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Voltage-gated potassium (Kv) channels derive their voltage sensitivity from movement of gating charges in voltage-sensor domains (VSDs). The gating charges translocate through a physical pathway in the VSD to open or close the channel. Previous studies showed that the gating charge pathways of Shaker and Kv1.2-2.1 chimeric channels are occluded, forming the structural basis for the focused electric field and gating charge transfer center. Here, we show that the gating charge pathway of the voltage-gated KCNQ2 potassium channel, activity reduction of which causes epilepsy, can accommodate various small molecule ligands. Combining mutagenesis, molecular simulation and electrophysiological recording, a binding model for the probe activator, ztz240, in the gating charge pathway was defined. This information was used to establish a docking-based virtual screening assay targeting the defined ligand-binding pocket. Nine activators with five new chemotypes were identified, and in vivo experiments showed that three ligands binding to the gating charge pathway exhibit significant anti-epilepsy activity. Identification of various novel activators by virtual screening targeting the pocket supports the presence of a ligand-binding site in the gating charge pathway. The capability of the gating charge pathway to accommodate small molecule ligands offers new insights into the gating charge pathway of the therapeutically relevant KCNQ2 channel.
Voltage-gated potassium (Kv) channels represent the largest group of potassium channels and play crucial roles in a wide range of physiological processes1,2. Kv channels constitute potential drug targets for the treatment of diverse diseases ranging from cancers to metabolic, cardiovascular and neurological disorders3. The six transmembrane segments of Kv channels are grouped into the voltage-sensor domain (VSD) (S1-S4) and the pore domain (S5-P-S6). The voltage-sensing function of the VSD is conferred by charged residues, mostly arginines in S4. To open or close the channel, these charged residues translocate between the internal and external water-accessible crevices in the VSD through a physical gating charge pathway in response to membrane potential changes4. Studies on Shaker and Kv1.2-2.1 chimeric channels suggest that the pathway is occluded in the middle of the VSD5,6,7,8,9,10,11. A conserved phenylalanine in the middle of S2 (F290 of the Shaker channel and F233 of the Kv1.2-2.1 chimera channel), together with the nearby arginines of S4, was proposed to form the occluded site5,7,12. The phenylalanine separates the extracellular and intracellular hydrated crevices of the VSD and forms the charge-transfer center that catalyzes movement of the gating charges5,13. Substitutions of certain arginines of Shaker S4 by smaller amino acids create an omega pore in the mutated VSD, which is permeable to some cations (e.g., K+, Li+ and Cs+)7,12,14. The omega pore has been demonstrated to be the same as the gating charge pathway5, which has the proper size to accommodate an arginine side chain15. The occluded pathway is consistent with the focused electric field theory, i.e., the transmembrane electric field is focused on the occluded site by the internal and external water crevices7,16. In addition, several previous studies showed that the arginines along S4 are accessible to methanethiosulfonate reagents8,17,18, implying that small molecules might bind to this site. The compounds ICA-27243 and NH29 were also suggested to act on the VSD19,20. These studies shed light on the central structures of the gating charge pathways of the Shaker channel and the Kv1.2-2.1 chimeric channel, and raised the possibility of the gating charge pathway as a therapeutic target5,13.
KCNQ2 potassium channel (Kv7.2) is a low-threshold Kv channel. Opening of KCNQ2 channel or heteromultimeric KCNQ2 complexes below threshold will inhibit initiation of action potentials, and thus KCNQ2 plays a fundamental role in controlling neuronal excitability21. Mutations of human KCNQ2 genes that result in reduction or loss of channel activity cause benign familial neonatal convulsions. Activators capable of augmenting KCNQ2 function have been proven effective in treatment of human epilepsy22. In this study, we have identified an activator-binding pocket in the gating charge pathway of KCNQ2 by comprehensively employing homology modeling, molecular docking, molecular dynamics (MD) simulation, mutagenesis and electrophysiological determination. The small molecular activator that we recently discovered, ztz24023, was used as a probe for determining the binding model of ligands in the gating charge pathway. zt240 and two of the nine newly identified activators targeting the gating charge pathway exhibited comparable anticonvulsant activity as retigabine, a KCNQ activator approved as an anti-epilepsy drug in 201124. Our results offer insights into the gating charge pathway of KCNQ2 channel and demonstrate that the pathway can serve as a drug target for development of new therapeutics.
