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Yorodumi- EMDB-47493: Cryo-EM structure of the human P2X7 receptor in the UB-MBX-46-bou... -
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Basic information
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| Title | Cryo-EM structure of the human P2X7 receptor in the UB-MBX-46-bound inhibited state | |||||||||
Map data | Sharpened map for human P2X7 in the UB-MBX-46-bound inhibited state | |||||||||
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Keywords | Membrane Protein / Ion Channel / Ligand-Gated Ion Channel / P2X Receptor / P2XR / Allosteric Antagonist / Agonist | |||||||||
| Function / homology | Function and homology informationpositive regulation of bleb assembly / NAD transport / gamma-aminobutyric acid secretion / phagolysosome assembly / phospholipid transfer to membrane / positive regulation of cytoskeleton organization / Platelet homeostasis / positive regulation of monoatomic ion transmembrane transport / purinergic nucleotide receptor signaling pathway / extracellularly ATP-gated monoatomic cation channel activity ...positive regulation of bleb assembly / NAD transport / gamma-aminobutyric acid secretion / phagolysosome assembly / phospholipid transfer to membrane / positive regulation of cytoskeleton organization / Platelet homeostasis / positive regulation of monoatomic ion transmembrane transport / purinergic nucleotide receptor signaling pathway / extracellularly ATP-gated monoatomic cation channel activity / positive regulation of gamma-aminobutyric acid secretion / positive regulation of interleukin-1 alpha production / purinergic nucleotide receptor activity / collagen metabolic process / positive regulation of prostaglandin secretion / pore complex assembly / negative regulation of cell volume / T cell apoptotic process / plasma membrane phospholipid scrambling / mitochondrial depolarization / Elevation of cytosolic Ca2+ levels / bleb assembly / vesicle budding from membrane / positive regulation of T cell apoptotic process / prostaglandin secretion / bleb / response to fluid shear stress / glutamate secretion / cellular response to dsRNA / negative regulation of bone resorption / ceramide biosynthetic process / skeletal system morphogenesis / positive regulation of macrophage cytokine production / positive regulation of glutamate secretion / Mechanical load activates signaling by PIEZO1 and integrins in osteocytes / response to zinc ion / sodium channel activity / protein homotrimerization / response to ATP / cellular response to ATP / positive regulation of NLRP3 inflammasome complex assembly / positive regulation of mitochondrial depolarization / T cell homeostasis / membrane protein ectodomain proteolysis / The NLRP3 inflammasome / protein secretion / synaptic vesicle exocytosis / response to electrical stimulus / positive regulation of calcium ion transport into cytosol / membrane depolarization / T cell proliferation / positive regulation of bone mineralization / potassium channel activity / response to mechanical stimulus / Purinergic signaling in leishmaniasis infection / regulation of sodium ion transport / extrinsic apoptotic signaling pathway / negative regulation of MAPK cascade / release of sequestered calcium ion into cytosol / reactive oxygen species metabolic process / homeostasis of number of cells within a tissue / sensory perception of pain / positive regulation of glycolytic process / response to ischemia / positive regulation of protein secretion / positive regulation of interleukin-1 beta production / T cell mediated cytotoxicity / protein catabolic process / apoptotic signaling pathway / neuromuscular junction / mitochondrion organization / calcium-mediated signaling / lipopolysaccharide binding / protein processing / response to calcium ion / positive regulation of interleukin-6 production / positive regulation of T cell mediated cytotoxicity / calcium ion transmembrane transport / cell morphogenesis / cell-cell junction / MAPK cascade / presynapse / response to lipopolysaccharide / positive regulation of MAPK cascade / cell surface receptor signaling pathway / postsynapse / defense response to Gram-positive bacterium / response to xenobiotic stimulus / inflammatory response / signaling receptor binding / external side of plasma membrane / neuronal cell body / positive regulation of gene expression / GTP binding / mitochondrion / ATP binding / membrane / metal ion binding / identical protein binding / plasma membrane Similarity search - Function | |||||||||
| Biological species | Homo sapiens (human) | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 2.53 Å | |||||||||
Authors | Oken AC / Turcu AL / Vazquez S / Mansoor SE | |||||||||
| Funding support | United States, 2 items
