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Open Access

AChBP‐targeted α‐conotoxin correlates distinct binding orientations with nAChR subtype selectivity

Sébastien Dutertre, Chris Ulens, Regina Büttner, Alexander Fish, René van Elk, Yvonne Kendel, Gene Hopping, Paul F Alewood, Christina Schroeder, Annette Nicke, August B Smit, Titia K Sixma, Richard J Lewis

Author Affiliations

  1. Sébastien Dutertre1,,
  2. Chris Ulens2,,
  3. Regina Büttner3,
  4. Alexander Fish2,
  5. René van Elk4,
  6. Yvonne Kendel5,
  7. Gene Hopping1,
  8. Paul F Alewood1,
  9. Christina Schroeder1,
  10. Annette Nicke3,
  11. August B Smit4,
  12. Titia K Sixma*,2 and
  13. Richard J Lewis*,1
  1. 1 Institute for Molecular Bioscience, The University of Queensland, Brisbane, Queensland, Australia
  2. 2 Division of Molecular Carcinogenesis and Center for Biomedical Genetics, Netherlands Cancer Institute, Plesmanlaan, CX Amsterdam, The Netherlands
  3. 3 Department of Neurochemistry, Max Planck Institute for Brain Research, Deutschordenstrasse 46, Frankfurt am Main, Germany
  4. 4 Department of Molecular and Cellular Neurobiology, Center for Neurogenomics and Cognitive Research, Vrije Universiteit, Amsterdam, The Netherlands
  5. 5 Zentrum der Rechtsmedizin, University of Frankfurt, Frankfurt am Main, Germany
  1. *Corresponding authors: Institute for Molecular Bioscience, The University of Queensland, Carmodty Rd, Brisbane, Queensland 4072, Australia. Tel.: +617 3346 2984; Fax: +617 3346 2101; E-mail: r.lewis{at}imb.uq.edu.au Division of Molecular Carcinogenesis and Center for Biomedical Genetics, Netherlands Cancer Institute, Plesmanlaan, 1066 CX Amsterdam, The Netherlands. E-mail: t.sixma{at}nki.nl
  1. These authors contributed equally to this work

  • Present address: Max Planck Institute for Brain Research, Deutschordenstrasse 46, 60528 Frankfurt am Main, Germany.

Abstract

Neuronal nAChRs are a diverse family of pentameric ion channels with wide distribution throughout cells of the nervous and immune systems. However, the role of specific subtypes in normal and pathological states remains poorly understood due to the lack of selective probes. Here, we used a binding assay based on acetylcholine‐binding protein (AChBP), a homolog of the nicotinic acetylcholine ligand‐binding domain, to discover a novel α‐conotoxin (α‐TxIA) in the venom of Conus textile. α‐TxIA bound with high affinity to AChBPs from different species and selectively targeted the α3β2 nAChR subtype. A co‐crystal structure of Ac‐AChBP with the enhanced potency analog TxIA(A10L), revealed a 20° backbone tilt compared to other AChBP–conotoxin complexes. This reorientation was coordinated by a key salt bridge formed between Arg5 (TxIA) and Asp195 (Ac‐AChBP). Mutagenesis studies, biochemical assays and electrophysiological recordings directly correlated the interactions observed in the co‐crystal structure to binding affinity at AChBP and different nAChR subtypes. Together, these results establish a new pharmacophore for the design of novel subtype‐selective ligands with therapeutic potential in nAChR‐related diseases.

Introduction

Acetylcholine binding proteins (AChBPs) have been identified from different snails, including Lymnaea stagnalis (Smit et al, 2001), Aplysia californica (Hansen et al, 2004; Celie et al, 2005a) and Bulinus truncatus (Celie et al, 2005b). AChBPs are homologous to the ligand‐binding domains (LBDs) of the nicotinic acetylcholine receptors (nAChRs) and pharmacological characterization has demonstrated that their properties most closely resemble those of the α7 nAChRs (Smit et al, 2001), which also function as homopentamers. Crystallization and structure determination of AChBPs (Hansen et al, 2005; Celie et al, 2005a, 2005b) from these different species has revealed a highly conserved architecture, despite the relatively low sequence identity between different AChBPs. A similar level of sequence homology is found with the LBDs of members of the ligand‐gated ion channel family, comprising the nAChRs, GABA‐A/C receptors, 5‐HT3 and glycine receptors. AChBP has been co‐crystallized with prototype ligands that are known to bind to nAChRs, thus establishing the structural determinants for ligand recognition of agonists such as nicotine and carbamylcholine (Celie et al, 2004), and antagonists such as different α‐conotoxins (Celie et al, 2005a; Ulens et al, 2006) and long‐chain snake neurotoxins (Bourne et al, 2005), and partial agonists such as lobeline (Hansen et al, 2005). Comparison of these different crystal structures has revealed conformational changes occurring upon ligand binding, and has allowed predictions as to how these conformational changes may be coupled to channel opening through the loops that form the interface with the transmembrane domain in the nAChR.

The venoms from cone snails are a rich source of peptides with high affinity for several voltage‐ and ligand‐gated ion channels, including nAChRs (Olivera et al, 1990). Recently, we and others have solved crystal structures of Ac‐AChBP in complex with two different α‐conotoxins, namely PnIA(A10L D14K) (Celie et al, 2005a) and ImI (Hansen et al, 2005; Ulens et al, 2006). These two conotoxins greatly differ in their selectivity among AChBPs and comparison of the toxin–receptor interface in both complexes provided structural insight into the molecular determinants of ligand selectivity (Ulens et al, 2006).