Compound ztz240 is a KCNQ2 activator identified recently23. Major effects of ztz240 on KCNQ2 channel include increasing outward current amplitude, left-shifting the voltage-dependent activation curve (G-V curve) and dramatic slowing of deactivation (Figure 1). The phenylalanine forming the occluded site in Shaker and Kv1.2-2.1 chimeric channels is highly conserved in the family of Kv channels with the degree of conservation of ~99%25. The corresponding conserved phenylalanine in KCNQ2 is F137, which is located around the suggested occluded site of gating charge pathway (Figure 1A and and1B;1B; Supplementary information, Figure S1A). The activator ztz240 is mainly composed of two aromatic rings with hydrophobic properties linked via an amide bridge; we therefore speculated that it may form hydrophobic interactions with F137 if the compound could access this residue. To test this idea, we performed mutagenesis on the conserved residue. Indeed, mutation of KCNQ2 F137 to alanine (F137A) dramatically reduced ztz240 activity (Figure 1C–1F). The right-shifted dose-response curve of KCNQ2 F137A further supports the critical role of F137 for the activity of ztz240 (Figure 1G). For the wild-type channel, the dose-response curve was a well-fit sigmoidal-shaped curve with an EC50 value of 2.81 μM. In contrast, the dose-response curve of KCNQ2 F137A could not be fit well, as potentiation is rather low even at higher concentrations.
One possible cause of the reduced sensitivity is that the transition into or out of open state of KCNQ2 channel is affected by F137A. However, negligible changing of biophysical parameters argues against F137A perturbing “state transition”. The tested biophysical parameters of KCNQ2 F137A, such as current density, half maximal activation voltage (V1/2), time constants of activation (closed to open transition) and deactivation (open to closed transition), are very similar to those of wild-type channel (Supplementary information, Figure S2A). In addition, F137A did not reduce the activities of other KCNQ2 activators. Retigabine, an activator recognizing a tryptophan in the S5 segment26,27, was tested first. KCNQ2 F137A exhibited similar sensitivity to 10 μM retigabine to wild-type channel (Supplementary information, Figure S2B). Next, ZnPy, another activator potentiating KCNQ channels through different mechanism from retigabine28, was found to potentiate wild-type and F137A KCNQ2 channels in comparable scales (Supplementary information, Figure S2C). NH29, the third activator reported to target the external part of the VSD20, also potentiated wild-type and F137A KCNQ2 channels in a similar manner (Supplementary information, Figure S2D). These data indicate that F137 is specifically critical for activity of ztz240.
F137 is located at the middle of the S2 segment of KCNQ2 VSD. We designed more mutants for the residues lining the VSD. Among the functional mutations, E130A, I134A, G138A, R207W and R210A dramatically decreased the potentiation activity of ztz240 in all three major aspects. They reduced the increase of outward current amplitude ratio (I/I0), and prevented or attenuated the left-shifting of the G-V curve (ΔV1/2) and the slowing of deactivation (Figure 2). The almost overlapping tail currents of these mutants with and without ztz240 clearly show the decreased effects on deactivation (Supplementary information, Table S1). In contrast, mutations S105A and M174A attenuated the left-shifting of G-V curve but did not decrease I/I0 ratio or prevent the slowing of deactivation (Figure 2 and Supplementary information, Table S1). Identification of multiple essential residues further indicates the importance of the VSD for ztz240 activity.
As the experimental structures of KCNQ2 and its complexes with other ligands have not been determined, it is challenging to construct a structural model for the ztz240-KCNQ2 interaction. Accordingly, a hierarchical strategy was used to construct the structural model by comprehensively employing homology modeling, molecular docking and MD simulation in conjunction with mutagenesis and electrophysiological determinations. The mutagenesis result suggests that the potential binding pocket of ztz240 is mostly located in the VSD rather than in other domains (Figure 1). Further electrophysiological experiments support that ztz240 binds to the open-state VSD (Supplementary information, Figure S3). Thus, we first built up a three-dimensional (3D) model for the transmembrane domain of KCNQ2 based on the structural information of the open-state Kv1.2 channel29,30,31 by using Discovery studio 2.6 (Supplementary information, Figure S1B).
