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GASTROINTESTINAL, HEPATIC, PULMONARY, AND RENAL
Digestive Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland (S.A.M., L.K.E., R.T.J.); and Peptide Research Laboratories, Department of Medicine, Tulane University Health Sciences Center, New Orleans, Louisiana (D.H.C.)
Received February 9, 2004; accepted April 20, 2004.
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Abstract |
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-Ala11,Phe13,Nle14]Bn(6-14), has been described, but it is nonselective for hBRS-3 over other Bn receptors; however, substitution of (R)- or (S)-amino-3-phenylpropionic acid (Apa) for -Ala11 resulted in a modestly selective ligand. In the present study, we have attempted to develop a more selective hBRS-3 ligand by using two strategies: substitutions on phenyl ring of Apa11 and the substitution of other conformationally restricted amino acids into position 11 of [D-Tyr6,-Ala11,Phe13,Nle14]Bn(6-14). Fifteen analogs were synthesized and affinities were determined for hBRS-3 and Bn receptors (hGRP-R and hNMB-R). Selective analogs were tested for their ability to activate each receptor by stimulating phospholipase C. One analog, [D-Tyr6,Apa-4Cl,Phe13,Nle14]Bn(6-14), retained high affinity for the hBRS-3 (Ki = 8 nM) and had enhanced selectivity (>230-fold) for hBRS-3 over hGRP-R or hNMB-R. This analog specifically interacted with hBRS-3, fully activated hBRS-3 receptors, and was a potent agonist at the hBRS-3 receptor. This enhanced selectivity should allow this analog to be useful for investigating the possible role of hBRS-3 in physiological or pathological processes.
; Fathi et al., 1993; Ohki-Hamazaki et al., 1997a; Whitley et al., 1999; Liu et al., 2002). BRS-3 is widely expressed in the rat central nervous system and is present in a few peripheral tissues, although its distribution is species-dependent and much more limited than the GRP-R or NMB-R (Tache et al., 1988; Fathi et al., 1993; Ohki-Hamazaki et al., 1997a; Whitley et al., 1999; Liu et al., 2002; Jennings et al., 2003). BRS-3 is reported to occur in human islets (Fleischmann et al., 2000); in the testes of the rat, but not mouse, human, or sheep; and in the guinea pig and human uterus, but not mouse or sheep uterus (Gorbulev et al., 1992, 1994; Fathi et al., 1993; Ohki-Hamazaki et al., 1997a; Whitley et al., 1999; Liu et al., 2002). Recent studies show it is also expressed on small cell lung cancer, lung carcinoid tumors, ovarian, breast, and prostate cancer (Gorbulev et al., 1992; Fathi et al., 1993; Sun et al., 2000a,b; Reubi et al., 2002).
The natural ligand of BRS-3 is unknown and its role in physiological and pathological processes is largely unknown. However, in recent studies, BRS-3 knockout mice developed obesity, diabetes, and hypertension (Ohki-Hamazaki et al., 1997b), suggesting the BRS-3 receptor was involved in regulation of blood pressure, glucose metabolism, and energy balance. This proposal is supported by the recent finding that BRS-3 regulates insulin release (Matsumoto et al., 2003). The elucidation of the role of BRS-3 in various physiological/pathological processes has been limited by the lack of availability of high-affinity ligands that activate or antagonize the action of this receptor. hBRS-3 has a unique pharmacology and despite its high homology to mammalian Bn receptors, none of the naturally occurring high-affinity ligands for these receptors had high affinity for BRS-3 (Gorbulev et al., 1992; Fathi et al., 1993; Wu et al., 1996; Mantey et al., 1997; Ryan et al., 1998a,b). However, we have recently found the synthetic ligand [D-Tyr6,-Ala11,Phe13,Nle14]Bn(6-14) functioned as a high-affinity agonist at the hBRS-3 receptor (Mantey et al., 1997; Pradhan et al., 1998; Ryan et al., 1998a,b). Using this ligand and its derivative, it has been possible to explore the pharmacology as well as the cellular transduction cascades of the hBRS-3 (Mantey et al., 1997; Pradhan et al., 1998; Ryan et al., 1998a,b). These studies confirm the unique pharmacology of hBRS-3 with low affinity for all known naturally occurring agonists for all Bn receptors (GRP-R, NMB-R, and bombesin receptor subtype 4) (Mantey et al., 1997; Pradhan et al., 1998; Ryan et al., 1998a,b) as well as demonstrate that hBRS-3 activation is coupled to a phospholipase C, changes in cytosolic calcium, mitogen-activated protein kinase activation, immediate oncogene activation (e.g., c-fos), and activation of other tyrosine kinases (e.g., p125FAK) (Fathi et al., 1993; Wu et al., 1996; Ryan et al., 1998a,b, 1999; Weber et al., 2001). Unfortunately, the usefulness of [D-Tyr6,-Ala11,Phe13,Nle14]Bn(6-14) to study the role of hBRS-3 in various processes is limited because recent studies show it has a high affinity for all human Bn receptor subtypes and is nonselective (Mantey et al., 1997; Pradhan et al., 1998; Ryan et al., 1998a, 1999; Katsuno et al., 1999; Reubi et al., 2002). In a recent study (Mantey et al., 2001), in an attempt to develop more selective hBRS-3 ligands, the -Ala in [D-Tyr6,-Ala11,Phe13,Nle14]Bn(6-14) was replaced by different conformationally restricted amino acids and two peptides with an (R)- or (S)-amino-3 phenylpropionic (Apa) substitution for -Ala11 had some selectivity for the hBRS-3. However, this selectivity was modest for differential receptor activation because of the marked difference in receptor spareness for hBRS-3 and the different Bn receptors, limiting their potential utility.
