Fenofibrate Recognition and Gq Protein Coupling Mechanisms of the Human Cannabinoid Receptor CB1
CAS Key Laboratory of Quantitative Engineering Biology, Institute of Synthetic Biology, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518055, China
iHuman Institute, ShanghaiTech University, 393 Middle Huaxia Road, Pudong, Shanghai, 201210, China
Institute of Biophysics, Chinese Academy of Sciences, 15 Datun Road, Chaoyang District, Beijing, 100101, China
School of Life Sciences, University of Chinese Academy of Sciences, Beijing, 100049, China
Key Laboratory of Biomacromolecules, Chinese Academy of Sciences, Beijing, 100101, China
Abstract
The G‐protein‐coupled human cannabinoid receptor 1 (CB1) is a promising therapeutic target for pain management, inflammation, obesity, and substance abuse disorders. The structures of CB1‐Gi complexes in synthetic agonist‐bound forms have been resolved to date. However, the commercial drug recognition and Gq coupling mechanisms of CB1 remain elusive. Herein, the cryo‐electron microscopy (cryo‐EM) structure of CB1‐Gq complex, in fenofibrate‐bound form, at near‐atomic resolution, is reported. The structure elucidates the delicate mechanisms of the precise fenofibrate recognition and Gq protein coupling by CB1 and will facilitate future drug discovery and design.
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Keywords: cryo‐electron microscopy, fenofibrate, Gq coupling, human cannabinoid receptor 1, ligand recognition
Graphical
The cryo–EM structure of CB1‐Gq complex, in fenofibrate‐bound form, is resolved to elucidate the ligand selectivity of fenofibrate and Gq coupling mechanism to CB1, providing a structural understanding of ligand recognition and Gq coupling mechanisms of CB1.
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Article notes
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Revised 2023 Dec 21; Received 2023 Sep 2; Collection date 2024 Apr.
1.Introduction
CB1 is the principal target of Δ9‐tetrahydrocannabinol (THC), a psychoactive chemical from Cannabis sativa L. with a wide range of therapeutic applications and recreational uses for more than 5000 years.[ 1 , 2 ] CB1 also mediates diverse pathophysiological effects of endocannabinoids like anandamide (AEA) and 2‐arachidonoyl glycerol (2‐AG),[ 3 , 4 ] and numerous synthetic cannabinoids[ 5 ] by coupling to G proteins of the Gi/o and Gq classes.[ 6 , 7 ] As the most abundant receptor in the mammalian brain,[ 1 ] CB1 mainly distributes in the central nervous system and exerts regulatory influence over cognitive functions, memory, and motor control by modulating neurotransmitter release, which is regarded as one important target of mental illness such as depression and anorexia nervosa.[ 8 ]
Fenofibrate, ranked among the world's top 200 drugs by sales, is widely prescribed for treating primary hypercholesterolemia, mixed dyslipidemia, and hypertriglyceridemia. Acting through peroxisome proliferation‐activated receptor (PPAR), fenofibrate effectively lowers blood cholesterol and triglyceride levels.[ 9 ] Beyond its lipid‐lowering effects, fenofibrate has demonstrated central nervous system pharmacological impacts, including antidepressant‐like effects in mice[ 10 ] and neuroprotection against Parkinson's disease. Notably, these effects may be mediated through the CB1 signaling pathway, as Fenofibrate has been identified as a partial agonist of CB1.[ 11 , 12 ]
While various active and inactive CB1 structures in synthetic cannabinoid‐bound forms have been resolved to clarify the ligand selectivity,[ 13 , 14 , 15 , 16 , 17 , 18 , 19 ] the commercial drug recognition and Gq coupling mechanisms of CB1 remain obscure. The lack of experimental structure of fenofibrate‐bound CB1‐Gq complex has hindered understanding of the pathophysiological function underlying CB1 signaling. Herein, we report the cryo‐EM structure of CB1‐Gq complex, in fenofibrate‐bound form, to unravel the ligand selectivity of fenofibrate for CB1 and shed light on the Gq coupling mechanism, providing a structural understanding of ligand recognition and Gq coupling mechanisms of CB1.