In addition to being remarkable probes for structural studies, α‐conotoxins also have therapeutic potential (Lewis and Garcia, 2003). For example, Vc1.1, the first α‐conotoxin being developed to treat neuropathic pain also caused an accelerated recovery of injured neurons (Satkunanathan et al, 2005). Recently, Vc1.1 was shown to specifically target α910 nAChRs, providing a rationale for its analgesic property (Vincler et al, 2006). Determining the specific roles of the multiple nAChR subtypes under physiological or pathological conditions and the development of drugs to treat nAChR‐related disorders, such as Parkinson's disease and nicotine addiction, requires further subtype‐selective ligands.

In this study, we used Ls‐AChBP as a bait to discover the novel α‐conotoxin TxIA from Conus textile. Pharmacological characterization shows that TxIA binds with very high affinity to AChBPs from different species, as well as selectively to certain subtypes of neuronal nAChRs. The co‐crystal structure of Ac‐AChBP with a more potent analog TxIA(A10L), revealed that this α‐conotoxin adopts a different binding orientation to that observed for other α‐conotoxin–AChBP complexes. A salt bridge between Arg5 in TxIA(A10L) and Asp195 of Ac‐AChBP was visible in the structure and the importance of this interaction for AChBP binding and nAChR selectivity was established using binding assays, surface plasmon resonance (SPR) and electrophysiological experiments with mutant receptors and conotoxin analogs. These results highlight the potential of an AChBP screen to discover novel ligands acting at the nAChR and provide a new pharmacophore for the design of ligands with improved subtype selectivity.

Results

Identification and pharmacological characterization of α‐conotoxin TxIA

We tested the activity of crude venoms obtained from more than 30 species of Australian cone snails against Ls‐AChBP in a competitive binding assay with radiolabeled α‐bungarotoxin (125I‐Bgt). We chose the venom of cone snails as our ‘combinatorial library of ligands’, as all species tested so far were shown to contain at least one nAChR ligand among the 50–200 unique conopeptides known to occur in each venom (McIntosh et al, 1999). Accordingly, the venoms from all species showed some competition in our Ls‐AChBP‐binding assay (Figure 1A). We focused on C. textile venom, as full competition with 125I‐Bgt was observed, indicating the presence of a high affinity or abundant ligand (Figure 1A). Upon isolation the active compound was found to be in low abundance, indicating that it was relatively potent (Figure 1B). Mass spectrometry revealed a monoisotopic mass of 1656.68 Da, similar in size to previously isolated α‐conotoxins. N‐terminal sequencing revealed a novel 16 amino‐acid peptide belonging to the 4/7 α‐conotoxin family, which we named α‐conotoxin TxIA (Table I). The calculated mass (1661.67 Da) was consistent with two disulfide bonds (–4 Da) and an amidated C terminus (–1 Da), two post‐translational modifications common in this class of conotoxins (Loughnan and Alewood, 2004).

Figure 1.

Isolation and characterization of α‐conotoxin TxIA. (A) Ls‐AChBP screening for α‐conotoxins in venoms of 30 species of Australian cone snails. (B) LC‐MS profile of the crude venom of C. textile. TxIA was isolated as a minor component shown in the extracted ions for this peptide. Inset shows a shell of C. textile. (C) Saturation binding experiments revealed a competitive interaction of TxIA with Ls‐AChBP. When an ∼IC50 concentration of TxIA was added, the Kd of 125I‐Bgt shifted from 3.5 to 40 nM, whereas the Bmax remained unaffected. (D) Displacement of 125I‐Bgt from Ls‐AChBP by α‐conotoxins TxIA, PnIA and analogs (plot with all fixed to 100% in curve fit). Data in (A), (C) and (D) represent the mean±s.e.m. of duplicate data obtained in three separate experiments.

View this table:
Table 1. Binding affinities (nM) of α‐conotoxins for Ls‐AChBP

Synthetic analogs of TxIA were assembled using Boc chemistry for further analysis and to determine the cysteine connectivity. The ‘native’ conformation (connectivity 1–3, 2–4) and the ‘ribbon’ fold (connectivity 1–4, 2–3) were both able to displace 125I‐Bgt bound to Ls‐AChBP. However, whereas the native fold displayed a Ki of 1.7 nM, the ribbon fold was 380‐fold less potent (Supplementary Figure 1). Therefore, the connectivity is assumed to be 1–3, 2–4 in the venom‐isolated α‐TxIA, as was found in all other α‐conotoxins identified to date. Comparison with other synthetic α‐conotoxins known to bind nAChRs revealed that α‐TxIA is 50‐fold more potent than the α7 nAChR‐selective PnIA(A10L) in displacing 125I‐Bgt at Ls‐AChBP (Table I). The muscle nAChR‐selective EI displayed an intermediate Ki value of 496 nM, followed in decreasing order of potency by the α3β2 nAChR‐selective PnIA (1.0 μM) and the α63β2 nAChR‐selective MII (1.1 μM), whereas EpI had the lowest affinity (7 μM). Previously, pH was shown to influence the potency of the histidine‐containing α‐MII in functional assays (Everhart et al, 2004). This effect also applies to MII binding to Ls‐AChBP (Spearman's test, P<0.01), whereas the other toxins were most active at physiological pH (Supplementary Figure 2). In a saturation‐binding experiment, addition of an ∼IC50 concentration of native α‐TxIA increased the Kd of 125I‐Bgt from 3.5 to 40 nM without affecting the maximum binding Bmax, indicative of a competitive binding interaction (Figure 1C). α‐TxIA was also tested on rat brain membranes using 125I‐Bgt and 3H‐epibatidine as tracers to determine the affinity for α7 and mostly α4β2 neuronal nAChRs, respectively. α‐TxIA displaced 125I‐Bgt with a Ki of 1.2 μM (α7 nAChR), but failed to displace 3H‐epibatidine using up to 10 μM of peptide. Finally, α‐TxIA was tested in a functional assay on heterologously expressed mammalian nAChRs (Figure 2). α‐TxIA potently inhibited nicotine‐induced current at the α3β2 nAChR (IC50=3.5 nM) and α7 nAChRs (IC50=392 nM), but had no activity at the α4β2 nAChR and muscle nAChR at concentrations up to 10 μM. Thus, α‐TxIA is among the most α3β2‐selective toxins identified.