Therefore, the aim of the present study was to attempt to identify a more selective hBRS-3 ligand. Two strategies were used. First, modification of the phenyl ring of the Apa11 of the moderately selective ligand [D-Tyr6,(R) or (S)Apa11,Phe13,Nle14]Bn(6-14), and second, replacement of the Apa11 with other conformationally restricted amino acids. Using the first approach, we identified a ligand with enhanced selectivity for hBRS-3 that could be useful for exploring its role in various processes.
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Materials and Methods |
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-6-diphenylglycouril was from Pierce Chemical (Rockford, IL); AG 1-X8 resin was from Bio-Rad (Hercules, CA); and Bn, GRP, NMB, and [Tyr4]Bn were from Bachem California (Torrence, CA). Standard, protected amino acids and other synthetic reagents were obtained from Bachem Biosciences (King of Prussia, PA). Boc(R)-3 amino-3-[4-chlorophenyl] propionic acid (Apa-4Cl), Boc(R)-3 amino-3-[3-chlorophenyl]propionic acid (Apa-3Cl), Boc(R)-3 amino-3-[2-chlorophenyl]propionic acid (Apa-2Cl), Boc--aspartic acid (-Asp), Boc--aspartic acid benzilamide (-AspBzlAmd)), Boc-2,3-diamino propionic acid (-Dap), Boc-2-acetylamino, 3-amino propionic acid (N-acetyl-Dap), Boc-2-benzoylamino, and 3-amino propionic acid (N-benzoyl-Dap) (Fig. 1) were purchased from ChiroTech (Cambridge, UK). All chemicals were reagent grade.
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Cell Culture. Balb/c 3T3 cells stably expressing human BRS-3 receptors, human NMB receptors, or human GRP receptors were made as described previously (Mantey et al., 1993, 1997; Ryan et al., 1998a) and grown in Dulbecco's modified Eagle's medium supplemented with 10% FBS and 300 mg/l G418 sulfate. CHO cells stably expressing human vasoactive intestinal peptide receptor subtype 1 (hVIP1-R) and subtype 2 (hVIP2-R) were made as described previously (Ito et al., 2000; Igarashi et al., 2002a,b) and grown in Ham's F-12K media supplemented with 10% FBS and 300 mg/l G418 sulfate. AR42J cells were grown in Dulbecco's modified Eagle's medium supplemented with 10% FBS. All cells were incubated at 37°C in a 5% CO2 atmosphere.
Preparation of Peptides. Peptides were synthesized with solid-phase methods as described previously (Sasaki and Coy, 1987; Wang et al., 1990; Mantey et al., 2001). Briefly, solid-phase syntheses of peptide amides were carried out using Boc chemistry on methylbenzhydrylamine resin (Advanced ChemTech, Louiville, KY) followed by HF-cleavage of free peptide amides. The crude peptides were purified, and in some cases separated into R-isomers and S-isomers by preparative high-pressure liquid chromatography on columns (2.5 x 50 cm) of Vydac C18 silica (10 µm), which was eluted with linear gradients of acetonitrile in 0.1% (v/v) trifluoroacetic acid. Homogeneity of the peptides was assessed by analytical reverse-phase high-pressure liquid chromatography, and purity was usually 97% or higher. Amino acid analysis (only amino acids with primary amino acid groups were quantitated) gave the expected amino acid ratios. Peptide molecular masses were obtained by matrix-assisted laser desorption mass spectrometry (Lasermat; Thermo Finnigan, San Jose, CA), and all corresponded well with calculated values.
