is composed:

(1)

where f_j is equal to 1/2 or 1/3 for nucleotide inhibitors that comprise two or three functional moieties (j), respectively. All of the nucleotide inhibitors in the data set contain at least two independent components: a nucleoside moiety and a (poly)phosphate group. A 2'(3')-O-ribosyl substituent constitutes the third functional component that is present in most of the inhibitors in the data set. The _i(j) comprise a set of 13 independent variables, which, in combinations of two or three, describe all members of the experimental data set. Five components, _i(j), correspond to contributions from possible phosphate functional groups (mono-, di-, tri-phosphate, -[thio]triphosphate, and (-imidino)triphosphate), six to nucleoside moieties (adenine, guanine, cytidine, uracil, hypoxanthine, and xanthine nucleoside), and two contributions to the 2'(3')-O-ribosyl substituents, MANT and TNP. K_i values for 20 inhibitors were experimentally determined in this study, or in published work (Table S1). The experimental data set of inhibition constants for 20 compounds was modeled in a system of 20 equations (eq. 1) in 2 to 3 of 13 variables, as follows:

Least-squares fit of the 13 _i values to eq. 2 was carried out by singular value decomposition (SVD) (Press et al., 1992; Gray, 1997). The data matrix was decomposed as the product of two orthonormal matrices and a pseudo-diagonal matrix. Equation 1 was recast as log[K_i(i)] = N_ij log[_i(j)], where K_i(i), i = 1 to 20, are the measured AC inhibition K_i values for the 20 dependent inhibitors, the _i(j) are the values of two or three of the possible 13 independent components that constitute compound (i), and the elements N_ij are set to 1 if the jth independent component is present in the ith inhibitor and to 0 otherwise. SVD of N_ij/_i gives USV^t (_i is the standard deviation of log[K_i(i)] derived from nonlinear regression of log[K_i(i)] versus AC activity. It is noted that 20% of log[K_i] value was used as standard deviation for those inhibitors from Gille et al. (2004). S is a diagonal jx j matrix of singular values for the set of independent components. The columns of the 20 x j matrix U are orthonormal basis vectors that together with the significant values of S and the corresponding rows of the jx j matrix V^t (where t denotes the transpose) provide the best least-squares approximation to the original matrix N_ij/_i. The values of log[_i(j)] were obtained from log[_i(j)] = (VS⁺U^t) x log[K_i(i)]/_i, as described previously (Press et al., 1992; Mou et al., 1999). Finally, substituting these values in eq. 2 gave the best-fit independent component values for the 13 values of log[_i(j)], from which calculated K_i(i) were obtained. These best-fit values could be compared with the experimentally determined K_i(i) values. A statistical test of the fit of the models is given by the probability Q (Press et al., 1992) that the ² value (where ² =_i|(log[K_imeas(i)] -log[K_i- _calc(i)])/_i|²) from the fit to the data would be larger by chance. A larger value of Q indicates a better fit. Values of Q > 0.1 are adequate and may be acceptable above 0.001 (Press et al., 1992).

	Results

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Inhibition of VC1:IIC2 by MANT Nucleotides and TNP Nucleotides. As was reported previously (Gille et al., 2004; Mou et al., 2005), MANT-ATP and MANT-GTP inhibited the catalytic activity of VC1:IIC2 that was maximally stimulated by FSK, GTPS-bound G_s and Mn²⁺, with K_i values in the 10 nM range (Table 1). However, when the linker between the MANT group and the ribosyl moiety was elongated to an aminoethyl-carbamoyl group, inhibitor potency at the fully activated VC1:IIC2 enzyme decreased approximately 500-fold. Translocation of the MANT group from the 2',3'-O-ribosyl position to the N6-position (6-MANT-ATP) or N8 position (MABA-ATP and MAHA-ATP) of the adenine ring was also poorly tolerated in terms of potency. Extension of the linker between the adenine ring and MANT from butyl to hexyl (MABA-ATPMAHA-ATP) was particularly detrimental to inhibitor potency.