Figure 2.

Antagonist activity of α‐conotoxin TxIA and analogs at oocyte‐expressed rat α3β2 (A) and α7 (B) nAChRs. Oocytes were clamped at −70 mV and 100 μM ACh (α3β2) or nicotine (α7) were applied for 2 s in 4 min intervals. Toxins were applied for 3 min. Data are represented as the mean±s.e.m. of at least four oocytes.

Structure activity relationships

The sequence of α‐TxIA was compared to previously identified 4/7 α‐conotoxins (Table I). Interestingly, only three residues are different from α‐conotoxin PnIA, yet PnIA is 600‐fold less potent than TxIA at Ls‐AChBP. To identify which of these residues conferred the high affinity at Ls‐AChBP, we synthesized PnIA and TxIA mutants covering two of the three differences (Figure 1D and Table II). A third difference at position 15 was not investigated, as it was located outside the binding site identified in the co‐crystal structure of Ac‐AChBP with PnIA(A10L D14K) (Celie et al, 2005a). For the mutants tested, PnIA(A10L) had 12.5‐fold higher affinity at Ls‐AChBP, 20‐fold higher affinity at the α7 nAChR, but 10‐fold reduced affinity at the α3β2 nAChR (Hogg et al, 1999; Luo et al, 1999; Dutertre et al, 2005) (Table II). In contrast, TxIA(A10L) had similar potency to native TxIA at Ls‐AChBP (Figure 1D and Table II), suggesting that Ile9 (Ala in PnIA) is able to substitute for Leu10 in PnIA(A10L) in the conserved hydrophobic patch that we have shown previously interacts with the complementary binding site of the nAChR (Dutertre et al, 2005). Despite the lack of effect on Ls‐AChBP affinity, TxIA(A10L) was 12‐ and 2‐fold more potent at the α7 and α3β2 nAChRs, respectively (Figure 2). Thus, a long‐chain hydrophobic residue (Leu or Ile) at position 9 or 10 is important for high‐affinity binding of TxIA and PnIA to Ls‐AChBP and the α7 nAChRs, but not α3β2 nAChRs. A second difference is a Leu in position 5 of PnIA compared with an Arg in TxIA. As this position is well placed to directly interact with the receptor (Dutertre et al, 2005), this change in the physical property and length of the side chain could be an important contributor to high‐affinity binding to Ls‐AChBP. In support of this hypothesis, EI also has high affinity for Ls‐AChBP and a positive charge in the equivalent position, whereas the low affinity [Y15]‐EpI has a negatively charged aspartic acid at this position. In agreement with these observations, PnIA(L5R A10L) had 220‐fold increased affinity for Ls‐AChBP compared to PnIA, clearly demonstrating the important role of Arg5 for high‐affinity binding to Ls‐AChBP (Figure 1D and Table II). The role of this residue appears also important for α3β2 nAChR binding (10‐fold increased affinity of PnIA(L5R A10L) compared to PnIA(A10L) at α3β2 nAChR), but not for the α7 nAChR (same affinity compared to PnIA(A10L)), suggesting that Arg5 interacts with Ls‐AChBP and α3β2 nAChRs in a similar manner (Figure 2 and Table II).

View this table:
Table 2. Potency (nM) of α‐conotoxins TxIA, PnIA and analogues at AChBP and rat nAChRs

Crystal structure of Ac‐AChBP in complex with TxIA(A10L)

To gain further insight into the nature of the interactions of α‐TxIA with AChBP and their contribution to high affinity binding, we solved the crystal structure of Ac‐AChBP in complex with the most potent TxIA analog, TxIA(A10L). Co‐crystals were initially obtained with Ls‐AChBP, Bt‐AChBP and Ac‐AChBP, but the latter gave diffraction data of better quality (see Supplementary Table I for statistics). TxIA(A10L) has comparable affinities to displace 3H‐epibatidine from Lymnaea and Aplysia AChBPs (data not shown). The structure of the complex was determined at 2.4 Å resolution (Figure 3A) and solved by molecular replacement. The asymmetric unit contains two pentamers and all binding sites were occupied by TxIA(A10L). The structure of Ac‐AChBP in complex with TxIA(A10L) is very similar to other α‐conotoxin complexes, with r.m.s.d. of 0.73 Å (1023 Cα atoms) upon superposition with the complex of Ac‐AChBP with PnIA(A10L D14K) (Celie et al, 2005a) and 0.67 Å (1024 Cα atoms) for the Ac‐AChBP complex with ImI (Ulens et al, 2006). The r.m.s.d. between monomers in the Ac‐AChBP–TxIA(A10L) complex is 0.34±0.04 Å. TxIA(A10L) binds with loop C displaced outward by a distance of 10.87±0.50 Å as measured between the Cys188 Cα atom in the Ac‐AChBP complex with TxIA(A10L) and the HEPES‐bound Ac‐AChBP structure (Celie et al, 2005a), similar to values measured for other α‐conotoxin complexes. We previously observed ∼3° rigid body rotations of the monomers in the Ac‐AChBP complex with PnIA(A10L D14K) (Celie et al, 2005a), whereas these rotations were not seen in the Ac‐AChBP complex with ImI (Ulens et al, 2006). The Ac‐AChBP complex with TxIA(A10L) displays intermediate rotations (1–2°) of the monomers with respect to each other, which are most likely due to crystal contacts. The structure of TxIA(A10L) itself is very similar to other α‐conotoxins and has an r.m.s.d. of 0.64±0.10 Å upon superposition with PnIA (PDB accession code 1PEN). TxIA(A10L) covers a surface area in the binding pocket of 788±18 Å2, which is intermediate between the receptor–toxin interfaces formed with PnIA(A10L D14K) (827±32 Å2) and ImI (679±15 Å2) (Ulens et al, 2006).