Preparation of 125I-[D-Tyr6,-Ala11,Phe13,Nle14]Bn(6-14), 125I-[Tyr4]Bn, and 125I-[D-Tyr0]NMB. These radioligands, with specific activities of 2200 Ci/mmol, were prepared as described previously (Mantey et al., 1993, 1997, 2001). Briefly, 0.8 µg of 1,2,4,6-tetrachloro-3-6-diphenylglycouril solution (0.02 µg/µl in chloroform) was added to a 5-ml plastic test tube, dried under nitrogen, and washed with 100 µl of 0.5 M potassium phosphate solution (pH 7.4). To this tube 20 µl of potassium phosphate solution (pH 7.4), 8 µg of peptide in 4 µl of water, and 2 mCi (20 µl) of Na125I were added and incubated at room temperature for 6 min. The incubation was stopped by the addition of 100 µl of water and heated with 300 µl of 1 M dithiothreitol for 60 min at 80°C. I125-[D-Tyr6,-Ala11,Phe13,Nle14]Bn(6-14), which does not have a COOH-terminal methionine group, was not incubated with the dithiothreitol. The radiolabeled peptides were separated using a Sep-Pak (Waters, Milford, MA) and further purified by reverse-phase high-performance liquid chromatography, as described previously (Mantey et al., 1993, 1997). The fractions with the highest radioactivity and binding were neutralized with 0.2 M Tris buffer (pH 9.5) and stored with 0.5% bovine serum albumin (w/v) at -20°C.
Binding of 125I-Labeled Peptides to Balb/c 3T3 Cells Transfected with hBRS-3, hGRP-R, or hNMB-R. Binding studies to Balb/c 3T3 cells transfected with human bombesin receptor subtypes were carried out as described previously (Benya et al., 1994, 1995; Mantey et al., 1997, 2001). Briefly, the standard incubation buffer contained 24.5 mM HEPES (pH 7.4), 98 mM NaCl, 6 mM KCl, 2.5 mM NaH2PO4, 5 mM sodium pyruvate, 5 mM sodium fumarate, 5 mM MgCl2, 0.01% (w/v) soybean trypsin inhibitor, 0.2% (w/v) bovine serum albumin, and 0.05% (w/v) bacitracin. Balb/c 3T3 cells transfected with hBRS-3 (0.5 x 106/ml), hGRP-R (0.2 x 106/ml), or hNMB-R (0.03 x 106/ml) were incubated with 50 pM 125I-labeled ligand at 22°C for 60 min. Aliquots (100 µl) were removed and centrifuged through 300 µl of 4°C incubation buffer in 400-µl Microfuge tubes at 10,000g for 1 min using a Microfuge B (Beckman Coulter Inc., Fullerton, CA). The pellets were washed twice with buffer and counted for radioactivity in a gamma counter. The nonsaturable binding was the amount of radioactivity associated with cells in incubations containing 50 pM of radioligand (2200 Ci/mmol) and 1 µM unlabeled ligand. Nonsaturable binding was <10% of total binding in all the experiments. Receptor affinities of ligands were determined using a least-square curve-fitting program (LIGAND) (Westendorf and Schonbrunn, 1983) and the Cheng-Prusoff equation (Cheng and Prusoff, 1973).
Binding of 125I-Ligands to Dispersed Rat Pancreatic Acini, AR42J Cells, and hVPAC1-R- and hVPAC2-R-transfected CHO Cells. Dispersed rat pancreatic acini (1 pancreas/10 ml), AR42J cells (1 x 106/ml), hVPAC1-R transfected into CHO cells (1.5 x 106/ml) (Ito et al., 2000; Igarashi et al., 2002a,b), and hVPAC2-R transfected into CHO cells (0.2 x 106/ml) (Ito et al., 2000; Igarashi et al., 2002a,b) were suspended in standard incubation solution with 0.05% (w/v) bacitracin. Dispersed acini from rat pancreas were prepared using collagenase digestion as described previously (Jensen et al., 1982; Garcia et al., 1997). Incubations with125I-somatostatin and 125I-BH-substance P contained phosphoramidon (10 mM), leupeptin (25 µg/ml), 4-(2-aminoethyl)-benzenesulfonyl fluoride (10 µM), and amastatin (10 mM). Incubations with the other ligands (125I-BHCCK-8 and 125I-PACAP) were at 37°C for 60 min with rat pancreatic acini and 23°C with AR42J cells or hVPAC-R-transfected cells. Binding was performed as described previously (Mantey et al., 1993, 1997, 2001; Ito et al., 2001; Igarashi et al., 2002a,b). Briefly, 50 pM radioligand was incubated with the cells alone or with 1 µM unlabeled other peptides at the specified concentrations or with 1 µM unlabeled ligand to determine saturable binding. Bound ligand was separated from free ligand by centrifugation. Tubes were washed twice with 2% (w/v) bovine serum albumin in standard incubation solution and radioactivity was counted. Nonsaturable binding was less than 30% of total binding.
