Neuropeptide Y (NPY) receptors belong to the G-protein-coupled receptor superfamily and have important roles in food intake, anxiety and cancer biology1,2. The NPY–Y receptor system has emerged as one of the most complex networks with three peptide ligands (NPY, peptide YY and pancreatic polypeptide) binding to four receptors in most mammals, namely the Y1, Y2, Y4 and Y5 receptors, with different affinity and selectivity3. NPY is the most powerful stimulant of food intake and this effect is primarily mediated by the Y1 receptor (Y1R)4. A number of peptides and small-molecule compounds have been characterized as Y1R antagonists and have shown clinical potential in the treatment of obesity4, tumour1 and bone loss5. However, their clinical usage has been hampered by low potency and selectivity, poor brain penetration ability or lack of oral bioavailability6. Here we report crystal structures of the human Y1R bound to the two selective antagonists UR-MK299 and BMS-193885 at 2.7 and 3.0 Å resolution, respectively. The structures combined with mutagenesis studies reveal the binding modes of Y1R to several structurally diverse antagonists and the determinants of ligand selectivity. The Y1R structure and molecular docking of the endogenous agonist NPY, together with nuclear magnetic resonance, photo-crosslinking and functional studies, provide insights into the binding behaviour of the agonist and for the first time, to our knowledge, determine the interaction of its N terminus with the receptor. These insights into Y1R can enable structure-based drug discovery that targets NPY receptors.
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We are grateful to T. Zellmann for his contribution to the modelling in the early state of the project and for the technical support of R. Reppich-Sacher (mass spectrometry) and K. Löbner (cell culture). We thank H. A. Scheidt for support with solid-state NMR measurements and M. Beer-Krön, D. Fritsch, S. Bollwein and B. Wenzl for expert help in performing radioligand-binding experiments. The synchrotron radiation experiments were performed at the BL41XU of SPring-8 with approval of the Japan Synchrotron Radiation Research Institute (proposal no. 2015B2026, 2015B2027, 2016A2517, 2016A2518, 2016B2517 and 2016B2518). We thank the beamline staff members K. Hasegawa, H. Okumura, N. Mizuno, T. Kawamura and H. Murakami of the BL41XU for help with X-ray data collection. This work was supported by CAS Strategic Priority Research Programs XDB08020000 (B.W.) and XDB08030102 (R.Z.), the Key Research Program of Frontier Sciences, CAS, Grant no. QYZDB-SSW-SMC024 (B.W.) and QYZDB-SSW-SMC054 (Q.Z.), the National Science Foundation of China grants 31570739 (B.W.), 81525024 (Q.Z.), 3170040264 (Z.Y.) and 31470792 (S.Y.), Program of Shanghai Academic/Technology Research Leader no. 18XD1404800 (Z.Y., Q.Z.), the European Community, the Free State of Saxony (SAB 100148835 to D.H. and 100881433 to A.G.B.-S.) and the Deutsche Forschungsgemeinschaft (DFG) (Be1264-16, SFB 1052/A3, research grant KE 1857/1-1 and Graduate Training Program GRK 1910). Work in the Meiler laboratory is supported by the NIH (R01 GM080403, R01 DK097376, R01 HL122010) and NSF (CHE 1305874).
Nature thanks N. Holliday and the other anonymous reviewer(s) for their contribution to the peer review of this work.
Extended data figures and tables
Extended Data Fig. 1 Crystal packing and structural features of Y1R and chemical structures of Y1R ligands.
a, b, Crystal packing of Y1R–UR-MK299 (a) and Y1R–BMS-193885 (b) complexes. Y1R is shown in cartoon representation and coloured brown and green in the Y1R–UR-MK299 and Y1R–BMS-193885 complexes, respectively. The T4L fusion is shown in grey cartoon representation. UR-MK299 and BMS-193885 are displayed as yellow and pink spheres, respectively. c, Cutaway view of the UR-MK299-binding pocket in Y1R. The receptor is shown in brown cartoon and surface representations. The ligand is shown as yellow sticks. d, Comparison of Y1R in the Y1R–UR-MK299 crystal structure (brown) and the Y1R–NPY model (green). Side chains of Q1203.32 and W2766.48 are shown as sticks. R35–Y36 of NPY is displayed as cyan sticks. The hydrogen bond between Q1203.32 and Y36 of NPY is shown as a green dashed line. e–j, Chemical structures of the argininamide Y1R antagonists BIBP3226 (e), UR-HU404 (f), UR-MK299 (g), BIBO3304 (h), UR-MK289 (i) and UR-MK136 (j). k, Chemical structure of BMS-193885. l, Scaffold of NPY C-terminal residues R35 and Y36. Key differences between R35–Y36 of NPY and UR-MK299 are chirality of the arginine derivative and alteration of bond connectivity leading to the hydroxyphenyl group.