Second, we constructed the binding model for ztz240 to KCNQ2. We defined a potential binding pocket for ztz240 according to the mutagenesis and electrophysiological data, which includes F137 and other residues essential for ztz240 to potentiate the channel (Figure 2 and Supplementary information, Table S1). Homology modeling could not predict proper conformations for the residues interacting with a ligand. Therefore, Induced Fit, a flexible docking program that considers the flexibilities of both ligand and side chains of a target protein, was applied to simulate the binding of ztz240 to KCNQ2. However, the current docking methods could not determine the orientation of ztz240 entering into the binding pocket, indicating that either end may enter into the pocket first (Supplementary information, Figure S4A). The orientation of ztz240 in the VSD was determined with the assistance of two derivatives of the compound (named YGP1 and YGP2) that have the fluorine and the chlorine substituted by hydrogen atoms, respectively. Electrophysiological recording showed that YGP1 still exhibited potentiation activity on KCNQ2 as ztz240 did; however, the potentiation activity of YGP2 was dramatically reduced (Supplementary information, Figure S4B and S4C). This result indicates that ztz240 may bind to the VSD via the configuration with chloropyridine forming the bottom of the pocket and the fluorophenyl located near the pocket entrance (Supplementary information, Figure S4B).
Third, the ztz240-KCNQ2 binding model derived from the docking simulation was further optimized by MD simulation. The MD simulation may overcome the shortage of docking simulation that could not consider the flexibility of the protein backbone32. The model of the tetramer of ztz240/KCNQ2 complex was embedded into a patch of 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC) bilayer and then subjected to a 200-ns MD simulation. The ligand-VSD interactions suggested by the optimized binding model are shown in Figure 3. ztz240 hydrophobically interacts with I134 and F137; the nitrogen atom of the linker forms hydrogen bonds with the side chain of E130; the pyridine ring is involved in a CH-π interaction with the α-hydrogen of R207; the chlorine atom forms an electrostatic interaction with the guanidyl of R210 and a halogen bond with the carbonyl oxygen of R207, respectively; the pyridine nitrogen forms another electrostatic interaction with the guanidyl of R210. Residues that have been identified as critical for the potentiation activity of ztz240 in the mutagenesis studies are directly involved in the ztz240-VSD interactions, which explains well the mutagenesis data (Figure 2 and Supplementary information, Table S1).
Most of the crucial residues lining the binding pocket are located in S2 and S4, such as E130, I134, F137, G138, R207 and R210, while very few residues in S1 and S3 affect the compound, such as S105 and M174 (Figure 3), which are not conserved in KCNQ isoforms. To further evaluate the roles of residues in the external segments of S1 and S3 in ztz240 activation, the remaining residues except those listed in Figure 2B and and2C2C were examined by alanine scanning, and none of them significantly affected ztz240 activity (Supplementary information, Table S1). These additional mutations and electrophysiological determinations retrospectively validate again our ztz240-KCNQ2 binding model.
The model of the ztz240-KCNQ2 interaction clearly describes a broad pocket in the VSD, extending from the extracellular mouth of the VSD to R210 (Figure 3C). This possible ztz240-binding pocket in KCNQ2 partially overlaps with the corresponding regions of the gating charge pathways of Shaker and Kv1.2-2.1 chimeric channels, though it is more expansive and deeper (Figures 1A and and3C3C)5,6,7,8,9,10,11,12,14,15. This result is consistent with previous studies indicating that the VSD of Kv channels might be druggable sites19,20. Our study further revealed that the gating charge pathway of KCNQ2 might have a new functionality, serving as a direct binding pocket for existing and newly designed activators such as ztz240 and new compounds discovered in this study (see below).
To discover new KCNQ2 activators and to further verify the possible activator-binding pocket, we carried out a structure-based virtual screen targeting the identified pocket, guided by the notion that if the identified binding pocket is reasonable, novel activators recognizing the identified ztz240-binding pocket could be discovered. The SPECS database containing ~200 000 chemicals was screened by docking approach. Twenty-five hits (YG001-YG025) were selected for bioassay. Nine compounds belonging to five different chemotypes displayed significant potentiation effects on the outward current of KCNQ2 channel (Figure 4). The potentiation ranges from 1.28 ± 0.06 to 3.56 ± 0.23 at 30 μM (Figure 4A). EC50 values of the three most potent active compounds, YG002, YG007 and YG025, were further revealed to be 4.64 ± 0.14 μM, 1.60 ± 0.16 μM and 5.92 ± 0.21 μM, respectively (Figure 4B). The μM-level EC50 is similar to the approved drug retigabine27. The scaffolds of the nine identified activators can be described as two aryl groups connected by a functional linker. The linkers can be divided into five chemotypes, thiourea (YG002 and YG014), hydrazide (YG006, YG009 and YG025), urea (YG007 and YG018), amide (YG021) and amine (YG023). YG021 is an analogue of the reported activator ICA-2724333, but the other four chemotypes have never been reported before as KCNQ activators. The key residues involved in the interaction of ztz240 with the VSD, such as F137 and R210, are still essential for the newly identified activators (Figure 4D). Consistently, both F137A and R210A mutations were found to differentially affect the activity of most of these newly identified ligands (Supplementary information, Figure S5). This result demonstrates again that the gating charge pathway of KCNQ2 may accommodate various activators.
