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Yorodumi- EMDB-28830: ELIC with Propylamine in saposin nanodiscs with 2:1:1 POPC:POPE:POPG -
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Open data
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Basic information
| Entry | ![]() | |||||||||
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| Title | ELIC with Propylamine in saposin nanodiscs with 2:1:1 POPC:POPE:POPG | |||||||||
Map data | Propylamine bound Wild Type ELIC in 2:1:1 POPC: POPE: POPG in saposin | |||||||||
Sample |
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Keywords | ELIC / ion channel / pLGIC / Structural Protein / Membrane Protein / TRANSPORT PROTEIN | |||||||||
| Function / homology | Function and homology informationextracellular ligand-gated monoatomic ion channel activity / transmembrane signaling receptor activity / identical protein binding / membrane Similarity search - Function | |||||||||
| Biological species | Dickeya dadantii (bacteria) | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 3.28 Å | |||||||||
Authors | Dalal V / Arcario MJ / Petroff II JT / Deitzen NM / Tan BK / Brannigan G / Cheng WWL | |||||||||
| Funding support | United States, 1 items
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Citation | Journal: Nat Commun / Year: 2024Title: Lipid nanodisc scaffold and size alter the structure of a pentameric ligand-gated ion channel. Authors: Vikram Dalal / Mark J Arcario / John T Petroff / Brandon K Tan / Noah M Dietzen / Michael J Rau / James A J Fitzpatrick / Grace Brannigan / Wayland W L Cheng / ![]() Abstract: Lipid nanodiscs have become a standard tool for studying membrane proteins, including using single particle cryo-electron microscopy (cryo-EM). We find that reconstituting the pentameric ligand-gated ...Lipid nanodiscs have become a standard tool for studying membrane proteins, including using single particle cryo-electron microscopy (cryo-EM). We find that reconstituting the pentameric ligand-gated ion channel (pLGIC), Erwinia ligand-gated ion channel (ELIC), in different nanodiscs produces distinct structures by cryo-EM. The effect of the nanodisc on ELIC structure extends to the extracellular domain and agonist binding site. Additionally, molecular dynamic simulations indicate that nanodiscs of different size impact ELIC structure and that the nanodisc scaffold directly interacts with ELIC. These findings suggest that the nanodisc plays a crucial role in determining the structure of pLGICs, and that reconstitution of ion channels in larger nanodiscs may better approximate a lipid membrane environment. | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_28830.map.gz | 78.1 MB | EMDB map data format | |
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| Header (meta data) | emd-28830-v30.xml emd-28830.xml | 20.1 KB 20.1 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_28830_fsc.xml | 10 KB | Display | FSC data file |
| Images | emd_28830.png | 34.9 KB | ||
| Filedesc metadata | emd-28830.cif.gz | 6 KB | ||
| Others | emd_28830_additional_1.map.gz emd_28830_half_map_1.map.gz emd_28830_half_map_2.map.gz | 64.4 MB 65.1 MB 65.1 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-28830 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-28830 | HTTPS FTP |
-Validation report
| Summary document | emd_28830_validation.pdf.gz | 892.3 KB | Display | EMDB validaton report |
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| Full document | emd_28830_full_validation.pdf.gz | 891.9 KB | Display | |
| Data in XML | emd_28830_validation.xml.gz | 17.1 KB | Display | |
| Data in CIF | emd_28830_validation.cif.gz | 22.5 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-28830 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-28830 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 8f33MC ![]() 8f32C ![]() 8f34C ![]() 8f35C ![]() 8twvC ![]() 8twzC C: citing same article ( M: atomic model generated by this map |
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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_28830.map.gz / Format: CCP4 / Size: 83.7 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Annotation | Propylamine bound Wild Type ELIC in 2:1:1 POPC: POPE: POPG in saposin | ||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 0.657 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Additional map: Propylamine bound Wild Type ELIC in 2:1:1 POPC: POPE: POPG in saposin
| File | emd_28830_additional_1.map | ||||||||||||
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| Annotation | Propylamine bound Wild Type ELIC in 2:1:1 POPC: POPE: POPG in saposin | ||||||||||||
| Projections & Slices |