Measurement of [3H]IP. Changes in total [3H]inositol phosphates ([3H]IP) were measured as described previously (Benya et al., 1992, 1994; Ryan et al., 1998a; Mantey et al., 2001). Briefly, hBRS-3, hGRP-R-, or hNMB-R-transfected Balb/c 3T3 cells were subcultured into 24-well plates (5 x 104 cells/well) in regular propagation media and then incubated for 24 h at 37°C in a 5% CO2 atmosphere. The cells were then incubated with 3 µCi/ml of myo-[2-2H]inositol in growth media supplemented with 2% FBS for an additional 24 h. Before assay, the 24-well plates were washed by incubating for 30 min at 37°C with 1 ml/well of phosphate-buffered saline (pH 7.0) containing 20 mM lithium chloride. The wash buffer was aspirated and replaced with 500 µl of inositol phosphate assay buffer containing 135 mM sodium chloride, 20 mM HEPES (pH 7.4), 2 mM CaCl2, 1.2 mM MgSO4, 1 mM EGTA, 20 mM LiCl, 11.1 mM glucose, and 0.05% bovine serum albumin (w/v) and incubated with or without any of the peptides studied. After 60 min of incubation at 37°C, the experiments were terminated by the addition of 1 ml of ice-cold 1% (v/v) hydrochloric acid in methanol. Total [3H]IP was isolated by anion exchange chromatography as described previously (Benya et al., 1992, 1994; Ryan et al., 1998a; Mantey et al., 2001). Briefly, samples were loaded onto Dowex AG1-X8 anion exchange resin columns, washed with 5 ml of distilled water to remove free [3H]inositol, and then washed with 2 ml of 5 mM disodium tetraborate/60 mM sodium formate solution to remove [3H]glycerophosphorylinositol. Two milliliters of 1 mM ammonium formate/100 mM formic acid solution was added to the columns to elute total [3H]IP. Each eluate was mixed with scintillation cocktail and measured for radioactivity in a scintillation counter.
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), but not avian (Iwabuchi et al., 2003), have low affinity for -Ala11 analogs of bombesin. At present, no selective or high-affinity ligands have been identified for the rat or mouse BRS-3 receptor. We first examined six analogs of [D-Tyr6,Apa11,Phe13,Nle14]Bn(6-14) with various position 11 chloro-substitutions (Table 1, peptides 4-9; Fig. 2). This strategy was performed because previous studies in a number of G protein-coupled receptors demonstrated that insertions of electron-withdrawing groups, such as chloro groups in aromatic rings in critical residues of various ligands, can have important steric or electronic effects resulting in significant changes in receptor affinity or selectivity (Jensen et al., 1985; Li et al., 1998; Perrone et al., 1998; Ananthan et al., 2003). As was seen in previous studies (Pradhan et al., 1998; Katsuno et al., 1999) [D-Tyr6,-Ala11,Phe13,Nle14]Bn(6-14) (Table 1, peptide 1) bound to all three human Bn receptor subtypes with high affinity (Fig. 2; Table 1). The replacement of the -Ala at position 11 by chloro-substituted 3-amino-3-phenylpropionic acid moieties (Fig. 2; Table 2, peptides 4-9) resulted in peptides that when compared with peptide 1, had from 10- to 800-fold less affinity for the hBRS-3 but in general had increased selectivity for the hBRS-3 because they became even less potent at the hGRP-R and the hNMB-R (Fig. 2; Table 1). In this group of six peptides, there were three sets of R- and S-optical isomers (Table 1, peptides 4 and 5, 6 and 7, 8 and 9; Fig. 2). The R-isomers showed more selectivity for hBRS-3 over hGRP-R and hNMB-R than the S-isomers. Except for [D-Tyr6,(S)-Apa11-4Cl,Phe13,Nle14]Bn(6-14) (Table 1, peptide 6), which was equipotent for hBRS-3 and hGRP-R, these peptides had from 5- to 800-fold increase in selectivity for the hBRS-3 over hGRP-R and from 3- to 900-fold increase in selectivity for hBRS-3 over hNMB-R (Fig. 2; Table 1) compared with the original -Ala11 analog (Table 1, peptide 1). The peptide that showed the highest selectivity for hBRS-3 over both hGRP-R and hNMB-R was [D-Tyr6,(R)-Apa11-4Cl,Phe13,Nle14]Bn(6-14) (Table 1, peptide 7), which, when compared with the original -Ala11 peptide (Table 1, peptide 1), was 10 times less potent for hBRS-3 (Ki = 8.2 ± 1.1 versus 0.82 ± 0.1 nM); however, it was 227- and 878-fold more selective for hBRS-3 than hGRP-R and hNMB-R, respectively (Fig. 2; Table 1). A 3-chloro-substitution on the (R)-Apa11 group yielding [D-Tyr6,(R)-Apa11-3Cl,Phe13,Nle14]Bn(6-14) resulted in a peptide (Fig. 2; Table 2, peptide 9) that was very selective for hBRS-3 but is unlikely to be useful, because of its low affinity for hBRS-3 (Ki = 107 ± 4 nM).