TNP nucleotide triphosphates are moderately potent inhibitors of VC1:IIC2, with K_i values in the 100 nM range (Table 1). Like 2',3'-MANT nucleotides, 2',3'-TNP nucleotides are fluorescent (Hiratsuka, 2003). However, a major difference between MANT- and TNP nucleotides is that the TNP group is linked to both the 2'- and 3'-O-ribosyl atoms, preventing isomerization of the fluorophore and yielding a more defined but also more rigid molecule. Compared with MANT-ATP and MANT-GTP, TNP-ATP and TNP-GTP were approximately 7-fold less potent inhibitors of the fully activated VC1:IIC2 enzyme. Nonetheless, given their rigid structures, the potency of TNP-ATP and TNP-GTP was still very remarkable. In fact, the affinity of TNP-ATP and TNP-GTP for VC1:IIC2 is among the highest reported for targets of TNP nucleotides (Hiratsuka, 2003). It was also very remarkable that the pyrimidine nucleotide TNP-UTP exhibited nearly the same affinity for VC1:IIC2 as the purine nucleotides TNP-ATP and TNP-GTP. Exchange of uracil for cytidine, another pyrimidine base, reduced inhibitor potency 3-fold; nonetheless, the affinity of TNP-CTP for VC1:IIC2 surpassed that of TNP nucleotides for most other known target proteins (Hiratsuka, 2003). Elimination of the -phosphate in TNP-ATP, yielding TNP-ADP, reduced inhibitor-affinity 16-fold, and the elimination of the -phosphate, yielding TNP-AMP, reduced inhibitor-affinity by an additional 13-fold. For TNP-GTP, the effect of elimination of the -phosphate was even more pronounced, with a 100-fold reduction in affinity.

We also determined the potencies of nucleotides at inhibiting the submaximally activated VC1:IIC2 enzyme (i.e., the enzyme in the presence of FSK and Mn²⁺ but in the absence of activated G_s. Under these conditions, the potencies of MANT-GTP, MANT-ATP, and TNP-GTP were up to 10-fold lower, whereas the affinity of TNP-CTP was 3-fold higher. For the other nucleotides, the omission of activated G_s had little effect on inhibitor potency.

Fluorescence Analysis of the Interaction of MANTGTP and MANT-ATP with VC1:IIC2. In a previous study, we showed that the MANT group of MANT-GTP intercalates into a hydrophobic pocket between VC1 and IIC2, giving rise to increased nucleotide fluorescence at _ex = 350 nm (Mou et al., 2005). This fluorescence was further enhanced by the addition of the AC activator MP-FSK. Moreover, we observed FRET from Trp1020 of IIC2 to the MANT-group of MANTGTP at _ex = 280 nm.

At _ex = 350 nm, both MANT-GTP and MANT-ATP were excited to emit light with a maximum at _em = 450 nm (Fig. 1, B and D). Upon addition of VC1:IIC2, the fluorescence of both MANT-GTP and MANT-ATP was increased, but the fluorescence increase with MANT-GTP was larger than with MANT-ATP. Addition of MP-FSK to samples further enhanced fluorescence; again, the fluorescence increase with MANT-GTP was larger than with MANT-ATP. Moreover, we noted that with MANT-GTP, the emission peak was shifted to shorter wavelengths than with MANT-ATP, indicating that the MANT group in MANT-GTP resided in a more hydrophobic environment than the MANT group of MANTATP (Mou et al., 2005).

As reported earlier (Mou et al., 2005), we observed FRET from Trp1020 of IIC2 to the MANT-group of MANT-GTP at _ex = 280 nm. At this wavelength, both MANT-GTP and MANT-ATP alone in solution showed only minimal fluorescence (Fig. 1, A and C). Upon addition of VC1:IIC2, large fluorescence signals with a peak at _ex = 350 nm were observed, corresponding to the endogenous tryptophan fluorescence of the protein. It should be noted that the shape of the emission spectra at _ex = 280 nm was different for MANTGTP and MANT-ATP. In particular, the spectrum in the presence of MANT-ATP was steeper than in the presence of MANT-GTP (Fig. 1, compare green traces with the black dashed lines showing endogenous VC1:IIC2 tryptophan fluorescence in the absence of MANT nucleotides). These data are indicative of FRET from Trp1020 of IIC2 to the MANT group of MANT-GTP, but not to the MANT group of MANTATP. Upon the addition of MP-FSK, the emission peak at _em = 350 nm was moderately decreased in the presence of MANT-GTP, and an additional fluorescence peak with a maximum at _em = 420 nm appeared. These data are indicative of enhanced FRET from Trp1020 to MANT-GTP. In contrast, only a very small decrease of the fluorescence peak at _em = 350 nm was observed upon the addition of MP-FSK to the MANT-ATP-inhibited enzyme, and there was virtually no fluorescence increase at _em = 420 nm, showing that FRET does not occur in this complex.