Figure 3.

(A) Crystal structure of Ac‐AChBP in complex with TxIA(A10L). The model is shown along the five‐fold symmetry axis. α‐Conotoxins are shown in red. (B) Superposition of the subunit interface from Ac‐AChBP in complex with TxIA(A10L) and PnIA(A10L D14K). The principal face of the binding site is shown in shades of yellow, the complementary face in shades of blue. The superposition illustrates the different orientation of the conotoxin backbone in the binding pocket. PnIA(A10L D14K) is shown in blue, TxIA(A10L) in red. (C) Comparison of the different backbone orientations observed in co‐crystal structures of Ac‐AChBP with different α‐conotoxins. TxIA(A10L), shown in red, is tilted by a 20° rotation around Pro7 with respect to PnIA(A10L D14K), shown in blue. The backbone orientation of α‐conotoxin ImI, shown in magenta, is very similar to PnIA(A10L D14K) even though it is much shorter and forms a different network of interactions. Lines represent disulfide bridges. Detailed view of the molecular interactions that results in the different backbone orientations of (D) TxIA, (E) PhIA(A10L D14K) and (F) ImI within the binding site. The principal face of the binding site is shown in yellow, the complementary face in blue. The conotoxins are colored according to the color scheme in (C). Dashed lines represent hydrogen bonds or electrostatic interactions.

We previously observed that PnIA(A10L D14K) and ImI share a similar orientation in the binding pocket, but differ dramatically in the nature of interactions formed within the binding site (Celie et al, 2005a; Ulens et al, 2006). Surprisingly, we see that TxIA(A10L) adopts an orientation that is different from those seen in other α‐conotoxin–AChBP complexes. TxIA(A10L) is tilted 20° downward by a pivotal reorientation of the conotoxin around Pro7 (Figure 3B), which results in displacement by a distance of 4.72±0.83 Å, as measured between the Cα atoms at position 14 in the TxIA(A10L) and PnIA(A10L D14K) complexes. This different orientation of the conotoxin compared to those seen in other complexes (Figure 3C) is sustained by Arg5, which projects deep onto the principal face of the binding site and forms a hydrogen bond with Tyr186 and a salt bridge with Asp195 (Figure 3D), an interaction not seen in any of the other α‐conotoxin complexes (Figure 3E and F). The structural data thus confirm a key role of Arg5 in the high‐affinity binding of TxIA(A10L) to Ac‐AChBP. The interface of TxIA(A10L) with the principal binding site is further characterized by the formation of four additional hydrogen bonds between TxIA and Pro7‐Trp145 (loop B), TxIA and Asn12‐Glu191 (loop C), and TxIA Pro7 and Asn11‐Tyr193 (loop C) (Figure 3D). TxIA Pro7 also seems to play a dominant role in forming extensive van der Waals interactions with residues of the principal face that are not involved in contacts with PnIA(A10L D14K), namely Tyr91 (loop A), and Ser144, Trp145, Val146 and Tyr147 (loop B). In contrast, interaction of TxIA(A10L) with residues of the complementary face are similar to those seen in the Ac‐AChBP complex with PnIA(A10L D14K) and are mostly hydrophobic in nature.

Comparison of the different AChBP–conotoxin complexes reinforces the notion that α‐conotoxins can use different surface contacts to interact with the principal binding site (Figure 4A), whereas the surface area that contacts the complementary face of the binding site remains relatively conserved (Figure 4B). The calculated surface area of conotoxin ImI (1221±13 Å2), for example, is smaller than PnIA(A10L D14K) (1508±17 Å2) and TxIA(A10L) (1488±29 Å2), but they all share a hydrophobic patch on one face of their surface that projects on the complementary binding site. On the other hand, ImI has two arginine residues (Arg7 and Arg11) that protrude into the principal binding site, a surface property not present in PnIA(A10L D14K). TxIA(A10L) seems to have surface properties that are intermediate between ImI and PnIA(A10L D14K), even though TxIA and PnIA are the same length and TxIA has the relatively exposed Arg5.

Figure 4.

Surface representation of the three α‐conotoxins that have been co‐crystallized with Ac‐AChBP. The surface of the α‐conotoxin facing the principal binding site is shown in (A), the complementary binding site in (B). Ac‐AChBP is shown in a transparent view for clarity. The principal subunit (+) of Ac‐AChBP is shown in yellow, the complementary subunit (−) in blue.

Functional importance of an electrostatic interaction for high affinity binding of α‐conotoxins to AChBPs and α3β2 nAChRs

Structure–activity relationships between TxIA analogs indicated an important role for Arg5 in the high‐affinity binding of TxIA to AChBPs. Indeed, incorporation of an Arg residue in PnIA(A10L) at the equivalent position enhanced the affinity for Ls‐AChBP that approached TxIA(A10L) affinity, with the tight electrostatic interaction between Arg5 of TxIA(A10L) and Asp195 of Ac‐AChBP seen in our co‐crystal structure explaining this effect. To further confirm this interaction, we mutated Asp195 in Ac‐AChBP to Ala, Asn and Lys (unfortunately, insufficient Ac‐AChBP D195K was expressed to allow a complete pharmacological characterization). In a competition assay, D195A and D195N showed binding properties for nicotine and acetylcholine that are comparable to wt Ac‐AChBP (Ki nicotine=0.68±0.10 μM and 0.81±0.13 μM for D195A and D195N, respectively). However, TxIA and TxIA(A10L) showed a 30‐ to 50‐fold reduction in affinity for the D195A and D195N mutants (Figure 5A). A similar reduction was also observed for PnIA(L5R A10L). In contrast, the affinity of PnIA(A10L D14K), which lacks an Arg at position 5, for D195A and D195N remained virtually unchanged. In addition, we compared the kinetic behavior of TxIA analogs on Ac‐AChBP and the D195A mutant using SPR. In agreement with results from the binding assay, we observe an approximately sixfold acceleration in the dissociation rate for Arg5‐containing α‐conotoxins TxIA, TxIA(A10L) and PnIA(L5R A10L), whereas the dissociation kinetics for PnIA(A10L D14K) were unaffected by the D195A mutation (Figure 5B). These results provide strong evidence that the observed drop in affinity for Arg5‐containing analogs at D195A can be directly attributed to the loss of an energetically favorable interaction with Asp195, which stabilizes Arg5‐containing α‐conotoxins in their bound position.