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Previous studies have shown that the substitution at position 14 can have a pronounced effect on a peptide ligand's affinity for GRP-R and NMB-R, in addition to the position 11 substitution (Saeed et al., 1989; Wang et al., 1990; Lin et al., 1996; Mantey et al., 1997, 2001). We therefore made six peptides with substitutions of different conformationally restricted amino acids of different sizes and polarity at positions 11 or 14 (Table 1; Fig. 3, peptides 10-15). This group of peptides consisted of a 2,3-diaminopropionic acid-proline substitution at position 14 (peptide 15) and five different substitutions at the -Ala in position 11 of [D-Tyr6,-Ala11,Phe13,Nle14]Bn(6-14) (Table 1; Fig. 3, peptides 9-14). These alterations produced peptides with a 3- to 3000-fold decrease in affinity for the hBRS-3 receptor compared with the prototype -Ala11 peptide (Table 1, peptide 1) and none demonstrated increased selectivity for hBRS-3 over hGRP-R and hNMB-R. In fact, in general these peptides became less selective for hBRS-3 and more selective for hGRP-R. Specifically, peptides 10 and 11 (Table 1; Fig. 3), which have a -COOH and benzylamide substitution, respectively, added at the position of -Ala11 (Fig. 1), showed a decrease in affinity (60-75-fold) to all the Bn receptor subtypes (Table 1; Fig. 3). The three peptides in this group with substitution at the position of the -Ala11 (Table 1, peptides 12-14; Figs. 1 and 3) had a 3- to 18-fold decrease in affinity (Ki = 2.3 ± 0.1, 15.8 ± 2.9, and 12.3 ± 1.3 nM, respectively) for the hBRS-3 receptor but retained high affinity for hGRP-R (Ki = 1.0 ± 0.1-3.1 ± 0.5 nM), making them hGRP-R-selective. The insertion of a substituted Dap moiety in position 14 (Table 1, peptide 15; Fig. 3) resulted in a peptide that had >20-fold selectivity for hGRP-R over hBRS-3 or hNMB-R.
Bn and NMB have very low affinities (Ki > 10,000) for the hBRS-3 (Table 1) compared with the ability of these peptides to interact with hGRP-R (Fig. 3, middle; Table 1) or with the hNMB-R (Fig. 3, bottom; Table 1). These results are consistent with results from previous studies (Fathi et al., 1993; Wu et al., 1996; Mantey et al., 1997, 2001; Pradhan et al., 1998; Ryan et al., 1998a) that show the hBRS-3 receptor is unique among the mammalian Bn receptor family because it interacts with all the naturally known Bn-related peptides with very low affinity.
In previous studies, it was reported that the nonselective prototype ligand [D-Tyr6,-Ala11,Phe13,Nle14]Bn(6-14) (Table 1, peptide 1), and the more hBRS-3-selective ligand [D-Tyr6,(R)-Apa11,Phe13,Nle14]Bn(6-14) (Table 1, peptide 2), specifically interact with the Bn family of receptors (Mantey et al., 1997, 2001). To determine whether the addition of a 4-chloro group to the Apa11 made the newly discovered hBRS-3-selective peptide [D-Tyr6,(R)-Apa11-4Cl,Phe13,Nle14]Bn(6-14) (Table 1, peptide 7) less selective for the Bn group of receptors, we investigated its ability to interact with a number of other receptors involved with the actions of gastrointestinal hormone/neurotransmitters (Table 2). Similar to the nonselective Bn analog peptide 1, the hBRS-3-selective analog peptide 7, at a concentration that completely inhibited binding to the hBRS-3 receptor (i.e., 1 µM) (Fig. 2), did not inhibit binding to receptors for cholecystokinin, gastrin, PACAP, VIP (VPAC1-R and VPAC2-R), somatostatin, muscarinic cholinergic agents, or substance P (Table 2). This lack of activity at these receptors was not due to the fact that either Bn analog is inactivated, because the assays were performed under the same conditions used to assess binding to Bn receptors, and in the different assays using the same cells, both peptides 1 and 7 inhibited binding to GRP receptors on rat pancreatic acini. These results demonstrate that the newly discovered selective peptide, peptide 7, has high selectivity for the Bn family of receptors.