A primary anti-epilepsy screening assay was performed to evaluate the activity of these compounds in mice using the maximal electroshock (MES)-induced seizure model. Among the tested activators, ztz240, YG007 and YG018 exhibited > 50% protection rate and thus were selected for further investigation in MES-induced and pentylenetetrazol (PTZ)-induced seizure models (Supplementary information, Table S2). Retigabine was set as the positive control. All three compounds exhibited excellent anti-epilepsy activity in both models. In the MES-induced seizure model, a single dose administration of the three compounds significantly prevented the tonic hind limb extension. The protection rates (100%, 90% and 90%) are comparable with that of retigabine (Table 1). In the PTZ-induced seizure model, the three compounds exhibited comparable anti-epilepsy activity as retigabine. A single dose of these compounds not only significantly delayed the clonus latency but also reduced the incidence of generalized tonic-clonic seizure (GTCS) and mortality (Table 2).
For many drug targets, such as GPCRs, nuclear receptors and ligand-gated ion channels, their functions are modulated by endogenous ligands. Accordingly, many drugs bind receptors at sites where the natural molecular activators (i.e., endogenous ligands) act34. In contrast, the binding site of Kv channel activators is more elusive, as the activation of Kv channels in the physiological environment is modulated by membrane potential rather than endogenous ligands. Elucidation of the binding of activators with Kv channels is essential both for understanding the mechanism of channel activation and for the development of therapeutics. To date, limited information about the binding site of activators of Kv channels is available. The present study provides evidence for the presence of a ligand-binding site in the gating charge pathway of KCNQ2 channel. The identified activator-binding site lying deeply inside the VSD is largely different from postulated sites reported previously, which are either located at the pore region or a superficial part of the VSD20,26,27. The newly identified site encases the activators through multiple transmembrane segments.
To characterize a ligand-binding site, crystallography of the ligand/protein complex is the most direct method. However, membrane proteins are notoriously difficult to purify and crystallize. Very few Kv channels have been crystallized successfully35,36,37, and no drug/Kv complex structure has been determined. Radioactive ligand-binding assays or photo-labeling experiments have not answered the question either. As a primary strategy for exploring the action sites of activators, mutagenesis experiments have been effective in identifying the key molecular determinants for potentiation on hERG and KCNQ channels38,39,40,41,42. However, the limitation of mutagenesis is the inability to exclude a binding site or a key site that is only essential for the activity of the compound, but not for binding. Our study provides an alternative way to distinguish binding sites from other key sites for channel modulators. We speculated that new activators would be found based on the 'binding site' by structure-based drug discovery if the 'binding site' is true. Structure-based virtual screening has been widely applied in drug discovery. A virtual screen of ~200 000 compounds in the SPECS database targeting this binding site was performed. Twenty-five hits were selected for biological validation and nine showed potentiation on KCNQ2 channel in the voltage clamp assay, which is considered as the 'gold standard' for the study of ion channels. The hit rate of our virtual screening is 36% (9/25), which is much higher than the hit rate (0.1%) of a cell-based high throughput screening for discovering KCNQ2 activators (http://pubchem.ncbi.nlm.nih.gov). In addition, the fact that all identified novel activators recognized the same site further supports the presence of the ligand-binding site. It should be noted that the complex model was built based on a homology model of KCNQ2 channel, which may contain several inherent limitations. There is no representation of cation-π interaction and halogen bond in empirical force fields. Molecular docking and MD simulation applied in the current work could not fully characterize these interactions. These particular interactions were proposed based on geometric considerations. Further crystallography or combined quantum mechanics/molecular mechanics (QM/MM) studies are necessary to fully elucidate the binding mode of ztz240 in the binding pocket.
