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Yorodumi- EMDB-41908: Local refinement map on VFT-CRD of active-state CaSR in lipid nan... -
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Basic information
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| Title | Local refinement map on VFT-CRD of active-state CaSR in lipid nanodiscs | |||||||||
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Keywords | Family C GPCR / Calcium-sensing Receptor (CaSR) / Cryo-EM / Lipid Nanodiscs / Positive Allosteric Modulator / Membrane Protein / SIGNALING PROTEIN | |||||||||
| Biological species | Homo sapiens (human) | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 2.6 Å | |||||||||
Authors | He F / Wu C / Gao Y / Skiniotis G | |||||||||
| Funding support | United States, 1 items
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Citation | Journal: Nature / Year: 2024Title: Allosteric modulation and G-protein selectivity of the Ca-sensing receptor. Authors: Feng He / Cheng-Guo Wu / Yang Gao / Sabrina N Rahman / Magda Zaoralová / Makaía M Papasergi-Scott / Ting-Jia Gu / Michael J Robertson / Alpay B Seven / Lingjun Li / Jesper M Mathiesen / Georgios Skiniotis / ![]() Abstract: The calcium-sensing receptor (CaSR) is a family C G-protein-coupled receptor (GPCR) that has a central role in regulating systemic calcium homeostasis. Here we use cryo-electron microscopy and ...The calcium-sensing receptor (CaSR) is a family C G-protein-coupled receptor (GPCR) that has a central role in regulating systemic calcium homeostasis. Here we use cryo-electron microscopy and functional assays to investigate the activation of human CaSR embedded in lipid nanodiscs and its coupling to functional G versus G proteins in the presence and absence of the calcimimetic drug cinacalcet. High-resolution structures show that both G and G drive additional conformational changes in the activated CaSR dimer to stabilize a more extensive asymmetric interface of the seven-transmembrane domain (7TM) that involves key protein-lipid interactions. Selective G and G coupling by the receptor is achieved through substantial rearrangements of intracellular loop 2 and the C terminus, which contribute differentially towards the binding of the two G-protein subtypes, resulting in distinct CaSR-G-protein interfaces. The structures also reveal that natural polyamines target multiple sites on CaSR to enhance receptor activation by zipping negatively charged regions between two protomers. Furthermore, we find that the amino acid L-tryptophan, a well-known ligand of CaSR extracellular domains, occupies the 7TM bundle of the G-protein-coupled protomer at the same location as cinacalcet and other allosteric modulators. Together, these results provide a framework for G-protein activation and selectivity by CaSR, as well as its allosteric modulation by endogenous and exogenous ligands. | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_41908.map.gz | 398.2 MB | EMDB map data format | |
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| Header (meta data) | emd-41908-v30.xml emd-41908.xml | 12.9 KB 12.9 KB | Display Display | EMDB header |
| Images | emd_41908.png | 87.1 KB | ||
| Filedesc metadata | emd-41908.cif.gz | 4 KB | ||
| Others | emd_41908_half_map_1.map.gz emd_41908_half_map_2.map.gz | 391.9 MB 391.9 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-41908 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-41908 | HTTPS FTP |
-Validation report
| Summary document | emd_41908_validation.pdf.gz | 1.2 MB | Display | EMDB validaton report |
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| Full document | emd_41908_full_validation.pdf.gz | 1.2 MB | Display | |
| Data in XML | emd_41908_validation.xml.gz | 18 KB | Display | |
| Data in CIF | emd_41908_validation.cif.gz | 21.2 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-41908 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-41908 | HTTPS FTP |
-Related structure data
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Map
| File | Download / File: emd_41908.map.gz / Format: CCP4 / Size: 421.9 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 0.8677 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Half map: #1
| File | emd_41908_half_map_1.map | ||||||||||||
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-Half map: #2
| File | emd_41908_half_map_2.map | ||||||||||||
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| Density Histograms |
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Sample components
-Entire : Cinacalcet-bound active-state human calcium-sensing receptor CaSR...
| Entire | Name: Cinacalcet-bound active-state human calcium-sensing receptor CaSR in lipid nanodiscs |
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| Components |
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-Supramolecule #1: Cinacalcet-bound active-state human calcium-sensing receptor CaSR...
| Supramolecule | Name: Cinacalcet-bound active-state human calcium-sensing receptor CaSR in lipid nanodiscs type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#4 |
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| Source (natural) | Organism: Homo sapiens (human) |
-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: 7.5 |
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| Vitrification | Cryogen name: ETHANE |
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Electron microscopy
| Microscope | FEI TITAN KRIOS |
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| Image recording | Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Average electron dose: 50.0 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 1.5 µm / Nominal defocus min: 0.5 µm |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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Image processing
| Startup model | Type of model: OTHER |
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| Final reconstruction | Resolution.type: BY AUTHOR / Resolution: 2.6 Å / Resolution method: FSC 0.143 CUT-OFF / Number images used: 234170 |
| Initial angle assignment | Type: MAXIMUM LIKELIHOOD |
| Final angle assignment | Type: MAXIMUM LIKELIHOOD |
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About Yorodumi



Keywords
Homo sapiens (human)
Authors
United States, 1 items
Citation























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FIELD EMISSION GUN