Figure 5.

Functional contribution of the electrostatic interaction between Arg5‐TxIA and an Asp residue of the principal binding subunit of Ac‐AChBP and different nAChR subtypes. (A) Ki estimates from binding assays on wild‐type Ac‐AChBP, D195A and D195N mutants demonstrating the loss of affinity for Arg5‐containing conotoxins. (B) Surface plasmon resonance experiments on wild‐type Ac‐AChBP (red traces) and D195A mutant (blue traces) for TxIA analogs and PnIA(A10L D14K). (C) Effect of the Asp‐mutations on the potency of TxIA and analogs to inhibit α7 and α3β2 nAChR current. (D, E) Homology models for the interaction of TxIA(A10L) with α3β2 and α7 nAChRs. The α3β2 model also shows the Arg–Asp interaction observed in the co‐crystal structure.

To extrapolate the functional importance of this electrostatic interaction to mammalian nAChRs, we introduced the equivalent D197A and D195A mutations in α3β2 and α7 nAChRs, respectively, and compared the potency of TxIA analogs by two‐electrode voltage clamp analysis on the oocyte expressed mutant receptors (Figure 5C). In agreement with the results obtained with the Ac‐AChBP mutants, we see that Arg5‐containing conotoxins had 200‐ to 500‐fold decreased activity at D197A‐α3β2. Together, these results show that the electrostatic interaction between Arg5 of TxIA(A10L) and Asp195 in Ac‐AChBP and Asp197 in α3β2 nAChRs provides an important energetic contribution to their enhanced affinity at these receptors. In contrast, the activities of TxIA, TxIA(A10L) and PnIA(L5R A10L) at D195A‐α7 were little affected, suggesting that other interactions, probably involving a the hydrophobic patch around position 9/10, dominate α‐conotoxin interactions with this subtype.

Comparison between nAChR subtypes

It was an intriguing finding that D195A and D197A mutations had a dramatic effect on TxIA binding at AChBP and α3β2 nAChR, respectively, whereas the corresponding mutation (D195A) in α7 nAChR barely affected the binding of Arg5‐containing conotoxins including TxIA. To help understand this difference, we constructed homology models of both nAChRs and docked TxIA(A10L) into its binding site. Analysis of conotoxin binding in the α3β2 receptor clearly shows that TxIA(A10L) adopts a backbone orientation that is similar to the binding mode observed in our Ac‐AChBP co‐crystal structure (Figure 5D). This interaction specifically allows an electrostatic interaction between Arg5 and the conserved Asp residue D197, in agreement with our experimental results. To further confirm the existence of this novel binding mode in native α3β2 nAChRs, we utilized a β2‐subunit mutant possessing enhanced hydrophobic contacts between the toxin and receptor (Dutertre et al, 2005). As expected, PnIA(L5R A10L) binds to α3‐[V109A]β2 with an affinity over 10 times higher (0.34 nM, CI 0.30–0.38) than observed at the wild‐type receptor (4.6 nM, CI 3.69–5.83) (see Supplementary Figure 4). Interestingly, when this β2‐subunit mutant is coexpressed with the low affinity [D197A]α3 (2300 nM, CI 1780–2966), we observed a dramatic (>100‐fold) rescue of PnIA(L5R A10L) affinity (20.5 nM, CI 17.4–24.1). This rescue effect can be explained if the C‐terminal hydrophobic half of toxin repositions to interact with [V109A]β2, as seen in the Ac‐AChBP–PnIA(A10L D14K) co‐crystal structure (Celie et al, 2005a) compensating for the loss of the energetically favorable Arg5–D197 interaction. Due to conservation in the binding pocket, docking of TxIA(A10L) in the α7 homology model gave a similar overall result to that obtained using a α3β2 model. However, our experimental results show that, for this subtype, Arg5 is unlikely to interact with D195. TxIA(A10L) was therefore placed in the α7 binding pocket using the PnIA(A10L D14K) binding mode (Celie et al, 2005a) (Figure 5E). This orientation of the conotoxin does not allow a direct interaction between Arg5 and Asp195, explaining the lack of effect the α7‐D195A mutation. Instead, hydrophobic interactions with the complementary side (equivalent of the β‐subunit) dominate the binding interaction at α7.

Finally, mapping the α7 sequence to the AChBP crystal structure reveals an additional positive charge, Lys184 positioned where it could form an internal salt bridge with Asp195, thus reducing the likelihood of an interaction with Arg5 of TxIA(A10L). In addition, the downward tilt of TxIA(A10L) toward Asp195 might be prevented by a H‐bond expected between the TxIA‐Leu10 main chain and Gln115 in the α7 nAChR. Together, these observations support the possibility that TxIA(A10L) binds to α7 in a conformation observed for ImI and PnIA mutants in the AChBP subtypes. In such a conformation, the relevance of an Arg5‐Asp195 salt bridge would be minimized, as has been observed for ImI binding to AChBP. In contrast, the binding to the α3β2 nAChR subtype is likely to be similar to that observed in our AChBP/conotoxin complex, including an important contribution to binding from the Arg5‐Asp195 salt bridge.