The occluded gating charge pathways of Shaker and Kv1.2-2.1 chimeric channels focus the electric field on a narrow region and form the charge-transfer center, both of which were suggested to be important for the mechanism of voltage gating of Kv channels. This study shows a new functionality of the gating charge pathway of KCNQ2, which serves as a direct binding pocket for activators. The broad pocket in the VSD extends from the extracellular mouth of the VSD to R210 (Figure 3C) and allows chemical ligands to enter and reside in the space beneath R207. The volume of this space is ~170 Å3, which is large enough to accommodate the aromatic rings of ztz240 and our newly identified ligands (moieties highlighted in orange in Figure 4D) with sizes of 90 to 140 Å3. The ability of the KCNQ2 VSD to bind chemical ligands suggests that the gating charge pathway of the channel might be structurally different from other Kv channels, such as the Kv1.2-2.1 chimera. The phenylalanine (F233) is the key residue of the charge-transfer center in the Kv1.2-2.1 chimera. When it was substituted by 19 other natural amino acids, the voltage dependence of most mutants was largely affected13. However, analogous mutations F137X (X represents the other 19 natural amino acids) cause much less influence on the voltage dependence of KCNQ2 channel gating (Supplementary information, Figure S6). First, all 19 KCNQ2 mutants are functional, whereas only 15 Kv1.2-2.1 mutants are functional. When the phenylalanine is mutated to aspartic acid (D), lysine (K) or arginine (R), the KCNQ2 channels are still functional while the Kv1.2-2.1 channels lose functionality, suggesting that the phenylalanine (F137) in KCNQ2 is more tolerant to changes. Second, effects of the mutations on G-V curves are different. Among the 15 functional Kv1.2-2.1 mutants, 13 exhibit largely right-shifted G-V curves with positive V1/2 and the right-shifting effects are > 100 mV for some mutants, such as F233A13. Only two mutations, tryptophan (W) and tyrosine (Y), exhibit currents near wild-type levels with negative V1/2, which is consistent with the notion that a rigid cyclic side chain is important at this position13. In contrast, for KCNQ2, only six mutants display positive V1/2 values and the right-shifting is < 100 mV for all the mutations. Furthermore, besides F137W and F137Y, F137A, F137V, F137I and F137L also exhibit similar V1/2 values to that of the wild type, suggesting that the cyclic side chain at F137 position is not as important as in the Kv1.2-2.1 chimera. However, for some specific substitutions, the mutations lead to similar kinetic effects for the two channels. For instance, both Kv1.2-2.1 F233W and KCNQ2 F137W exhibit a slower rate of closure than wild-type channels (Supplementary information, Figure S6C and S6D)13. The discordant phenotypes of the F137X and F233X mutants support the idea that gating charge pathways are different at this particular position. Other explanations for discordant phenotypes between KCNQ2 and Kv1.2-2.1 chimeric channels are possible. Interestingly, the present concept of diverse gating charge pathways is in agreement with the observation that the voltage-gated proton channel Hv1 forms an internal water wire penetrating the whole VSD43,44,45. The Hv1 channel only contains four transmembrane segments homologous to the VSD of Kv channels, but lacks the classic pore domain of other voltage-gated ion channels.
Although there is no available atomic-resolution structure of a Kv channel in the resting state, the first four arginines (R1-R4) of Kv1.2 are generally thought to stay in a 'down' position in the resting state compared with the open state46,47. A recent long-time all-atom MD simulation also supports the downward movement of arginines5. The aromatic moieties of ztz240 and other identified activators reside in the gating charge pathway by filling the space between R207 and R210, thereby preventing the arginine from moving down to its resting state (Figure 5 and Supplementary information, Movie S1). The capability of the KCNQ2 VSD to accommodate chemical ligands allows the possibility to upregulate Kv channel function and treat diseases through acting at the gating charge pathway directly. This notion was examined by in vivo experiments. Anti-epilepsy effects of ztz240 and the nine newly identified activators were tested in the mouse MES-induced seizure model. Among them, ztz240, YG007 and YG018 exhibit anti-epilepsy activity and protection rates comparable to that of retigabine (Table 1). Different from ztz240, retigabine activates KCNQ2-5 through a crucial tryptophan residue in S526,27. As KCNQ channels are accessible to various types and combinations of pharmacological regulation28, ztz240 and retigabine may lead to a synergistic effect, which might be beneficial for treatment of epilepsy. In summary, our study provides new insights into the structures and functions of gating charge pathways of Kv channels. The discovery of new modulators targeting the gating charge pathway by virtual screening may have general implications for other voltage-gated ion channels.