2.Results and Discussion
2.1.Overall Cryo‐EM Structure of the Fenofibrate‐Bound CB1 Complex
In our study, the calcium‐induced luciferase accumulation assays indicated that fenofibrate could activate CB1 through Gq signaling pathway (Figure 1A,B). To obtain a stable and homogeneous cyro‐EM sample, we introduced the miniGs/q protein and employed the NanoBiT strategy to stabilize the fenofibrate‐bound CB1‐Gq complex.[ 20 , 21 ] The CB1, miniGs/q protein and β1γ2 were expressed in HEK293F, Escherichia Coli and sf9 cells, respectively. These proteins were purified and assembled in vitro with the addition of fenofibrate and Nb35,[ 22 ] which stabilizes the nucleotide‐free complex by bridging the miniGs/q and Gβ1γ2 subunits. All of these components were identified through SDS‐PAGE analysis (Figure S1, Supporting Information). The structure was determined using single‐particle cryo‐EM, yielding an overall resolution of 2.9 Å (Figure 1C; Figure S2 and Table S1, Supporting Information). The high‐quality cryo‐EM map enabled accurate modeling of the 7TM elements of the CB1 receptor, the miniGs/qβ1γ2 heterotrimer, and Nb35. Notably, the side chains of most residues are well defined in all components (Figure S3, Supporting Information). Furthermore, fenofibrate was unequivocally identified within the orthosteric pocket of CB1 (Figure 1C).
2.2.Fenofibrate Recognition by CB1
In elucidating the interaction details between CB1 and fenofibrate, we observed substantial structural rearrangements within the orthosteric pocket of the fenofibrate‐bound CB1 complex. While the agonist fenofibrate adopted an L‐shape conformation closely resembling that seen in other agonist‐bound CB1 structures (Figure S4, Supporting Information), notable distinctions emerged within the orthosteric pocket. The interactions between fenofibrate and CB1 are mainly hydrophobic and aromatic, consisting of residues from extracellular loop 2 (ECL2), transmembrane helices (TM) 2, 3, 5, and 6 (Figure 2A). Specifically, the benzene ring (Ring1) of fenofibrate engaged in π–π interaction with the residue F1742.61 (superscripts indicate Ballesteros‐Weinstein numbering for GPCRs[ 23 ]). Additionally, fenofibrate was involved in extensive hydrophobic interactions with the residues F1702.57, F1772.64, L1933.29, T1973.33, F2003.36, Y2755.39, L2765.40, W2795.43, L3596.51, and F268ECL2 (Figure 2A,B). These interactions were further confirmed by mutagenesis analysis (Figure 2C). Of note, the carbonyl group at the C12 position of fenofibrate forms an additional hydrogen bond with the residue S1732.60 (Figure 2A), which was also observed in the CP55940 binding pocket.[ 24 ] Furthermore, the alignment map of CB's agonists binding pocket indicated that fenofibrate adopted a different barcode for CB1 interaction compared to other agonists‐bound CB1 structures (Figure 2D), perhaps accounting for the fenofibrate recognition specificity of CB1.
To further identify the stability of fenofibrate in the orthosteric pocket, the molecular dynamics (MD) simulation was carried out to elaborate the interaction between fenofibrate and CB1. During two parallel 200 ns canonical NPT ensemble simulations, we found that the fenofibrate remains a relatively constrained conformation but may exist as a flexible binding mode, as reasoned from root mean square deviations (RMSD) and quite diverse contact frequency of fenofibrate with surrounding residues during simulation (Figure 3A; Figure S5, Supporting Information). Two simulations brought fenofibrate into two different “Ring 1” orientations (Figure 3C). As expected, the residue S1732.60 kept quite close contact as the same in an initial model in two simulations (Figure 3B,C). Along with prevalent hydrophobic and van der Waals interactions, fenofibrate was caged in the orthosteric‐binding pockets.