Crystal Structures of TNP-ATP ·Mn²⁺ and MANTATP · Mn²⁺ Complexes. The similar inhibitory potencies of MANT-GTP and MANT-ATP toward VC1:IIC2 (Table 1), despite their different fluorescent properties upon interaction with VC1:IIC2 (Fig. 1), prompted us to compare the X-ray crystal structures of VC1:IIC2 bound to MANT-ATP with that of the complex of MANT-GTP, which was reported earlier (Mou et al., 2005). The remarkably high potencies of TNP nucleotides at inhibiting VC1:IIC2 (Table 1) led us to determine the X-ray crystal structure of VC1:IIC2 bound to TNP-ATP as well. Structures of G_s ·GTPS ·VC1:IIC2 ·MPFSK protein complexes with TNP-ATP ·Mn²⁺ and MANTATP ·Mn²⁺ were determined at 2.9- and 3.3-Å resolution, respectively. The 2|F_o| -|F_c| difference maps computed for crystals soaked in Mn²⁺ and TNP-ATP or MANT-ATP showed clearly interpretable electron density around the substrate-binding site (Fig. 2). Table 2 provides a summary of the crystallographic data collection and refinement statistics. The purine riboside and triphosphate moieties of both inhibitors occupy the same subsites observed for the corresponding groups of other ATP analogs (Tesmer et al., 1997, 1999, 2000), and their 2',3'-ribosyl substituents bind to the previously recognized MANT binding pocket at the C1:C2 interface (Mou et al., 2005). Difference |F_o| -|F_c| electron density for metal ions at the A and B sites is observed in both structures and is stronger than that in complexes in which only Mg²⁺ is present (data not shown), indicating that Mn²⁺ replaced Mg²⁺ at both sites. The two metal ions coordinate the 5'-triphosphates of 2',3'-ribosyl-substituted ATP, and their protein ligands occupy roughly the same positions seen in complexes with MANT-GTP or un-/noncompetitive AC inhibitors (so-called P-site inhibitors) (Dessauer et al., 1999). However, the average temperature factors (B-factors) of TNP-ATP ·Mn²⁺ and MANT-ATP ·Mn²⁺ are 71 and 90 Ų and higher than those of the other ligands in the structure, MPFSK and GTPS, which are 34 and 41 Ų, respectively. Therefore, we infer that the ATP analogs are less well ordered than the latter two ligands. Given the diffraction limits of the crystals of the two complexes, it is also possible that the high B-values reflect only partial occupancy of the catalytic site of C1:C2 by TNP-ATP and MANT-ATP. Because of the modest resolution of the data, combined with high B-factors of the ATP analogs, hydrogen bond interactions in the MANT-ATP ·Mn²⁺-bound complex cannot be unambiguously assigned.

View larger version (65K): [in this window] [in a new window]   Fig. 2. Electron densities of TNP-ATP and MANT-ATP in the catalytic site of VC1:IIC2. The complexes formed with TNP-ATP (A) and MANTATP (B) in the presence of Mn2+ at 2.9- and 3.3-Å resolution, respectively. The models of the inhibitors are shown in ball-and-stick representation, and the individual electron density surrounding each ligand, shown in lime-green wire cage, is a 2|Fo| -|Fc| difference map calculated at the respective final resolution and contoured at the 1.2 level.

We reported previously that the MANT fluorophore of MANT-GTP hampered the movement of the 1-1-2 loop of C1 and the 4'-5' and 7'-8' loops of C2 from the inactive (open) conformation to the active (closed) conformation (Mou et al., 2005) (Fig. 3, A and D). The TNP moiety of TNP-ATP (Figs. 2A and 3B) and the MANT substituent of MANT-ATP (Figs. 2B and 3C) occupy the same binding pocket at the C1:C2 interface and similarly prevent full domain closure. The overall pairwise root-mean-square deviations between corresponding C atoms of TNP-ATP ·Mn²⁺, MANTATP ·Mn²⁺, and MANT-GTP ·Mn²⁺ complexes are less than 0.6 Å, suggesting that the global conformational differences among these inhibitor-bound complexes are small. However, relative to complexes with potent inhibitors, such as -L-2',3'-dideoxy-5'-ATP, the catalytic site, particularly the purine binding subsite, is slightly enlarged as a result of the intercalation of the MANT or TNP substituent between the C1 and C2 domains.