Extended Data Fig. 2 Expression of wild-type and mutant Y1 receptors in transiently transfected COS-7 cells.
a, Live-cell fluorescence microscopy verifies all Y1R variants to be properly folded and exported to the cell membrane like the wild-type receptor. Nuclei stained with Hoechst33342. Scale bars, 10 μm. Pictures are representative of two independent experiments with similar results. b, The total expression level was determined by fluorescence reading and expression was confirmed to be similar to the wild type. Transfection of only 50% or 25% of the DNA amount (with total DNA amount held constant by empty vector), led to a proportional decrease of fluorescence, and thus, expression level. Data represent mean ± s.e.m. of three to five independent experiments performed in technical triplicate (see Source Data for sample size of each mutant). c, Estimation of the receptor reserve in functional inositol phosphate accumulation assays. Transfection of half of the vector encoding the receptor (with a constant total DNA amount including chimeric G protein, see a) still produces maximum signal, while further reduction results in signal loss at comparable potency. Thus, there is only a small receptor reserve in the functional readout, allowing potency alteration to be directly related to compromised ligand binding. Data represent mean ± s.e.m. of three independent experiments performed in technical duplicate. cNPY, concentration of NPY. Source data
Colours represent the similarity of residues: red background, identical; red text, strongly similar. Key residues in the UR-MK299-binding pocket, which are conserved or variable among receptors, are indicated by red or black arrows, respectively. The alignment was generated using UniProt (http://www.uniprot.org/align/) and the graphic was prepared on the ESPript 3.0 server (http://espript.ibcp.fr/ESPript/cgi-bin/ESPript.cgi).
Extended Data Fig. 4 Pharmacological characterization of refolded Y1R and NMR studies of Y1R-bound NPY.
a, Binding of Atto 520-labelled NPY (50 nM) to increasing amounts of bicelles containing Y1R or empty bicelles. Data reflect fluorescence enhancement upon binding. An inflection point at EC50 = 52 nM was determined. Two independent experiments were performed in technical duplicate with similar results. Data shown are from a representative experiment. a.u., arbitrary units. c(Y1R), concentration of Y1R. b, Typical 13C MAS single-quantum (SQ)/double-quantum (DQ) correlation spectrum of NPY in the presence of Y1R reconstituted into large bicelles at −30 °C. NMR spectra were acquired from one to three independent preparations for each labelled amino acid with similar results (see d). Data shown are from a representative experiment. c, Table showing 13C-NMR chemical shifts of assigned amino acids of NPY bound to Y1R (referenced to tetramethylsilane) as acquired in solid-state NMR experiments. d, 13C-chemical-shift index of NPY bound to Y1R in large DMPC/DHPC-c7 bicelles (q > 20) compared with docked models. Plotted in black is the measured chemical shift difference (Cα − Cβ) for each individual residue of NPY minus the chemical shift difference of the same amino acid type in random-coil conformation. Individual data points from one to three independent experiments for each labelled amino acid are shown. Typical experimental error when determining chemical shifts under these conditions are ± 1 p.p.m. Chemical shifts were back-calculated for the top docking solutions and filtered against the experimental data to generate a final ensemble of docked poses. Their average chemical-shift index and associated s.d. from the top ten docked poses are shown in red.
a, Mass spectra of photo-crosslinked Y1R with [Bpa1, K4[(Ahx)2-biotin]]NPY. Exemplary MALDI–TOF mass spectra of photo-crosslinked samples enzymatically digested by rLys-C and Glu-C. Potential Y1R fragments are labelled. Two independent experiments were performed with similar results. N, N terminus of Y1R (blue); E, ECL2 (red). b, Respective regions of NPY N terminus at Y1R. Amino acid sequence of Y1R with a C-terminal His-tag. The two detected regions within Y1R (N terminus (blue), ECL2 (red)) after crosslinking with [Bpa1,K4[(Ahx)2-biotin]]NPY are emphasized in boxes. The different sizes of the boxes represent different detected fragments (Extended Data Table 5). Experiments were repeated twice independently with similar results, and only fragments that were observed in both experiments are listed here and in Extended Data Table 5. c, Binding of Atto 520-labelled NPY (50 nM) to increasing amounts of cell-free produced Y1R in Brij-58. Data reflect fluorescence enhancement upon binding. An EC50 value of 69 nM was determined. Data shown are mean ± s.e.m. from six independent experiments performed in technical triplicate. c(Y1R), concentration of Y1R. Source data
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Radiosynthesis and in vivo evaluation of 11C-labeled BMS-193885 and its desmethyl analog as PET tracers for neuropeptide Y1 receptors
EJNMMI Radiopharmacy and Chemistry (2019)
Nature Communications (2019)
Nature Reviews Drug Discovery (2018)