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Citation | Journal: Nat Commun / Year: 2025Title: A polycyclic scaffold identified by structure-based drug design effectively inhibits the human P2X7 receptor. Authors: Adam C Oken / Andreea L Turcu / Eva Tzortzini / Kyriakos Georgiou / Jessica Nagel / Franka G Westermann / Marta Barniol-Xicota / Jonas Seidler / Ga-Ram Kim / So-Deok Lee / Annette Nicke / ...Authors: Adam C Oken / Andreea L Turcu / Eva Tzortzini / Kyriakos Georgiou / Jessica Nagel / Franka G Westermann / Marta Barniol-Xicota / Jonas Seidler / Ga-Ram Kim / So-Deok Lee / Annette Nicke / Yong-Chul Kim / Christa E Müller / Antonios Kolocouris / Santiago Vázquez / Steven E Mansoor / ![]() Abstract: The P2X7 receptor is an ATP-gated ion channel that activates inflammatory pathways involved in diseases such as cancer, atherosclerosis, and neurodegeneration. However, despite the potential benefits ...The P2X7 receptor is an ATP-gated ion channel that activates inflammatory pathways involved in diseases such as cancer, atherosclerosis, and neurodegeneration. However, despite the potential benefits of blocking overactive signaling, no P2X7 receptor antagonists have been approved for clinical use. Understanding species-specific pharmacological effects of existing antagonists has been challenging, in part due to the dearth of molecular information on receptor orthologs. Here, to identify distinct molecular features in the human receptor, we determine high-resolution cryo-EM structures of the full-length wild-type human P2X7 receptor in apo closed and ATP-bound open state conformations and draw comparisons with structures of other orthologs. We also report a cryo-EM structure of the human receptor in complex with an adamantane-based inhibitor, which we leverage, in conjunction with functional data and molecular dynamics simulations, to design a potent and selective antagonist with a unique polycyclic scaffold. Functional and structural analysis reveal how this optimized ligand, termed UB-MBX-46, interacts with the classical allosteric pocket of the human P2X7 receptor with subnanomolar potency and high selectivity, revealing its significant therapeutic potential. | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_47493.map.gz | 736.1 MB | EMDB map data format | |
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| Header (meta data) | emd-47493-v30.xml emd-47493.xml | 21.9 KB 21.9 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_47493_fsc.xml | 22.4 KB | Display | FSC data file |
| Images | emd_47493.png | 103.6 KB | ||
| Masks | emd_47493_msk_1.map | 824 MB | Mask map | |
| Filedesc metadata | emd-47493.cif.gz | 6.8 KB | ||
| Others | emd_47493_additional_1.map.gz emd_47493_half_map_1.map.gz emd_47493_half_map_2.map.gz | 396.5 MB 723.1 MB 723.1 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-47493 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-47493 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 9e3pMC ![]() 9e3mC ![]() 9e3nC ![]() 9e3oC ![]() 9e3qC M: atomic model generated by this map C: citing same article ( |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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| Related items in Molecule of the Month |
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Map
| File | Download / File: emd_47493.map.gz / Format: CCP4 / Size: 824 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Annotation | Sharpened map for human P2X7 in the UB-MBX-46-bound inhibited state | ||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 0.648 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Mask #1
| File | emd_47493_msk_1.map | ||||||||||||
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| Density Histograms |
-Additional map: Unsharpened map for human P2X7 in the UB-MBX-46-bound inhibited state
| File | emd_47493_additional_1.map | ||||||||||||
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| Annotation | Unsharpened map for human P2X7 in the UB-MBX-46-bound inhibited state | ||||||||||||
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| Density Histograms |
-Half map: Half map A for human P2X7 in the UB-MBX-46-bound inhibited state
| File | emd_47493_half_map_1.map | ||||||||||||
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| Annotation | Half map A for human P2X7 in the UB-MBX-46-bound inhibited state | ||||||||||||
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| Density Histograms |
-Half map: Half map B for human P2X7 in the UB-MBX-46-bound inhibited state
| File | emd_47493_half_map_2.map | ||||||||||||
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| Annotation | Half map B for human P2X7 in the UB-MBX-46-bound inhibited state | ||||||||||||
| Projections & Slices |
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| Density Histograms |
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Sample components
+Entire : Membrane protein
+Supramolecule #1: Membrane protein
+Macromolecule #1: P2X purinoceptor 7
+Macromolecule #3: (1s,3R,4R,6r,8S,9S)-N'-(2-chlorophenyl)-3,4,8,9-tetramethyltetrac...
+Macromolecule #4: GUANOSINE-5'-DIPHOSPHATE
+Macromolecule #5: ZINC ION
+Macromolecule #6: 2-acetamido-2-deoxy-beta-D-glucopyranose
+Macromolecule #7: CHOLESTEROL HEMISUCCINATE
+Macromolecule #8: PALMITIC ACID
+Macromolecule #9: SODIUM ION
+Macromolecule #10: water
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Buffer | pH: 7 |
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| Vitrification | Cryogen name: ETHANE / Instrument: FEI VITROBOT MARK IV |
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Electron microscopy
| Microscope | FEI TITAN KRIOS |
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| Specialist optics | Energy filter - Slit width: 20 eV |
| Image recording | Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Number real images: 24191 / Average electron dose: 42.0 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | C2 aperture diameter: 50.0 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 1.4000000000000001 µm / Nominal defocus min: 0.9 µm / Nominal magnification: 130000 |
| Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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About Yorodumi



Keywords
Homo sapiens (human)
Authors
United States, 2 items
Citation


















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Processing
FIELD EMISSION GUN