Starting from KCNQ cDNAs, the KCNQ2 point mutants were constructed by recombinant PCR and verified by sequencing.
Chinese Hamster Ovary (CHO) cells were grown in 50/50 DMEM/F12 (Cellgro, Manassas, VA, USA) with 10% fetal bovine serum (FBS) and 2 mM L-glutamine (Gibco, Carlsbad, CA, USA). To express ion channels, cells were split at 24 h before transfection, plated in 60-mm dishes and transfected with Lipofectamine 2000™ reagent (Invitrogen, Carlsbad, CA, USA), according to the manufacturer's instruction. At 24 h after transfection, cells were split and replated onto coverslips coated with poly-L-lysine (Sigma-Aldrich, St Louis, MO, USA). A plasmid for cDNA of GFP (Amaxa, Gaithersburg, MD, USA) was co-transfected to aid the identification of transfected cells by fluorescence microscopy.
Whole-cell voltage clamp recording was carried out at room temperature in CHO cells with an Axopatch-200B amplifier (Molecular Devices, Sunnyvale, CA, USA). The electrodes were pulled from borosilicate glass capillaries (World Precision Instruments, Sarasota, FL, USA). When filled with the intracellular solution, the electrodes had resistances of 3-5 MΩ. Pipette solution contained: KCl 145 mM, MgCl2 1 mM, EGTA 5 mM, HEPES 10 mM and MgATP 5 mM (pH 7.3 with KOH). During the recording, constant perfusion of extracellular solution was maintained using a BPS perfusion system (ALA scientific Instruments, Westburg, NY, USA). Extracellular solution contained: NaCl 140 mM, KCl 3 mM, CaCl2 2 mM, MgCl2 1.5 mM, HEPES 10 mM and glucose 10 mM (pH 7.4 with NaOH). Signals were filtered at 1 kHz, and digitized using a DigiData 1440 with pClamp 9.2 software (Molecular Devices). Series resistance was compensated by 60%-80%.
All animal procedures were performed in accordance with the National Institutes of Health Guide for the Care and Use of Laboratory Animals, under protocols approved and strictly followed by the Institutional Animal Care and Use Committees (IACUC). The IACUC checked all protocols and approved this study. Male KM mice, weighing 18-22 g, were obtained from Shanghai SLAC Laboratory Animal CO Ltd. For the MES-induced seizure model, the shock level was set at 160 V and the duration was set at 5.4 s with continuous wave under the eighth configuration, using a physiological and pharmacological electronic stimulator (Jinan, Shandong, China). The day before the experiment, the mice with GTCS induced by MES were prepared for the tests of the anticonvulsant effects of the compounds. Mice were separately administered with the testing compounds or vehicle in 5% dimethylsulfoxide/95% (0.2%) hydroxymethyl cellulose by intraperitoneal injection 30 min before electroshock application in the mouse; the compound retigabine was used as the positive control. The incidence of hind limb extension was recorded, and if extension did not occur in the experiment, the animal was thought to be protected against the MES-induced seizure. For the PTZ-induced model, compounds were prepared in the same way as those in the MES-induced model and administered to male KM mice by intraperitoneal injection in a volume of 0.2 ml/10 g 30 min before administration of 100 mg/kg PTZ sc. The latency to clonic seizure was recorded in seconds, and the incidence of GTCS and mortality rate caused by PTZ were both measured in this test.
To a solution of benzoic acid (0.36 mmol) in 2 ml THF at 0 °C, N,N′-dicyclohexylcarbodiimide (DCC) was added with stirring for 30 min. 6-chloropyridin-3-amine (0.3 mmol) was then added to the mixture followed by addition of dimethyl aminopyridine (DMAP, 0.06 mmol) at room temperature with stirring overnight. After evaporating the volatiles, the mixture was partitioned by CH2Cl2 (2 × 20 ml) and saturated with NaHCO3 solution (20 ml), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by column chromatography to give the compound YGP1 with 82% yield. HPLC (Agilent 1100; column/Extend-C18, 5 μm, 4.6 × 150 mm; methanol:water/60:40; 0.6 ml/min), > 98%; 1H NMR (400 MHz, CD3OD) δ 8.73-8.72 (m, 1H), 8.26-7.23 (m, 1H), 7.96-7.93 (m, 2H), 7.62-7.58 (m, 1H), 7.54-7.46 (m, 2H), 7.44 (d, J = 0.8 Hz, 1H); 13C NMR (125 MHz, CD3OD) δ 167.54, 145.11, 141.35, 135.28, 134.05, 131.95, 131.26, 128.34, 127.35, 124.06; MS (ESI) m/z: 233 [M+H]+; HRMS (ESI) 255.0301 Calcd for C12H9N2OClNa, found 255.0311 [M+Na]+.