View larger version (91K): [in this window] [in a new window]   Fig. 3. Views of crystal structures of Gs · VC1 ·IIC2 in complex with substrate analogs. A, a wide-range view of complex of Gs-activated mAC with TNP-ATP and two Mn2+ ions in the catalytic site. VC1, IIC2, and Gs are shown in mauve, tan, and gray, respectively. The 2 (switch II) helix of Gs is shown in red. MP-FSK, TNP-ATP and two metal ions occupy the interdomain cleft between the C1 and C2 domains. Secondary structure elements are labeled as defined previously (Tesmer et al., 1997). Detailed views of the substrate-binding site of VC1 ·IIC2 showing TNP-ATP (B), MANT-ATP (C), and MANT-GTP (PDB 1TL7) (D) and two Mn2+ ions, respectively. MP-FSK and nucleotide inhibitors are drawn as stick models; carbon atoms are gray, nitrogen is blue, oxygen is red, and phosphorus is green; the two Mn2+ ions are shown as metallic orange spheres. Single-letter amino acid abbreviations are presented with position numbers, and protein residues are shown as stick models. The ribose substituents of inhibitor molecules are positioned between the 4 helix of IIC2 and 1-2 helices of VC1. Interactions are shown among protein residues, inhibitors, and two metal ions in the VC1 ·IIC2 substrate-binding site. The gray dashed lines depict the hydrogen bonds between inhibitor molecules and protein residues, and coordination of the metal ions at sites A and B. Because of the high thermal parameters of the nucleotide (see text), hydrogen bond distances are approximate.

The conformations of TNP-ATP and MANT-ATP and their interactions with VC1:IIC2 residues in the substrate-binding site are illustrated in Fig. 3, B and C, respectively. The structure of the MANT-GTP ·Mn²⁺ complex is also shown in Fig. 3D for comparison. The positions and orientations of 3'-MANT or 2',3'-TNP substituents of ATP are similar to that of 3'-MANT of GTP in the binding groove between 1-1-2 of VC1 and 4'-5' of IIC2. The MANT groups of both MANT-ATP and MANT-GTP are in van der Waals contact with VC1 and IIC2 but do not form hydrogen bonds with neighboring protein residues. This binding pocket contains a group of conserved nonpolar residues including Trp1020 of IIC2 and two residues, Ala409 of VC1 and Ile1006 of IIC2, that are not conserved among the type I-VIII mAC isoforms (Mou et al., 2005). Substitution of Ala409 of VC1 with proline and/or Ile1006 of IIC2 with valine reduces the inhibitory potency of MANT-GTP to mAC by 2- to 10-fold, indicating that these nonconserved residues in the MANT binding pocket influence the affinity of mAC for inhibitors with 3'-MANT substituents. In the TNP-ATP ·Mn²⁺ complex, the TNP substituent of ATP is bound to the same pocket that is occupied by the MANT group of the inhibitors described above. The two polar NH₂ groups of TNP seem to form hydrogen bonds with the carboximido NH₂ groups of Asn1022 and Asn1025 of IIC2 and the backbone oxygen of Ala409 of VC1 (Figs. 3B and 4E). These hydrogen bonds are presumed to stabilize the TNP ring in the VC1:IIC2 substrate-binding site.

View larger version (45K): [in this window] [in a new window]   Fig. 4. General pharmacophore model of the mAC inhibitors. A, an overview of Gs ·VC1:IIC2-inhibitor complexes, shown with the inhibitors superimposed. Carbon atoms are yellow for TNP-ATP, cyan for MANTATP, and gray for MANT-GTP in the VC1 and IIC2 protein interface. Mn2+ and FSK/MP-FSK are colored according to the respective ligand in the complex. Atoms are otherwise colored as described in the legend to Fig. 3. The molecular surface was calculated using the program PYMOL (DeLano Scientific, San Carlos, CA), based on the atomic coordinates of the Gs ·VC1:IIC2 ·TNP-ATP complex. B, structures of MANT-ATP, MANT-GTP, and TNP-ATP, as bound to their respective complexes with Gs ·VC1:IIC2 are superimposed and colored as in A. C, a general pharmacophore model of the mAC inhibitors from B with three functional groups, nucleotide base, blue; phosphate, green; 2',(3')-O-ribose substituent, gray. Overall i values that represent the contribution of each type of functional group are indicated, computed from the mean of ln(i) values for that group from Table 3. The latter were derived from SVD of the set of relationships given by eq. 1. The xanthine and monophosphate nucleotides were excluded from the averaging i values for their apparently unfavorable contributions to the respective pharmacophore. D, a detailed schematic of base centers in the VC1:IIC2 purine-binding pocket. Hydrogen bonds between base (adenine group of TNP-ATP and guanine group of MANT-GTP) and neighboring IIC2 protein residues are shown in dashed lines. E, base substituent centers of inhibitors in the VC1:IIC2 substrate-binding site. Only the 2,4,6-trinitrophenyl substituent of TNPATP and the 2'-ribosyl OH of MANT-GTP form hydrogen bonds with VC1 and IIC2 protein residues.