2.3.The Gq Coupling Mechanism of CB1
Owing to the lack of the experimental structure of CB1‐Gq complex, the detailed interaction mechanism between CB1 and Gq is still ambiguous. The structure of CB1‐miniGs/q complex uncovered that the interaction between miniGs/q and CB1's cytoplasmic cavity was mainly contributed by the transmembrane helices TM3, TM5, TM6, and TM7 in CB1. The CB1‐Gq complex exhibited a global structure resembling other Gq‐bound receptors, although a noticeable deviation in the α5‐helix distinguished it from the Gq protein in the GPR139‐Gq complex[ 25 ] (PDB code: 7VUH), resulting in an 18° relative rotation of the Gq protein (Figure S6, Supporting Information). In contrast, a comparison of the miniGs/q‐ and Gi‐CB1 (PDB code: 6KPG) structures revealed no specific conformational differences between the receptors (Figure 4A), which differed from the human glucagon receptor.[ 26 ] However, the α5‐helix of the Gq protein displayed a 40° clockwise rotation compared to that of the Gi protein (Figure 4B). This disparity suggests that CB1 adopts a unique coupling mode with the Gq protein, attributed to closer contacts between the α5‐helix of Gq and TM3 of CB1 (Figure 4B). We propose that the ability of CB1 to accommodate the α5‐helix of Gq serves as a determinant of Gq coupling specificity.
The interaction between the Gq protein and CB1 involved both polar and hydrophobic interactions. Specifically, the residue K4028.48 established the hydrogen bonding interactions with the O atoms of R379 and L383 in the Gq’s α5‐helix, while the residue N377 formed the hydrogen bonding interaction with the hydroxyl group of S2173.53. Additionally, the residue N382 from Gq’s α5‐helix formed the polar interaction with E3406.32. Moreover, the hydrophobic side chains of L383, Y381, and L378 on Gq protein directed toward the hydrophobic pocket (I2183.54, I2975.61, A3015.65, and L3416.33) of CB1 (Figure 4C). Mutations of these residues impaired the calcium‐induced luciferase accumulation of CB1 (Figure 4D). To illustrate the key residues of CB1 for the determinants of Gq or Gi coupling specificity, we performed a sequence alignment of the CB1 positions bound by the α5‐helix of Gq and Gi protein (PDB code: 6KPG). We observed significant differences in the detailed interactions of CB1 with Gq or Gi proteins, except for the residues I2975.61 and L3416.33 (Figure 4E).
3.Conclusion
In summary, the cryo‐EM structure reported in our study reveals the molecular recognition mechanism behind the precise recognition of the commercial drug fenofibrate by CB1. Fenofibrate was consolidated in the orthosteric pocket through hydrogen bonding interaction with the residue S1732.60, as well as through hydrophobic interactions. This work will facilitate further research into the pharmacological effects of fenofibrate on the human body and promote the design of new highly selective drugs targeting CB1 by comparing the similarities and differences in the recognition mechanisms of endogenous ligands, synthetic cannabinoids, and commercial drugs by CB1.[ 27 ] Furthermore, the determined structures of CB1‐G protein complexes in previous studies mainly focused on Gi pathway. We first determined the cyro‐EM structure of CB1‐Gq complex and elucidated the coupling mechanism between CB1 and Gq protein. CB1 adopts the different coupling barcodes to recognize Gq and Gi proteins, respectively. This structure provides new insight into G protein selectivity of CB1 activation and a structural basis for designing highly selective drugs of CB1.
4.Experimental Section
Materials and General Procedures
Fenofibrate was purchased from InnoChem Science & Technology. The detergent Lauryl Maltose Neopentyl Glycerol (LMNG) and Synthetic drop‐in substitute for Digitonin glyco‐diosgenin (GDN) used for receptor solubilization were purchased from Anatrace. Cholesterol hemisuccinate (CHS) was purchased from Sigma–Aldrich. Components of CB1‐fenofibrate‐miniGs/q‐Nb35 complex are expressed separately and assembled in vitro. Protein purification was performed at AKTA avant system.
Calcium‐Induced Luciferase Accumulation Assay
The HEK293T cells were plated in 24 well plates and transfected with pGL4.30[luc2P/NFAT‐RE/Hygro] vector and wild‐type CB1 vector or CB1‐mutant vector by using Lipofectamine 2000. After 24 h, the cells were washed with PBS and treated with different concentrations of fenofibrate for 12 h. Then, the cells were harvested and lysed with passive lysis buffer contained in a luciferase reporter assay kit (Promega). The luciferase activity was normalized by protein amounts of cell lysates. The protein concentration was determined using a bicinchoninic acid (BCA) protein assay kit. The data are processed by graphpad prism10 and shown as the mean ± s.e.m. from three independent measurements.