Discussion

In this study, we demonstrate that an AChBP screen can be used to discover and guide the isolation of new α‐conotoxins in crude venom. This rapid and sensitive assay has advantages over fluorescent and electrophysiological methods used previously, and is amenable to high‐throughput applications. As all α‐conotoxins tested bound to Ls‐AChBP in the micromolar to mid nanomolar range, despite having distinct nAChR preferences for muscle and homomeric and heteromeric neuronal nAChR subtypes, it appears that Ls‐AChBP has retained ancestral nAChR features that allow a broad range of nAChR ligands to bind. In support, an Ls‐AChBP screen of over 30 different cone snail venoms revealed that all significantly displaced 125I‐Bgt binding. This high hit‐rate supports the hypothesis that each cone snail venom contains at least one nAChR antagonist (McIntosh et al, 1999). Given that many cone snails are molluscivorous, and the apparent broad distribution of AChBP in molluscs, AChBP could represent a previously unrecognized molecular target for α‐conotoxins with the potential to disrupt molluscan neurotransmission.

The sensitivity of an Ls‐AChBP screen is demonstrated with the isolation of α‐TxIA, a trace component of C. textile venom. The complete pharmacological characterization at Ls‐AChBP and nAChRs was subsequently achieved using an identical synthetic form. α‐TxIA was found to be the most potent α‐conotoxin acting at Ls‐AChBP reported to date and also had high affinity for certain mammalian nAChRs. Low nanomolar concentrations of α‐TxIA were sufficient to inhibit α3β2 nAChR, whereas 100‐fold higher concentrations were needed to block α7 nAChR current. In contrast, α‐OmIA, which also displays high‐affinity binding to AChBPs, is equipotent at α3β2 and α7 nAChRs (Talley et al, 2006). Sequence comparison of TxIA with other α‐conotoxins and synthesis of selected TxIA analogs revealed important contributions from hydrophobic residues at position 9 and 10 and the key role of Arg5 for high‐affinity interactions at Ls‐AChBP. Indeed, substitution of Arg5 in PnIA(A10L) produced a gain‐of‐function analog with similar properties to TxIA. The co‐crystal structure of Ac‐AChBP in complex with the higher potency analog TxIA(A10L), confirmed the crucial role of Arg5, which is coordinated by Asp195 and Tyr186, an interaction not seen in two other Ac‐AChBP–conotoxin complexes (Hansen et al, 2005; Celie et al, 2005a; Ulens et al, 2006). The presence of this salt bridge contributed to a 20° downward tilt of the toxin backbone when compared to PnIA(A10L D14K). An electrostatic interaction was also observed between Arg7 of conotoxin ImI and Asp195 in only one of the two available Ac‐AChBP co‐crystal structures (PDB accession codes 2BYP and 2C9T). However, mutant cycle analysis has shown that the interaction between Arg7 and Asp197 in nAChRs does not contribute to high‐affinity binding of conotoxin ImI (Quiram et al, 1999), most likely due to the different orientation of the toxin in the binding site. By mutating Asp195 in the background of Ac‐AChBP, we confirmed the functional importance of the electrostatic interaction between Arg5 and Asp195 as observed in the co‐crystal structure. Importantly, we observed that the affinity of PnIA(A10L D14K) remains unaffected by Asp195 mutations. This result provides strong evidence that the enhanced affinity of Arg5‐containing conotoxins can be attributed to an energetically favorable electrostatic interaction with Asp195 in Ac‐AChBP. In combination with electrophysiological recordings on mutant nAChRs, we demonstrated that this conclusion extrapolates to α3β2 nAChRs, but not to α7 nAChRs. As Asp195 is highly conserved among AChBPs and nAChRs, Arg5 TxIA may share a common set of binding interactions in AChBPs and certain nAChR subtypes.

The reorientation of TxIA(A10L) in the binding pocket of Ac‐AChBP is a surprising observation in light of the two other α‐conotoxin complexes that we and others have previously determined (Hansen et al, 2005; Celie et al, 2005a; Ulens et al, 2006). Such differences highlight that docking simulations based on the backbone orientation of PnIA(A10L D14K) (Talley et al, 2006) or contacts analysis based on superposition of the α‐conotoxin backbone (Clark et al, 2006) should be interpreted with caution, as these approaches may not adequately address residue changes or the reorientation of side chains in the toxin or receptor, which could generate backbone reorientations as observed for TxIA(A10L). However, from our analysis of homology models, it appears likely that TxIA(A10L) adopts the same orientation in α3β2 nAChRs as seen in our crystal structure, whereas it may adopt a PnIA‐like binding orientation in the α7 nAChR binding pocket. Given this result, it is somewhat surprising that TxIA has no affinity for α4β2 nAChRs despite the presence of an equivalent Asp residue and the close similarity to α3β2 nAChRs across the principal binding face. As no obvious clash could be identified during docking to an α4β2 homology model, it appears that AChBP is not a strong predictor of α4β2 structure, perhaps reflecting different docking pathways or an altered binding site structure.

In conclusion, we have demonstrated that Ls‐AChBP can be used to rapidly identify new ligands for nAChRs. By screening the crude venom of different cone snails, we discovered a new α‐conotoxin TxIA with enhanced subtype selectivity for α3β2 nAChRs. Co‐crystallization of the most potent analog TxIA(A10L) with Ac‐AChBP identified a new α‐conotoxin binding mode that was stabilized by a critical salt bridge between Arg5‐TxIA(A10L) and a highly conserved Asp residue on the principal face of the binding face of Ac‐AChBP. The functional importance of this interaction was confirmed through mutagenesis studies in different nAChR subtypes and AChBP. These results establish a structural framework for developing ligands with enhanced selectivity for the α3β2 nAChR. Engineering AChBPs with the ligand‐binding sites of specific nAChR subtypes, or with the ligand‐binding sites of other ligand‐gated ion channels, is expected to identify specific pairwise interactions underlying nAChR selectivity and further expand the potential of this protein scaffold to discover novel pharmacological probes.