The three derivatives differ greatly in the coordination of their poly-phosphate chains with neighboring protein residues and metal ions. In particular, the positions occupied by the - and -phosphates of TNP-ATP are very close to those taken by the corresponding phosphates of -L-2',3'-dideoxy-5'-ATP and adenosine 5'-[-thio]triphosphate but correspond to the binding sites of the - and -phosphates of MANT-ATP and MANT-GTP. As a result, Lys484 of VC1 can interact with the -phosphate of TNP-ATP (as in the complex with -L-2',3'-dideoxy-5'-ATP) but not with the -phosphate of MANT-GTP (Fig. 3, B-D). Lys1065 from 7'-8' of IIC2 interacts with a -phosphate oxygen and the - bridging oxygen of TNP-ATP. The same interaction is observed with the corresponding atoms in the MANT-GTP complex (Fig. 3, B and D). Metal B is essential for stabilizing the ligand through an octahedral coordination with the oxygen atoms of two phosphates and three VC1 residues (Asp396, Ile397, and Asp440) in both TNP-ATP ·Mn²⁺ and MANT-GTP ·Mn²⁺ complexes (Fig. 2). Conversely, in the TNP-ATP ·Mn²⁺ complex, metal A is coordinated by the two aspartate residues (Asp396 and Asp440) from VC1, but not with the - or -phosphates as observed in the MANT-GTP ·Mn²⁺ complex (Figs. 2A and 3D). It should be noted that both TNP-ATP · Mn²⁺ and MANT-ATP ·Mn²⁺ complexes were cocrystallized with MPFSK rather than FSK. The 7-acetyl-7-[O-(N-methylpiperazino)--butyryl] moiety of this ligand is bound closely to, but makes no direct contact with, the metal-A site (Figs. 2 and 3) in either structure.

The MANT and TNP nucleotide complexes show that the substrate-binding site of mAC is able to accommodate different purine substituents. It is remarkable that the purine moieties of TNP-ATP and MANT-ATP are bound to the same mAC subsite in completely different orientations (Fig. 4, A and D). The base of TNP-ATP adopts an anti conformation ( = 234°) with respect to the ribose ring as observed for the guanine ring of MANT-GTP, but MANT-ATP adopts the syn orientation ( = 64°), which is similar to that observed for other ATP analogs (Mou et al., 2005). Whereas the N6 and N7 atoms in the adenine ring of TNP-ATP form hydrogen bonds to Ser1028 of IIC2 (Fig. 3B), there are no apparent hydrogen bond interactions between the adenine ring of MANT-ATP and protein residues. The adenine moiety of MANT-ATP is observed at a position that is intermediate between the purine rings of MANT-GTP and TNP-ATP in the base-binding pocket (Fig. 4, A and D). Therefore, the potency for AC inhibitors containing 2',3'-ribosyl substituents is not greatly determined by their nucleoside base, as is discussed below.

	Discussion

Top Abstract Materials and Methods Results Discussion References

 
The three independent X-ray crystal structures of VC1: IIC2 in complex with 2',3'-ribose-substituted nucleotide AC inhibitors reported here and previously (Mou et al., 2005) reveal common features that we propose to be essential for their potency. A general tripartite pharmacophore model for catalytic site-targeted mAC inhibitors can be derived from the structural data and is supported by a systematic enzymatic analysis of natural and modified purine and pyrimidine nucleotides (Gille et al., 2004, 2005; Mou et al., 2005) (Fig. 4, B and C, and Table 1). The inhibitor site, which overlaps the binding site for the substrate ATP, contains a deep hydrophobic pocket for a 2',3' ribose substituent, a polar phosphate-binding groove adjacent to the catalytic Mn²⁺-binding site, and a spacious base-binding pocket (Fig. 4A). Superposition of the three potent inhibitors MANT-GTP, TNP-ATP, and MANT-ATP in the AC substrate binding site (Fig. 4) shows that the ribose substituents and triphosphate group (in coordination with two metal ions) are nearly aligned, but the base rings of these molecules are not.