The comparative abilities of the nonselective hBRS-3 ligand [D-Tyr6,-Ala11,Phe13,Nle14]Bn(6-14), the two hBRS-3-selective ligands from our previous study (Mantey et al., 2001) (Table 1, peptides 2 and 3), and the most selective hBRS-3 ligand found in the present study (Table 1, peptide 7) to interact with the three mammalian Bn receptor subtypes are shown in Fig. 4 and Table 1. Each of the three selective peptides retained high affinity for hBRS-3 receptor (nanomolar range), but were from 3- to 10-fold less potent than the nonselective prototype peptide (Table 1, peptide 1). However, each of these three hBRS-3 peptides became more hBRS-3-selective because their affinities for hGRP-R and hNMB-R were diminished substantially compared with peptide 1, the prototype peptide (Table 1; Fig. 4). Specifically, similar to what has been reported previously (Mantey et al., 2001), the R-isomer of Apa11, [D-Tyr6,(R)Apa11,Phe13,Nle14]Bn(6-14)] (Table 1, peptide 2) was more hBRS-3 receptor-selective than the S-isomer [D-Tyr6,(S)Apa11,Phe13,Nle14]Bn(6-14) (Table 1, peptide 3). The 4-chloro-substitution on the (R)-Apa11 (Table 1, peptide 7; Fig. 4) yielded a peptide that was significantly more selective for hBRS-3 over hGRP-R (227-fold over hGRP-R) compared with the hBRS-3 selectivity of peptide 2 described in a previous study (Mantey et al., 2001) (54-fold over hGRP-R). Both peptide 7 and peptide 2 (Table 2) were more than 800-fold selective for hBRS-3 over hNMB-R (Table 1; Fig. 4)
Activation of hBRS-3, hGRP-R, and hNMB-R results in the stimulation of phospholipase C activity with increases in inositol phosphates (Benya et al., 1992, 1994, 1995; Mantey et al., 2001). To assess whether the newly discovered hBRS-3 receptor-selective peptide [D-Tyr6,(R)-Apa11-4Cl,Phe13,Nle14]Bn(6-14) (Table 1, peptide 7) is an agonist at this receptor and whether its selectivity in binding to hBRS-3 is mirrored in its ability to activate the receptor, we determined its ability compared with those of peptides 1, 2, 3, Bn, and NMB to stimulate [3H]IP release in cells transfected with hBRS-3, hGRP-R, and hNMB-R (Table 3; Fig. 5). All peptides stimulated increases in [3H]IP in a concentration-dependent manner at each of the three Bn receptor subtypes (Fig. 5). At a concentration of up to 10 µM, each peptide functioned as a full agonist (Fig. 5). The nonselective peptide (Table 1, peptide 1) [D-Tyr6,-Ala11,Phe13,Nle14]Bn(6-14) stimulated increases in [3H]IP in hBRS-3, hGRP-R, and hNMB-R with high potencies (EC50 = 0.17-1 nM) (Table 3; Fig. 5). Both Bn and NMB had very low potencies for stimulation at the hBRS-3. NMB had a high potency for activating hNMB-R (EC50 = 1.2 ± 0.1) but lower potency for the hGRP-R (EC50 = 530 ± 23), whereas Bn had a high potency for stimulating both hGRP-R and hNMB-R (0.4 ± 0.06 and 2.5 ± 0.1, respectively). Similar to previous results (Mantey et al., 2001), peptides 2 and 3, which are Apa11-substituted compounds (Table 1), had 
6-fold selectivity for activating hBRS-3 over hGRP-R and hNMB-R. The most selective hBRS-3 receptor ligand identified in the present study, peptide 7, [D-Tyr6,(R)-Apa11-4Cl,Phe13,Nle14]Bn(6-14), had >20-fold selectivity for activating the hBRS-3 receptor over hGRP-R or hNMB-R. Therefore, peptide 7 was 10- and 4-fold more selective for activating the hBRS-3 receptor over the hGRP-R and hNMB-R, respectively, than peptide 2, [D-Tyr6,(R)-Apa11,Phe13,Nle14]Bn(6-14), the most hBRS-3-selective peptide described previously (Mantey et al., 2001).