To a solution of 4-fluorobenzoic acid (0.36 mmol) in 2 ml THF at 0 °C, DCC was added with stirring for 30 min. Then, pyridin-3-amine (0.3 mmol) was added to the mixture followed by addition of DMAP (0.06 mmol) at room temperature with stirring overnight. After evaporating the volatiles, the mixture was partitioned by CH2Cl2 (2 × 20 ml) and saturated with NaHCO3 solution (20 ml), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by column chromatography to give the compound YGP2 with 85% yield. HPLC (Agilent 1100; column/Extend-C18, 5 μm, 4.6 × 150 mm; methanol:water/60:40; 0.6 ml/min), > 99%; 1H NMR (CDCl3, 400 MHz): δ 8.65(d, 1H), 8.38(dd, 1H), 8.28(m, 1H), 8.10 (s, 1H), 7.92 (m, 2H), 7.33(t, 1H), 7.16(dd, 2H); 13C NMR (125 MHz, CDCl3+CD3OD): δ 166.3, 164.1, 144.5, 141.4, 135.9, 130.5, 130.1 × 2, 128.6, 124.0, 115.6 × 2. MS (ESI) m/z: 217 [M+H]+; HRMS (ESI) 239.0597 Calcd for C12H9N2OFNa, found 239.0592 [M+Na]+.
Compounds purchased from SPECS were purified before bioassay. The purity of the compounds listed in Figure 4B has been determined by HPLC to be ≥95%.
KCNQ2 structures were modeled based on the structural information of the open-state Kv1.2 channel29,30,31 by using Discovery studio 2.6 (Accelrys Inc., San Diego, CA, USA). Multiple sequence alignment was generated by using CLUSTALW web server (http://www.ebi.ac.uk/Tools/msa/clustalw2)48. The highly conserved residues were used to guide the alignment (Supplementary information, Figure S1A), and the alignment was manually adjusted based on the transmembrane regions in the Kv1.2 structures30,31,49. The result of the sequence alignment is shown in Supplementary information, Figure S1A. The S4-S5 linker, S5, and S6 regions of Kv1.2 and KCNQ channels are highly conserved, which directly provides a reliable basis for mapping the positions of these regions of KCNQ channels based on the structure of Kv1.2 channel. The secondary structure and transmembrane domain were predicted by I-TASSER server50 to guide the modeling of the S1-S4 helix. Although residues are not so highly conserved in S1-S4 segments as those in S5 and S6 segments, the conserved residues, E0, E1, D3, R1, R2, R3, R4 and R5, provided enough information to locate the positions of S1-S4 (Supplementary information, Figure S1A). The conserved phenylalanine of S2 also helped to map the position of S2. As a result, the positions of S1-S4 could be accurately mapped. The modeled structure of KCNQ2 channels underwent a 20 000-step energy minimization in AMBER 1051.
MD simulations were performed on two systems — the KCNQ2 tetramer and the tetramer of the ztz240/KCNQ2 complex. MD simulation of KCNQ2 was started from the homology model of KCNQ2, and simulation of the complex started from the docking model of ztz240 to the KCNQ2 homology model. The starting structures of the three systems were embedded in a patch of POPC bilayer generated by using VMD52, and then solvated by TIP3P water molecules53. MD simulation was carried out by using GROMACS 4.5354. The CHARMM27 force field with CMAP correction was applied55,56,57; ztz240 parameters were generated by SWISSPARAM web server (http://www.swissparam.ch/)58. Na+ and Cl− ions were added to maintain neutralization of the system. The NPT ensemble and 3D periodic boundary conditions were applied in the MD simulation, with the time step of 2 fs. The LINCS algorithm59 was used to constrain the bond lengths. A constant pressure of 1 bar was applied with a coupling constant of 1.0 ps using Berendsen algorithm60. The v-rescale method61 was employed to keep the temperature constant (300 K), with a coupling constant of 1.0 ps. The Particle-Mesh Ewald (PME) method62 was used to handle the long-range electrostatics with a real-space cut-off of 1.2 nm. The bilayer was first equilibrated to 10 ns with the protein and ztz240 fixed. The systems of KCNQ2 tetramer and ztz240/KCNQ2 complex were submitted to 50-ns and 200-ns production runs, respectively.