Materials and methods

TxIA Isolation, sequencing and mass spectrometry

Venom from C. textile specimens was extracted and fractionated as described previously for other cone species (Lewis, 2000). Biological activity was tested using the Ls‐AChBP radioligand‐binding assay as described previously (Smit et al, 2001). This assay directed the final purification of the active compound on analytical RP‐HPLC (C18 Phenomenex column). A 20 pmol portion of pure peptide was Edman sequenced (Biomolecular Research Facility, Newcastle, Australia) on an Procise HT (Applied Biosystem). Molecular mass analysis of the native and synthetic peptides and LC‐MS analysis of crude C. textile venom were performed on a C18 Phenomenex column (2.1 × 150 mm, 5 μm) eluted with 0 to 60% B in 60 min (A=0.05% TFA; B=0.045% TFA, 90% ACN). Eluant was monitored with a PE‐Sciex API III triple quadrupole mass spectrometer (Thornhill, Ontario, Canada) over m/z 400–2000 and data analyzed using Analyst software (Agilent, CA, USA).

Binding assays

Competitive binding assays with His‐tagged Ls‐AChBP and 125I‐radiolabeled α‐bungarotoxin (specific radioactivity 5.5 TBq/mmol) were carried out as described previously (Smit et al, 2001). A binding assay was established using P2 rat brain homogenate as described previously (Rapier et al, 1990), with a final protein concentration of 6 mg/ml as determined by a BCA protein assay (Pierce, Rockford, IL, USA). Various concentrations of conotoxins diluted in 200 μl incubation buffer (50 mM HEPES at pH 7.4, 100 mM NaCl, 0.2% BSA) were incubated for 90 min in 100 μl P2 membrane with a final concentration of 3 nM 125I‐α‐bungarotoxin to measure binding to α7 nAChRs, or 1 nM 3H‐epibatidine (Amersham Biosciences, Castle Hill, Australia) plus 2 μM cold α‐bungarotoxin for non‐α7 nAChRs.

Binding assays with untagged Ac‐AChBP and D195 mutants were performed using 5 nM 3H‐epibatidine. Ligands were incubated in a white Optiplate‐96 (Perkin Elmer) with radioligand and protein (30–120 ng) in binding buffer (PBS, 20 mM Tris at pH 8, 0.05% Tween 20) in a final volume of 100 μl. FlashBlue GPCR beads (2 mg/ml) (Perkin Elmer) were added and after 90 min incubation and 16 h standing in the dark, the radioactivity was measured with a Wallac 1450 MicroBeta liquid scintillation counter. Binding‐data were evaluated by a nonlinear, least squares one‐site competition curve fitting procedure using Prism 4.01 (GraphPad Software Inc., San Diego, CA, USA).

Protein expression, purification and peptide synthesis

Untagged Ac‐AChBP was expressed from baculovirus in SF9 insect cells and purified from medium as described previously (Celie et al, 2004). Ac‐AChBP D195 mutants were constructed using a QuikChange approach (Stratagene, La Jolla, CA, USA) and verified using DNA sequencing. All peptides were synthesized using Boc chemistry with in situ neutralization protocols as described previously (Schnolzer et al, 1992). The oxidized peptides were purified by RP‐HPLC and analyzed by electrospray mass spectrometry.

Electrophysiology

cDNAs encoding neuronal nAChRs were provided by J. Patrick (Baylor College of Medicine, Houston, TX, USA) and subcloned into the oocyte expression vector pNKS2 (Dutertre et al, 2005). Site‐directed mutagenesis was performed with the QuikChange mutagenesis Kit (Stratagene, La Jolla, CA, USA) and primers were synthesized by MWG Biotech AG (Ebersberg, Germany). Sequences were verified by didesoxynucleotide sequencing (MWG Biotec AG). cRNA was synthesized from linearized plasmids with SP6 RNA polymerase using the mMessage mMachine kit (Ambion, Austin, TX, USA). Xenopus laevis frogs were purchased from Nasco International (Fort Atkinson, WI, USA). Oocytes were prepared as described previously (Dutertre et al, 2005) and injected with 50 nl aliquots of cRNA (0.5 μg/μl). Two‐electrode voltage‐clamp recordings were performed as described previously (Dutertre et al, 2005). Current responses to acetylcholine or nicotine were measured 1–10 days after cRNA injection at a holding potential of −70 mV using a Turbo Tec 05X Amplifier (NPI Electronic, Tamm, Germany) and Cell Works software. Currents were filtered at 200 Hz and digitized at 400 Hz. The perfusion medium was automatically switched using a custom‐made magnetic valve system. A fast and reproducible solution exchange (<300 ms) was achieved using a 50 μl funnel‐shaped oocyte chamber combined with a fast solution flow (∼150 μl/s) fed through a custom‐made manifold mounted immediately above the oocyte. Agonist pulses were applied for 2 s at 4 min intervals. Peptides were applied for three minutes in a static bath when responses to three consecutive agonist applications differed by less than 10%. EC50 values were calculated from a nonlinear fit of the Hill equation to the data (GraphPad version 3.0, San Diego, CA, USA). Data are presented as mean±s.e. from at least four experiments.

