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Yorodumi- EMDB-42733: Constituent EM map: Focused refinement RY1&2 of the Structure of ... -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-42733 | |||||||||
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Title | Constituent EM map: Focused refinement RY1&2 of the Structure of PKA phosphorylated human RyR2-R420W in the primed state in the presence of calcium | |||||||||
Map data | Constituent EM map: Focused refinement RY1&2 of the Structure of PKA phosphorylated human RyR2-R420W in the primed state in the presence of calcium | |||||||||
Sample |
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Keywords | calcium channel / MEMBRANE PROTEIN | |||||||||
Biological species | Homo sapiens (human) | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 3.79 Å | |||||||||
Authors | Miotto MC / Marks AR | |||||||||
Funding support | United States, 1 items
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Citation | Journal: Nat Commun / Year: 2024 Title: Structural basis for ryanodine receptor type 2 leak in heart failure and arrhythmogenic disorders. Authors: Marco C Miotto / Steven Reiken / Anetta Wronska / Qi Yuan / Haikel Dridi / Yang Liu / Gunnar Weninger / Carl Tchagou / Andrew R Marks / Abstract: Heart failure, the leading cause of mortality and morbidity in the developed world, is characterized by cardiac ryanodine receptor 2 channels that are hyperphosphorylated, oxidized, and depleted of ...Heart failure, the leading cause of mortality and morbidity in the developed world, is characterized by cardiac ryanodine receptor 2 channels that are hyperphosphorylated, oxidized, and depleted of the stabilizing subunit calstabin-2. This results in a diastolic sarcoplasmic reticulum Ca leak that impairs cardiac contractility and triggers arrhythmias. Genetic mutations in ryanodine receptor 2 can also cause Ca leak, leading to arrhythmias and sudden cardiac death. Here, we solved the cryogenic electron microscopy structures of ryanodine receptor 2 variants linked either to heart failure or inherited sudden cardiac death. All are in the primed state, part way between closed and open. Binding of Rycal drugs to ryanodine receptor 2 channels reverts the primed state back towards the closed state, decreasing Ca leak, improving cardiac function, and preventing arrhythmias. We propose a structural-physiological mechanism whereby the ryanodine receptor 2 channel primed state underlies the arrhythmias in heart failure and arrhythmogenic disorders. | |||||||||
History |
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-Structure visualization
Supplemental images |
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-Downloads & links
-EMDB archive
Map data | emd_42733.map.gz | 247.3 MB | EMDB map data format | |
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Header (meta data) | emd-42733-v30.xml emd-42733.xml | 17.1 KB 17.1 KB | Display Display | EMDB header |
Images | emd_42733.png | 13.8 KB | ||
Filedesc metadata | emd-42733.cif.gz | 4.6 KB | ||
Others | emd_42733_half_map_1.map.gz emd_42733_half_map_2.map.gz | 473.9 MB 473.9 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-42733 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-42733 | HTTPS FTP |
-Validation report
Summary document | emd_42733_validation.pdf.gz | 908.4 KB | Display | EMDB validaton report |
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Full document | emd_42733_full_validation.pdf.gz | 907.9 KB | Display | |
Data in XML | emd_42733_validation.xml.gz | 18.6 KB | Display | |
Data in CIF | emd_42733_validation.cif.gz | 22.2 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-42733 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-42733 | HTTPS FTP |
-Related structure data
Related structure data | 8uq2C 8uq3C 8uq4C 8uq5C 8uxcC 8uxeC 8uxfC 8uxgC 8uxhC 8uxiC 8uxlC 8uxmC C: citing same article (ref.) |
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-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_42733.map.gz / Format: CCP4 / Size: 512 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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Annotation | Constituent EM map: Focused refinement RY1&2 of the Structure of PKA phosphorylated human RyR2-R420W in the primed state in the presence of calcium | ||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 0.83 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Half map: #1
File | emd_42733_half_map_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Sample components
-Entire : Complex of RyR2-R420W and Calstabin-2
Entire | Name: Complex of RyR2-R420W and Calstabin-2 |
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Components |
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-Supramolecule #1: Complex of RyR2-R420W and Calstabin-2
Supramolecule | Name: Complex of RyR2-R420W and Calstabin-2 / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#2 |
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-Supramolecule #2: Ryanodine Receptor 2
Supramolecule | Name: Ryanodine Receptor 2 / type: complex / ID: 2 / Parent: 1 / Macromolecule list: #1 |
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Source (natural) | Organism: Homo sapiens (human) |
-Supramolecule #3: Peptidyl- cis-trans isomerase FKBP1B
Supramolecule | Name: Peptidyl- cis-trans isomerase FKBP1B / type: complex / ID: 3 / Parent: 1 / Macromolecule list: #2 |
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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 |
-Sample preparation
Concentration | 2.5 mg/mL | |||||||||||||||||||||||||||
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Buffer | pH: 7.4 Component:
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Vitrification | Cryogen name: ETHANE |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Temperature | Min: 80.0 K / Max: 100.0 K |
Specialist optics | Energy filter - Name: GIF Bioquantum / Energy filter - Slit width: 20 eV |
Image recording | Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Digitization - Dimensions - Width: 5760 pixel / Digitization - Dimensions - Height: 4092 pixel / Average electron dose: 58.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | C2 aperture diameter: 100.0 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 1.2 µm / Nominal defocus min: 0.5 µm |
Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
-Image processing
Startup model | Type of model: INSILICO MODEL / In silico model: CryoSPARC ab initio |
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Final reconstruction | Resolution.type: BY AUTHOR / Resolution: 3.79 Å / Resolution method: FSC 0.143 CUT-OFF / Software - Name: cryoSPARC / Number images used: 223544 |
Initial angle assignment | Type: MAXIMUM LIKELIHOOD / Software - Name: cryoSPARC |
Final angle assignment | Type: MAXIMUM LIKELIHOOD |
-Atomic model buiding 1
Initial model | PDB ID: Chain - Source name: PDB / Chain - Initial model type: experimental model |
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