Docking was performed by using Glide (Schrödinger, LLC, New York, NY, USA). Receptor was prepared by using the Protein Preparation and Grid Preparation tools in the Schrödinger Maestro interface. Hydrogen orientations were optimized in protein preparation module. The docking box was set to cover the assumed binding pocket and centered at E130 and R207, which were supposed to be the middle of the potential pocket. The default settings were adopted for the cut-off, neutralization, scaling and dimension of the binding pocket. According to the primary mutagenesis and electrophysiological results, we noticed that ztz240 may access F137. Homology modeling could not predict proper conformations for the residues interacting with a ligand. Therefore, we applied the Induced Fit module encoded in the Schrödinger modeling package (Schrödinger, LLC). Inducted Fit is a flexible docking method that may consider the flexibilities of both the side chains of protein resides and small molecules during docking simulation. F137 and residues around F137 in the central part of VSD, E130, R207, S179, Q204, T133 and I134 were treated as flexible residues.
The modules of High Throughput Virtual Screening (HTVS) and Standard Precision (SP) were used as filters sequentially in the virtual screening. From the commercially available SPECS database, ~20 000 compounds were screened and the top 700 compounds with highest G-score values were inspected. Compounds with the docking positions showing high-energy conformations, such as unreasonable angles and torsions caused by the steric effect, were excluded. Among the remaining compounds, molecules with molecular weight > 500 and those with large subgroups outside the pocket were also removed. The absorptions of the remaining potential hits were predicted by using Pipeline Pilot (Accelrys). AlogP < 5 and Absorption_Level = 0 were taken as filters. Finally, 25 compounds were selected as hits for bioassay.
The sizes of the pockets in the KCNQ2 channel were calculated by using the program of POVME63. The sizes of ligands and the side chain of arginine were measured by the web server Molinspiration (http://www.molinspiration.com/).
Patch-clamp data were processed using Clampfit 9.2 (Molecular Devices), and then analyzed in Graphpad Prism 4 (GraphPad Software, San Diego, CA, USA). Voltage-dependent activation curves were fit with the Boltzmann equation: G = Gmin+ (Gmax − Gmin)/(1 + exp(V − V1/2)/S)), where Gmax is the maximum conductance, Gmin is the minimum conductance, V1/2 is the voltage for reaching 50% of maximum conductance and S is the slope factor. Dose-response curves were fit with the Hill equation: E = Emax/(1 + (EC50/C)P), where EC50 is the drug concentration producing half of the maximum response and P is the Hill coefficient. The deactivation traces were fit with exponential equations containing one or two components using Clampfit 9.2. Data are presented as means ± SEM. Significance was estimated using paired two-tailed Student's t-tests.
We gratefully acknowledge the financial support from the State Key Development Program for Basic Research of China (2013CB910604 and 2009CB918502), the National Natural Science Foundation of China (81072579, 81173027, 21021063 and 81230076), Shanghai Science and Technology Development Funds (12QA1404000), and the National Institute of Health (MH084691 and GM070959). Computational resources were supported by National Supercomputing Center in Tianjin and Shanghai Supercomputer Center. We thank Professor Rolf Hilgenfeld (University of Lübeck, Germany) for his help in English language editing.
(Supplementary information is linked to the online version of the paper on the Cell Research website.)
The homology model for the transmembrane domain of the KCNQ2 tetramer.
Biophysical properties of F137A and sensitivity of F137A to different activators.
Electrophysiological experiments indicated ztz240 can bind to the open-state VSD.
Orientation of ztz240 within the binding site.
F137 and R210 are critical for most identified ligands.
Voltage dependence of F137X.
Effects of ztz240 on VSD mutants
Primary antiepilepsy screening of ztz240 and newly identified activators on mouse MES-induced seizure model
The potentiation mechanism of KCNQ2 channel by ztz240.