SPR spectroscopy

SPR spectroscopy was performed at 25°C on a Biacore T100 (Uppsala, Sweden). Proteins were immobilized on a CM5 chip using the amine coupling procedure where the proteins at 0.1 mg/ml concentration were flown over the chip at 5 μl/min in 10 mM sodium acetate at pH 4.0. Approximately 5000 response units (RUs) of Ac‐AChBP D195A and wild‐type Ac‐AChBP were immobilized on the chip and the empty flow cell was used as the control. Conotoxins (5–600 nM) in running buffer (25 mM sodium phosphate at pH 8.0, 100 mM sodium chloride) were injected across the chip at 30 μl/min. Biacore T100 evaluation software was used for analysis of the experimental data. GraphPad Prism (GraphPad version 4.0, San Diego, CA, USA) was used to generate final figures.

Crystallography

Crystals of Ac‐AChBP in complex with TxIA(A10L) were grown in nanoliter drops by mixing 200 nl protein solution with 200 nl reservoir solution composed of 200 mM sodium malonate, 20% polyethyleneglycol 3350 and bistrispropane at pH 8.5. The crystals belong to spacegroup P1 and have the following unit cell dimensions: a=72.54 Å, b=85.75 Å, c=121.67 Å, α=90.14°, β=80.01°, γ=70.64°. Glycerol was used as a cryoprotectant and incrementally added to the mother liquor to a final concentration of 30% before flash‐freezing the crystals by immersion in liquid nitrogen. Diffraction data were collected at beamline X06SA at the Swiss Light Source, Villigen. The resolution of observed reflections rapidly decayed from 1.8 to 2.8 Å during a 180° sweep due to radiation sensitivity of the crystals. In addition, the diffraction data showed signs of nonmerohedral twinning. The main crystal lattice was indexed with MOSFLM and data reduction and scaling was carried out with SCALA using the CCP4 program suite (CCP4, 1994). The protein structure was solved by molecular replacement with PHASER (McCoy et al, 2005) and the open C‐loop structure of Ac‐AChBP as the search model (PDB accession code 2C9T). The initial model was refined to Rwork=27% and Rfree=31% with REFMAC (Murshudov et al, 1997) using NCS and TLS restraints (Winn et al, 2001). Difference electron density maps clearly indicated the occupancy of all binding sites by TxIA(A10L). The α‐conotoxins were built into density with COOT (Emsley and Cowtan, 2004) using the structure of PnIA(A10L D14K) as a template (PDB accession code 2BR8). The model of Ac‐AChBP with TxIA(A10L) bound was then further refined to Rwork=24% and Rfree=30%. The issue of nonmerohedral twinning was addressed by reprocessing the diffraction data with EVAL14 (Duisenberg et al, 2003) and deconvoluting overlapping reflections from the interfering lattice. The resulting electron density map was characterized by a lower noise level, but higher R‐values for the refined protein model, which is expected due to lack of profile fitting in EVAL14 (Duisenberg et al, 2003). Further refinement of the structure was therefore carried out using MOSFLM‐processed data. Difference electron density peaks near most of the disulfide bridges in Ac‐AChBP and TxIA(A10L) indicated severe radiation damage. Therefore, diffraction data over a 360° sweep were collected on multiple segments of the crystal at beamline EH23‐2 of the European Synchrotron Radiation Facility, Grenoble. The beam was attenuated to minimize radiation sensitivity and a merged data set with improved statistics was obtained to 2.4 Å resolution including data to I/σI=1. The model was automatically rebuilt using pyWARP (Cohen et al, 2004) and has a Rwork=23% and Rfree=25% with good geometry after iterative cycles of manual rebuilding and refinement. Structure validation was carried out using WHATIF (Hooft et al, 1996) and MOLPROBITY (Davis et al, 2004). Full molecular replacement and refinement of the data to 2.7 Å, using a more conservative data cut‐off (I/σI=2), showed that the electron density did not change, but automatic rebuilding failed, indicating that the weak data contained significant information and that any errors in their measurement were sufficiently reduced by the use of maximum likelyhood refinement. Coordinates have been deposited in the Protein Data Bank with accession code 2UZ6. AREAIMOL and CONTACT were used to analyze interaction surface areas and contacts (CCP4, 1994). Interaction surface areas are reported as average±s.d. of binding sites occupied by conotoxin and in the context of the number of pentamers present in the asymmetric unit. Interactions between residues of conotoxins and Ac‐AChBP were only considered if present in at least three of five binding sites. Figures were prepared with PYMOL (DeLano Scientific, San Carlos, CA, USA).

Molecular modeling

The crystal structure of TxIA(A10L) bound to Ac‐AChBP was used as a template to build homology models of rat α7, α3β2 and α4β2 nAChRs following the method described by Dutertre et al (2005).

Supplementary data

Supplementary data are available at The EMBO Journal Online (http://www.embojournal.org).

Supplementary Information

Supplementary Information [emboj7601785-sup-0001.doc]

Acknowledgements

We thank Marion Loughnan for the gift of α‐conotoxins EI and [Y15]‐EpI, Alun Jones for mass spectrometry assistance, Laurent Billot for his help with statistical analysis, beamline staff at ESRF and SLS for assistance with data collection, Tassos Perrakis for advise on data collection and processing, members of the Sixma and Perrakis laboratory for comments and suggestions. Toine Schreurs and Loes Kroon‐Batenburg are acknowledged for processing data with EVAL, Serge Cohen for test driving pyWARP, Judith Smit for assisting with AChBP cloning and protein purification, Victor Tsetlin for donating PnIA(A10L D14K) and Heinrich Betz for generous support. This work was supported by an NHMRC Program Grant and Australian Research Council grant (RJL and PFA), a postgraduate scholarship from the University of Queensland (SD), the Deutsche Forschungsgemeinschaft NI 592/3 (AN) and a long‐term fellowship from the European Molecular Biology Organization (CU) as well as STW grant BBC6035 to TKS and ABS.

References

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