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| Density Histograms |
-Half map: Propylamine bound Wild Type ELIC in 2:1:1 POPC: POPE: POPG in saposin
| File | emd_28830_half_map_1.map | ||||||||||||
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| Annotation | Propylamine bound Wild Type ELIC in 2:1:1 POPC: POPE: POPG in saposin | ||||||||||||
| Projections & Slices |
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| Density Histograms |
-Half map: Propylamine bound Wild Type ELIC in 2:1:1 POPC: POPE: POPG in saposin
| File | emd_28830_half_map_2.map | ||||||||||||
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| Annotation | Propylamine bound Wild Type ELIC in 2:1:1 POPC: POPE: POPG in saposin | ||||||||||||
| Projections & Slices |
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| Density Histograms |
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Sample components
-Entire : ELIC with Propylamine in saposin nanodiscs with 2:1:1 POPC:POPE:POPG
| Entire | Name: ELIC with Propylamine in saposin nanodiscs with 2:1:1 POPC:POPE:POPG |
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| Components |
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-Supramolecule #1: ELIC with Propylamine in saposin nanodiscs with 2:1:1 POPC:POPE:POPG
| Supramolecule | Name: ELIC with Propylamine in saposin nanodiscs with 2:1:1 POPC:POPE:POPG type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1 |
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| Source (natural) | Organism: Dickeya dadantii (bacteria) |
-Macromolecule #1: Erwinia chrysanthemi ligand-gated ion channel
| Macromolecule | Name: Erwinia chrysanthemi ligand-gated ion channel / type: protein_or_peptide / ID: 1 / Number of copies: 5 / Enantiomer: LEVO |
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| Source (natural) | Organism: Dickeya dadantii (bacteria) |
| Molecular weight | Theoretical: 36.879 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: APADNAADAR PVDVSVSIFI NKIYGVNTLE QTYKVDGYIV AQWTGKPRKT PGDKPLIVEN TQIERWINNG LWVPALEFIN VVGSPDTGN KRLMLFPDGR VIYNARFLGS FSNDMDFRLF PFDRQQFVLE LEPFSYNNQQ LRFSDIQVYT ENIDNEEIDE W WIRGKAST ...String: APADNAADAR PVDVSVSIFI NKIYGVNTLE QTYKVDGYIV AQWTGKPRKT PGDKPLIVEN TQIERWINNG LWVPALEFIN VVGSPDTGN KRLMLFPDGR VIYNARFLGS FSNDMDFRLF PFDRQQFVLE LEPFSYNNQQ LRFSDIQVYT ENIDNEEIDE W WIRGKAST HISDIRYDHL SSVQPNQNEF SRITVRIDAV RNPSYYLWSF ILPLGLIIAA SWSVFWLESF SERLQTSFTL ML TVVAYAF YTSNILPRLP YTTVIDQMII AGYGSIFAAI LLIIFAHHRQ ANGVEDDLLI QRCRLAFPLG FLAIGCVLVI RGI TL UniProtKB: Gamma-aminobutyric-acid receptor subunit beta-1 |
-Macromolecule #2: 3-AMINOPROPANE
| Macromolecule | Name: 3-AMINOPROPANE / type: ligand / ID: 2 / Number of copies: 5 / Formula: 3CN |
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| Molecular weight | Theoretical: 59.11 Da |
| Chemical component information | ![]() ChemComp-3CN: |
-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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| Grid | Model: Quantifoil R2/2 / Material: COPPER / Mesh: 300 / Pretreatment - Type: PLASMA CLEANING / Pretreatment - Time: 60 sec. / Pretreatment - Atmosphere: OTHER / Pretreatment - Pressure: 9.332 kPa / Details: O2 27.5 sccm H2 6.4 sccm |
| Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 277 K / Instrument: FEI VITROBOT MARK IV / Details: Blot for 2 seconds before plunging. |
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Electron microscopy
| Microscope | FEI TITAN KRIOS |
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| Specialist optics | Spherical aberration corrector: Microscope was equipped with a Cs corrector |
| Image recording | Film or detector model: FEI FALCON IV (4k x 4k) / Digitization - Dimensions - Width: 4096 pixel / Digitization - Dimensions - Height: 4096 pixel / Number grids imaged: 1 / Average exposure time: 4.28 sec. / Average electron dose: 47.55 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | C2 aperture diameter: 50.0 µm / Calibrated magnification: 96000 / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 0.01 mm / Nominal defocus max: 2.4 µm / Nominal defocus min: 0.8 µm / Nominal magnification: 96000 |
| Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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Image processing
-Atomic model buiding 1
| Refinement | Space: REAL / Protocol: AB INITIO MODEL |
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| Output model | ![]() PDB-8f33: |
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About Yorodumi



Keywords
Dickeya dadantii (bacteria)
Authors
United States, 1 items
Citation












Z (Sec.)
Y (Row.)
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FIELD EMISSION GUN