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Discussion |
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TopAbstractMaterials and MethodsResultsDiscussionReferences |
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; Ryan et al., 1998a,1998b), we reported the discovery of a synthetic analog of Bn, [D-Tyr6,-Ala11,Phe13,Nle14]Bn(6-14), which functioned as a potent agonist for the human G protein-coupled orphan receptor BRS-3, a receptor that is structurally related to mammalian Bn receptors (Fathi et al., 1993; Gorbulev et al., 1994). In subsequent studies (Pradhan et al., 1998; Reubi et al., 2002), this Bn analog was also found to have the unique property of having high affinity for all known mammalian Bn receptors (i.e., GRP-R and NMB-R), as well as the amphibian Bn receptor bombesin receptor subtype 4 (Nagalla et al., 1995; Katsuno et al., 1999), except for the BRS-3 receptor in rat and mouse (Liu et al., 2002). Whereas this finding made this Bn analog valuable as a universal ligand for identifying Bn receptor subtypes (Pradhan et al., 1998; Reubi et al., 2002), its lack of selectivity for the BRS-3 receptor decreased its usefulness for investigating the role of hBRS-3 only in physiological or pathological processes. In previous studies, none of the naturally occurring Bn-related peptides, nor more than 30 synthetic Bn analogs interacted with high affinity or selectivity with the hBRS-3 receptor (Fathi et al., 1993; Wu et al., 1996; Mantey et al., 1997, 2001; Ryan et al., 1998a,b; Katsuno et al., 1999; Liu et al., 2002). However, in a recent study (Mantey et al., 2001) investigating replacement of -Ala11 of the nonselective high-affinity hBRS-3 ligand, [D-Tyr6,-Ala11,Phe13,Nle14]Bn(6-14), with conformationally restricted amino acids, two peptides with an (R)- or (S)-Apa substitution for -Ala11 were reported with some selectivity for the hBRS-3 receptor. However, this selectivity was relatively modest for their differential potencies for receptor activation of hBRS and the Bn receptors hGRP-R and hNMB-R, because of different degrees of receptor spareness in these different receptors (Mantey et al., 2001). Specifically in the present study, the (R)-Apa11 and (S)-Apa11 analogs had 50- and 13-fold selectivity for the hBRS-3 over the hGRP-R or hNMB-R by binding studies, but only a 7- and 3-fold selectivity in potency for activating hBRS-3 over the hGRP-R and hNMB-R, and for stimulating phospholipase C activity. The aim of the present study was to attempt to identify additional synthetic Bn analogs with enhanced hBRS-3 selectivity.
Two strategies were used to attempt to identify more selective hBRS-3 receptor ligands. The first strategy involved inserting additional substitutions on the phenyl ring of Apa in position 11 of the R- and S-isomers of the selective hBRS ligand [D-Tyr6,Apa11,Phe13,Nle14]Bn(6-14), which might change either its steric or electronic properties. This strategy was taken because molecular modeling studies (Mantey et al., 2001) using a -bend template, a conformation that has been proposed for the Val10-Gly11-His12-Phe13 COOH terminal region of Bn (Coy et al., 1991; Mantey et al., 2001), demonstrated these two hBRS-3-selective Bn analogs had a unique orientation of the position 11 -amino acid that likely contributed to their selectivity for BRS-3. Therefore, further alteration of the conformation might enhance hBRS-3 selectivity. The second approach was to substitute additional conformationally restricted amino acids in the place of Apa at primarily position 11. Because of the previous molecular modeling results (Mantey et al., 2001), which suggested the importance of orientation of the backbone substitution of the conformationally restricted amino acid in position 11, suggesting steric factors were important in determining hBRS-3 selectivity, chloro substitutions were made on 2, 3, and 4 positions of the phenyl ring of Apa11 in the R- and S-isomers. Previous studies on ligands for the CCK receptor (Jensen et al., 1985), A3 adenosine receptor (Li et al., 1998), D4 dopamine receptor (Perrone et al., 1998), and opioid receptors (Ananthan et al., 2003) have demonstrated that insertion of electron-withdrawing groups such as chloro substitutions in the phenyl ring can have important effects on receptor selectivity and affinity by either altering steric or electronic properties of the ligand. Our results demonstrate that the insertion of a chloro group in the ortho, meta, or para position of the phenyl ring in relation to the Apa group had a markedly different effect on the Bn receptor selectivity. Furthermore, the effect of the chloro insertion in the different phenyl ring positions had markedly differing effects on the absolute and relative potencies of Apa11 Bn analog containing either the (R)- or (S)-Apa isomer. The latter result might be expected from the molecular modeling result (Mantey et al., 2001) reported earlier if the insertion of the chloro group was having primarily a steric effect, because in these models the (R)- and (S)-Apa11 analogs had a unique conformation that differed from the other constrained position 11 analogs tested; however, their conformations were not identical; therefore, insertion of a steric group in the different phenyl ring position could have a differing effect. Of the different chloro Apa11 analogs tested, the insertion of the chloro in the para position of the phenyl ring in the (R)Apa11 analog resulted in an analog that had significantly improved selectivity for hBRS-3 and that retained sufficiently high affinity for hBRS-3 to be likely useful to explore these receptors' roles in various processes. Specifically, [D-Tyr6,(R)-Apa11-4Cl,Phe13,Nle14]Bn(6-14) had a 227- and 880-fold selectivity for hBRS-3 over hGRP-R and hNMB-R by binding studies, and a 90- and 20-fold greater potency for activating the hBRS-3, respectively. Therefore, the four chloro Apa11 analog has 20- and 5-fold greater selectivity for the hBRS-3 over the hGRP-R by binding studies than the previously reported selective (S)- and (R)-Apa11 analogs (Mantey et al., 2001). Furthermore, in terms of relative potencies for activating hBRS-3 and the two Bn receptor subtypes, the 4 chloro (R)-Apa11 analog had 10- and 4-fold greater selectivity than the previously reported selective (S)- and (R)-Apa11 analogs (Mantey et al., 2001). In a previous study (Mantey et al., 2001), replacement of the phenyl ring of the Apa11 analog with an (R)-4 chlorobenzyl group resulted in a Bn analog (Acpb4, compound VIII; Mantey et al., 2001) with a 100-fold less affinity for hBRS-3 and almost no selectivity for hBRS-3 over hGRP-R (3-fold) or hNMB-R (9-fold) (Mantey et al., 2001). These findings, in comparison with the present results with the 4 chloro-phenyl substitution in Ala11 resulting in retained high affinity for hBRS-3 and increased selectivity, demonstrate the importance of the size of the substitution in the aminopropionic acid in position 11 for determining both affinity and selectivity.