Complementarity between the ribose-substituent and its binding pocket is essential for high-affinity binding. We previously showed that incorporation of a MANT group at the 3'-position of inosine 5'-[-thio]triphosphate increased inhibitory potency 60-fold (Gille et al., 2004). However, potency is decreased up to 40-fold relative to inosine 5'-[-thio]triphosphate when the ribose is substituted with a larger bulky BODIPY group, demonstrating the size-selectivity of the binding site for the ribose substituent of the inhibitor (Gille et al., 2004; Mou et al., 2005). In the present study, we show that substitution of UTP or CTP with 2',3'-TNP increases the affinity of these pyrimidine nucleotides by up to 20,000-fold (Table 1) (Gille et al., 2005). Substitution of ATP with 2',3'-aminoethyl-carbamoyl-MANT instead of MANT decreases potency up to 500-fold (Table 1), again confirming the size-selectivity of the pocket that accommodates the ribose substituent.

Several nonpolar residues conserved among mAC isoforms, including Trp1020 of IIC2, create a hydrophobic surface in the binding pocket for the ribose substituent (Mou et al., 2005). The increase in MANT fluorescence upon binding of MANT-GTP and MANT-ATP, or of FRET from MANT to Trp1020 (Fig. 1), is consistent with the interaction of the fluorophore with this hydrophobic pocket. Formation of hydrogen bonds between the NO₂ substituents of the trinitrophenyl group and polar groups in the binding site is probably crucial for the moderately high inhibitory potency of TNP-substituted nucleotides (Fig. 4E).

The nucleotide triphosphates that coordinate the two metal cofactors also provide substantial binding energy for interaction with VC1:IIC2. During catalysis, both metal ions play critical roles in ATP binding by coordinating the 3'-hydroxyl and 5'-triphosphate of ATP and neighboring protein residues around the catalytic core (Tesmer et al., 2000). Metal-B coordinates with the - and/or -phosphate(s) of ATP analogs in the C1:C2 binding site (Tesmer et al., 1999, 2000; Mou et al., 2005) (Fig. 2B). Elimination of the -phosphate or - and -phosphates of TNP-ATP reduce its affinity for VC1: IIC2 by approximately 20- and 200-fold, respectively (Table 1). The -phosphate is important for high binding affinity of TNP-GTP as well. The -phosphates of MANT-ATP and MANT-GTP also contribute at least 4-fold to their potency relative to the corresponding nucleotide diphosphates (Gille et al., 2004). The crystallographic data unequivocally demonstrate that the Mn²⁺ ion in the A-site coordinates with the -phosphate of MANT-substituted nucleotides, but not with that of TNP-ATP (Fig. 2A). Therefore, at least one metal ion at B site is essential to coordinate and stabilize the polyphosphate chain in the binding groove.

We have used SVD to quantitatively compare the contributions to inhibitory potency from the independent functional groups in a set of 2',3'-ribose-substituted nucleotide AC inhibitors. A relationship (eq. 1) was developed to express the K_i values of these compounds in terms of contributions from two to three chemical components corresponding to the base, phosphate, and 2'(3')-O-ribosyl substituent. The data set of 20 inhibitors (Table 3) encompasses 13 variations of these three components (see Materials and Methods). SVD of the matrix of twenty equations corresponding to the inhibitor set (eq. 2) provides the least-squares fit of the observed K_i values to the thirteen independent affinity components _i that encompass the chemical variation among inhibitors. The _i values can be used to reconstitute computed K_i values that are comparable in magnitude with the observed set (Table 3; see Table 1 in the supplementary material). This analysis shows that the 2'(3')-O-ribosyl substituent (MANT or NP) contributes 20-fold more to inhibitory potency than the phosphate group and nearly 1000-fold more than the base, as illustrated in the schematic shown in Fig. 4C. Although the data allowing comparison of the effects of MANT- and TNP-substitution of nucleotide di- and triphosphates are limited to adenine and guanine nucleotides (Table 1 of this study and Table 1 of Gille et al., 2004), it is evident that MANT substitution contributes more to potency than derivatization by TNP (Table 3).