Expression and Purification of CB1
The construct of CB1 was modified from previously reported.[ 19 ] Human wild‐type CB1 with the truncations of the residues 1–70 and 426–472, and the mutations (T210I, E273K, T283V, and R340E) was subcloned into a modified pTT5 mammalian expression vector containing a haemagglutinin (HA) signal sequence, a FLAG tag, 10×His tag and a tobacco etch virus (TEV) protease cleavage site at N‐terminus, followed by a thermostabilized BRIL and a PreScission protease site before CB1 sequence. Additionally, a LgBiT sequence was fused to the C‐terminal of the modified CB1 for increasing complex stability.[ 20 ] CB1 was expressed in HEK293F cells using FreeStyle 293 Expression system (Invitrogen), and purified as previously described[ 19 ] with the addition of 50 µm fenofibrate. Briefly, the cell pellet was lysed by hypotonic buffer (10 mm HEPES pH 7.5, 10 mm MgCl2, 20 mm KCl) for 2 h at 4 °C and centrifuged at 35 000 rpm for 30 min. The precipitate was washed once again by using a hypotonic buffer. Then the crude membrane was washed by hypertonic buffer (10 mm HEPES pH 7.5, 10 mm MgCl2, 20 mm KCl, 1 m NaCl) three times, and resuspended in cryopreservation solution (the hypotonic buffer supplemented with 30% glycerol(v/v)). The membrane suspension was frozen by liquid nitrogen and stored at −80 °C for further use. After thawing on ice, 50 µm fenofibrate was added to the solution and incubated at 4 °C for 2 h. For the solubilization of the membrane, an equal volume of the detergent (100 mm HEPES pH 7.5, 200 mm NaCl, 1.5% LMNG, 0.3% CHS) was mixed with the membrane suspension and incubated at 4 °C for 3 h. The mixture was centrifuged at 35 000 rpm for 30 min and the supernatant was collected and incubated with TALON resin overnight. The resin was loaded onto a gravity column and washed with 15 column volume (CV) of the washing buffer 1 (25 mm HEPES pH 7.5, 100 mm NaCl, 10% Glycerol, 0.1% LMNG/0.02% CHS, 30 mm imidazole) and 15 CV of the washing buffer 2 (25 mm HEPES pH 7.5, 100 mm NaCl, 10% Glycerol, 0.03% LMNG/0.006% CHS, 50 mm imidazole). Then the resin was eluted with 4 CV of the elution buffer (25 mm HEPES pH 7.5, 100 mm NaCl, 10% Glycerol, 0.01% LMNG/0.002% CHS, 250 mm imidazole, 50 µm fenofibrate). Finally, the CB1‐LgBiT protein was concentrated to ≈1 mg mL−1 for complex assembly.
Expression and Purification of miniGs/q and Nb35
The miniGs/q construct and purification procedure used in this study were modified from the previously described.[ 25 ] The miniGs/q gene was subcloned into pET14a vector and expressed in BL21(DE3) cells. The miniGs/q purification was performed by using Ni‐FF resin and further purified by using Superdex 75 Increase 10/300 GL column (Cytiva). Finally, the purified miniGs/q were concentrated to 16 mg mL−1 for use.
Human Gβ1 with the N‐terminal 6xHis tag and C‐terminal HiBiT, and human wild type Gγ2 with C68S mutation were subcloned into the pFastBac Dual vector. The baculovirus was generated according to Bac‐to‐Bac system, and infected insect sf9 cells to produce the biomass for purification. The infected cells were harvested after 48 h and lysed by hypotonic and ultrasonic. The Gβ1(HiBiT)γ2(C68S) dimer was purified by using immobilized metal ion affinity chromatography (IMAC) and cation exchange chromatography (Mono Q). The peak fractions were concentrated to 1 mg mL−1 for use.
The Nanobody 35 (Nb35) with a C‐terminal 6xHis tag was expressed and purified as previously described.[ 22 ] Briefly, Nb35 was expressed in BL21(DE3) cells and purified by using nickel affinity chromatography, followed by size‐exclusion chromatography using a Superdex 75 increase 10/300 GL column, and finally concentrated to 1 mg mL−1.