Whereas the first strategy of insertion of chloro groups on the Apa11 phenyl ring of [D-Tyr6,(R)-Apa11,Phe13,Nle14]Bn(6-14) resulted in one potentially useful compound with enhanced BRS-3 selectivity, the second strategy of substitution of other conformationally restricted amino acids for Apa11 or in position 14 for Nle, did not result in any Bn analogs with enhanced hBRS-3 selectivity. The results using this strategy did, however, provide some interesting insights into the importance of backbone substitutions on the aminopropionic acid moiety in the 11 position of the [D-Tyr6,-Ala11,Phe13,Nle14]Bn(6-14) that are important in determining receptor selectivity and/or affinity. In a previous study (Mantey et al., 2001), the effect of various aliphatic and aromatic substitutions at the and position of aminopropionic acid in [D-Tyr6,Apa11,Phe13,Nle14]Bn(6-14) were investigated and shown to have a marked effect on affinity and selectivity for hBRS-3, hGRP-R, and hNMB-R. In the present study, the effect of forming a carboxylic acid, an amine or amide with these substitutions on Apa in position 11 was investigated. The formation of aspartic acid by insertion of a -carboxyl group with or without a benzilamide group markedly decreased affinity for all human Bn receptor subtypes. In contrast, amino or various amide substitutions in the position, even of different sizes, were well tolerated in contrast to the position of Apa where backbone size was a critical factor (Mantey et al., 2001). Unfortunately, substitutions in the position of Apa11 do not seem to be important for hBRS or Bn receptor selectivity.
In conclusion, using stereospecific substitutions of chloro groups in the hBRS-3-preferring ligands, [D-Tyr6,(R)- or (S)Apa11,Phe13,Nle14]Bn(6-14), one peptide was identified with enhanced selectivity for the hBRS-3 over the hGRP-R or hNMB-R. The availability of this analog as well as the recently described (Weber et al., 2002, 2003) short bombesin peptide agonists identified from systematic optimization of [D-Phe6,-Ala11,Phe13,Nle14]Bn(6-14), which have high selectivity for the hBRS-3, could be useful for investigating the possible role of hBRS-3 in various physiological or pathological processes.
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ABBREVIATIONS: BRS-3, bombesin receptor subtype 3; Bn, bombesin; GRP, gastrin-releasing peptide; GRP-R, gastrin-releasing peptide receptor; NMB, neuromedin B; NMB-R, neuromedin B peptide receptor; FBS, fetal bovine serum; CCK, cholecystokinin; VIP, vasoactive intestinal peptide; PACAP, pituitary adenylate cyclase-activating peptide; Apa, aminopropionic acid; -Ala, -alanine; -Asp, Boc--aspartic acid; Cl, chloro; -AspBzlAmd, Boc--aspartic acid benzilamide; N-acetyl-Dap, 2-acetylamino,3-aminopropionic acid; N-benzoyl-Dap, 2-benzoylamino,3-aminopropionic acid; -Dap, 2,3,diaminopropionic acid; -Dap(Pr), 2,3-diaminopropionic acid-proline; Acpb4-Boc(R)-3-amino-3-(4-chlorobenzyl)-propionic acid; hBRS-3, human bombesin receptor subtype 3; CHO, Chinese hamster ovary; IP, inositol phosphates; Nle, norleucine.
Address correspondence to: Dr. Robert T. Jensen, Digestive Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bldg. 10, Room 9C-103, 10 Center Dr., MSC 1804, Bethesda, MD 20892-1804. E-mail: robertj{at}bdg10.niddk.nih.gov
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