Introduction of a bulky, aromatic group at the ribose 2' and 3' positions of ATP generates a class of mAC inhibitors that are resistant to hydrolysis and use a subsite at the interface of the C1 and C2 domains that is not present in the catalytically active conformation of the enzyme. The structures of complexes formed with such inhibitors indicate that the base-binding site is slightly enlarged, perhaps as a result of local distortions induced by binding of the MANT or TNP ribose substituent. Therefore, the specificity of base binding site for purines is relaxed relative to that of the active conformation of the enzyme, and specific interactions between the base and the base binding site have little influence on affinity for the inhibitor. For the MANT- and TNP-substituted nucleotides, binding energy not realized at the base binding site is recovered from interactions with the ribose substituent. Structures of a variety of C1:C2 complexes with ATP analogs and P-site inhibitors show that there is considerable variation in the mode of interaction between VC1:IIC2 and 5'- or 3' phosphate groups and pyrophosphate, although similar patterns of metal cation and hydrogen bond recognition are observed in all complexes (Tesmer et al., 2000). The MANT/TNP nucleotide inhibitors take advantage of the plasticity of the phosphate binding site in forming interactions that optimize interactions at all subsites. Because mAC is deformable at the interface between its catalytic domains, the enzyme exhibits broad specificity for interaction with purine and pyrimidine nucleotides. MANT/TNP nucleotide inhibitors represent a novel class of potent mAC inhibitors in which relatively nonspecific yet energetically productive ionic van der Waals and hydrogen bonding interactions at three distinct subsites contribute to binding affinities in the 10 to 100 nM range. These compounds may be therefore viewed as lead compounds for the development of mAC isoform-specific, potent, and bioavailable inhibitors.

	Acknowledgements

 
We thank Dr. Donald Gray and Tzu-Fang Lou (University of Texas at Dallas), and Arne Strand for extensive discussion on SVD calculations. We also thank the staff at the Advanced Light Synchrotron 8.2.1 beamline (Berkeley, CA) for their assistance with data collection.

	Footnotes

 
This work was supported by National Institutes of Health grant DK46371 (to S.R.S.), Welch Foundation grant I-229 (to S.R.S.), the John W. and Rhoda K. Pate Professorship (to S.R.S.), grant 0450120Z from the Heartland Affiliate of the American Heart Association (to R.S.), the Graduate Training Program (Graduiertenkolleg) 760 "Medicinal Chemistry: Molecular Recognition-Ligand-Receptor Interactions" of the Deutsche Forschungsgemeinschaft (to R.S.), and a predoctoral fellowship from the Studienstiftung des Deutschen Volkes (to A.G.).

ABBREVIATIONS: AC, adenylyl cyclase; mAC, membrane-bound adenylyl cyclase; G_s, stimulatory G-protein for mAC; FSK, forskolin; MP-FSK, 7-acetyl-7-[O-(N-methylpiperazino)--butyryl)]-forskolin; VC1 and IIC2, the N- and C-terminal catalytic domains from canine type V mAC and rat type II mAC, respectively, expressed as soluble proteins; GTPS, guanosine 5'-[-thio]triphosphate; SVD, singular value decomposition; FRET, fluorescence resonance energy transfer; MABA, 8-[(4-(N-methylanthraniloyl)amino)butyl]amino; MAHA, 8-[(6-(N-methylanthraniloyl)amino)hexyl]-amino; MANT, 2'(3')-O-(N-methylanthraniloyl); 6-MANT, N⁶-[6-((N-methylanthraniloyl)amino)hexyl]; MANT-EDA, 2,3,-[(2-(N-methylanthraniloyl)amino)ethyl-carbamoyl]; TNP, 2',3'-O-(2,4,6-trinitrophenyl).

The online version of this article (available at http://molpharm.aspetjournals.org) contains supplemental material.

¹ Current affiliation: Department of Pharmacology, University of Heidelberg, Heidelberg, Germany.

Address correspondence to: Dr. Stephen R. Sprang, Department of Biochemistry, The University of Texas Southwestern Medical Center at Dallas, Dallas, TX 75390-9050 E-mail: stephen.sprang{at}utsouthwestern.edu

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