Assembly and Purification of CB1‐Fenofibrate‐miniGs/q‐Nb35 Complex
The purified CB1‐LgBiT, miniGs/q, Gβ1(HiBiT)γ2(C68S), and Nb35 were mixed in a molar ratio of 1:2:2:2 with the addition of 50 µm fenofibrate and incubated at 4 °Cfor overnight. The assembled complex was further purified in the buffer (20 mm HEPES pH 7.5, 100 mm NaCl, 0.00075% (w/v) LMNG, 0.00025% (w/v) CHS, 0.00025% (w/v) GDN, 100 µm TCEP, 50 µm fenofibrate) by Superdex 200 Increase 10/300 GL column (Cytiva). The fractions with the component molar ratio of 1:1:1:1 were collected and concentrated to 3 mg mL−1.
Cryo‐EM Sample Preparation and Data Collection
Three microliters of sample was applied to glow‐discharged holey carbon grid (Quantifoil 200 mesh, R1.2/1.3), and vitrified in liquid ethane using Vitrobot Mark IV (Thermo Fisher Scientific). The grid was blotted for 3 s with blot force −1 under chamber conditions of 100% humidity and 4 °C. The cryo‐EM movie stacks were collected on a Titan Krios microscope operated at 300 kV equipped with Gatan K3 summit direct electron camera and a Gatan energy filter (slit set to 20 eV). Data were recorded at a nominal magnification of 105000 in counting mode, corresponding to a magnified pixel size of 0.416 Å. The total dose is ≈60 e− Å−2, divided into 40 frames. Each point was exposed for 1.997s with the dose rate ≈20 e− Å−2 s−1. The defocus range was set from −0.8 to −2.0 in SerialEM software to collect 3347 movies for 3D reconstitution.
Cryo‐EM Data Processing
The movies were imported into RELION 4.0[ 28 ] and beam‐induced motion correction was performed with MotionCor2 [ 29 ] binning 2 to the physical pixel size of 0.832 Å. The corrected pictures were imported into CryoSPARC 3.2.0.[ 30 ] Patch CTF estimated and filtered pictures with CTF<3.5 Å. The remaining 2753 pictures were subjected to blob picking with a size range from 110 to 160 Å. After particles were extracted and 2D was classified, obvious GPCR‐miniGs/q complex 2D classes were chosen as templates for template picking. The resulting particles were extracted with box size of 320 Å and subjected to one round 2D classification. The unclear 2D classes were excluded from the further 3D classification. The remaining 956199 particles were first Ab‐initio reconstructed into five volume classes, and the particles from the best class were chosen to perform second round 3D classification. The final best volume was subjected to non‐uniform refinement and local refinement with a mask on receptor and G alpha ras domain in CryoSPARC.
Model Building and Refinement
The initial template of CB1 was from CB1‐AM841‐Gi structure (PDB:6KPG), and downstream G protein and Nb35 were from GPR139‐JNJ63533054‐miniGs/q structure (PDB:7VUH). Agonist coordinates and geometry restraints were generated using CCP4.acedrg.[ 31 ] The models were mutated using PyMOL (http://www.pymol.org/pymol) and then were rigidly fit into the EM density map using UCSF Chimera X.[ 32 ] After iterative model building between Coot[ 33 ] and Phenix.real_space_refinement,[ 34 ] a good‐looking pose was generated. Based on this pose, a composite map was generated by phenix.combine_focused_maps from global refine and local refine map alignments. The final model was subjected to refinement on the composite map using phenix.real_space_refine in Phenix. The model geometry was evaluated using Molprobity.[ 35 ] The map resolutions of global refinement and local refinement were calculated with gold‐standard FSChalfmap‐halfmap = 0.143 criteria.
MD Simulations
The fenofibrate‐bound CB1‐miniGs/q complex was used as model. The receptor and ligand were used for simulations. CHARMM‐GUI membrane builder[ 36 ] was used to generate the system. CB1 was encapsulated with a bilayer of around 100 POPC in each leaf. The TIP3P water model was filled with a height of 12.5 Å on both sides of the membrane along the z‐axis. The box dimension is ≈90 Å X 90 Å X 90 Å. NaCl (0.15 m) was used to neutralize charges. The protein was parameterized by CHARMM36m force field,[ 37 ] while a conserved disulfide bond between C257 and C264 was fixed. D1632.50 and D2133.49 were kept protonated to mimic proton transportation during the active state. The ligand fenofibrate was parameterized by Antechamber[ 38 ] and transferred to CHARMM‐suited format in CHARMM‐GUI. Minimization, equilibrium, and production runs were conducted in GROMACS‐2023[ 39 ] version. A reduced harmonic restraint strategy was imposed in minimization and equilibrium, which leverage weights down to zero. Minimized with a maximum of 5000 steps with the steepest descent until convergence on 1000 kJ mol−1 nm−1 maximum force tolerance. In the equilibrium process, 0.25 ns with v‐rescale thermostat and 1.625 ns with v‐rescale thermostat and c‐rescale barostat were performed. Production run was running for a total of 200 ns, a time step of 2 fs for integration and saving trajectory per 100 ps with Nose–Hoover thermostat and Parrinello–Rahman barostat. During all md integrators, LINCS algorithm was used to assign covalently bonded hydrogen. For non‐bonded interaction, a 10–12 Å switch range and 12 Å cutoff were assigned, and long‐range interaction was calculated by the Particle Mesh Ewald (PME) method.[ 40 ]
MD Analysis
The full trajectory was concatenated by gmx.trjconv and gmx.trjcat. Mdtraj.rmsd[ 41 ] and mdtraj.compute_distances were used to calculate RMSD and the distance between denoted atoms. GetContacts (https://getcontacts.github.io/) was used to calculate contact frequency.
Conflict of Interest
The authors declare no conflict of interest.
Supporting information
Acknowledgements
The authors acknowledge support from the National Key Research and Development Program of China (2019YFA0904100, 2021YFA0910802, 2019YFA0904002, 2020YFA0908503, 2020YFA0907701, 2019YFA0904200, 2021YFA0910202 and 2022YFA1304701), the National Natural Science Foundation of China (22121003, 21837005, 91953202, 22193023, 31971200 and 32027901), the Strategic Priority Research Program of Chinese Academy of Sciences (XDB37040203) and the CAS Project for Young Scientists in Basic Research (YSBR‐015 and YSBR‐072‐6). The authors thank J. Liu, N. Chen, S. Hu, L. Jiang, and Z. Fan from the Insect Cell Expression Core and P. Si, and X. Liu from the Mammalian Cell Expression Core for Biomass production. The cryo‐EM data were collected at the Bio‐Electron Microscopy Facility of ShanghaiTech University with the assistance of L. Wang, D. Liu, Q. Sun, and Z. Zhang. This research also got support from Protein Purification Core, Cloning, and Assays Cores of iHuman Institute.
Untitled section
Wang T., Tang W., Zhao Z., Zhao R., Lv Z., Guo X., Gu Q., Liu B., Lv H., Chen J., Zhang K., Li F., Wang J., Fenofibrate Recognition and Gq Protein Coupling Mechanisms of the Human Cannabinoid Receptor CB1. Adv. Sci. 2024, 11, 2306311. 10.1002/advs.202306311
Contributor Information
Fahui Li, Email: lifahui@moon.ibp.ac.cn.
Jiangyun Wang, Email: jwang@ibp.ac.cn.
Data Availability Statement
The structure model and associated cryo‐EM data have been deposited in the Protein Data Bank (PDB) with entry 8K8J and Electron Microscopy Data Bank (EMDB) with entry EMD‐36951 (composite map), EMD‐36952 (global refine map), EMD‐36953 (local refine map). The unaligned raw movies were also provided in the Electron Microscopy Public Image Archive (EMPIAR) with entry EMPIAR‐11642.
References
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Associated Data
Supplementary Materials
Data Availability Statement
The structure model and associated cryo‐EM data have been deposited in the Protein Data Bank (PDB) with entry 8K8J and Electron Microscopy Data Bank (EMDB) with entry EMD‐36951 (composite map), EMD‐36952 (global refine map), EMD‐36953 (local refine map). The unaligned raw movies were also provided in the Electron Microscopy Public Image Archive (EMPIAR) with entry EMPIAR‐11642.