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Open data
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Basic information
| Entry | Database: EMDB / ID: EMD-20508 | |||||||||
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| Title | MscS Nanodisc with N-terminal His-Tag | |||||||||
Map data | MscS ND with N-terminal His-Tag | |||||||||
Sample |
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Keywords | MscS / Nanodisc / Mechanosensitive Channel of Small Conductance / Mechanosensitive / Channel / MEMBRANE PROTEIN | |||||||||
| Function / homology | Function and homology informationintracellular water homeostasis / mechanosensitive monoatomic ion channel activity / protein homooligomerization / monoatomic ion transmembrane transport / identical protein binding / membrane / plasma membrane Similarity search - Function | |||||||||
| Biological species | ![]() ![]() | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 3.1 Å | |||||||||
Authors | Reddy BG / Perozo E | |||||||||
| Funding support | United States, 1 items
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Citation | Journal: Elife / Year: 2019Title: Molecular basis of force-from-lipids gating in the mechanosensitive channel MscS. Authors: Bharat Reddy / Navid Bavi / Allen Lu / Yeonwoo Park / Eduardo Perozo / ![]() Abstract: Prokaryotic mechanosensitive (MS) channels open by sensing the physical state of the membrane. As such, lipid-protein interactions represent the defining molecular process underlying ...Prokaryotic mechanosensitive (MS) channels open by sensing the physical state of the membrane. As such, lipid-protein interactions represent the defining molecular process underlying mechanotransduction. Here, we describe cryo-electron microscopy (cryo-EM) structures of the small-conductance mechanosensitive channel (MscS) in nanodiscs (ND). They reveal a novel membrane-anchoring fold that plays a significant role in channel activation and establish a new location for the lipid bilayer, shifted ~14 Å from previous consensus placements. Two types of lipid densities are explicitly observed. A phospholipid that 'hooks' the top of each TM2-TM3 hairpin and likely plays a role in force sensing, and a bundle of acyl chains occluding the permeation path above the L105 cuff. These observations reshape our understanding of force-from-lipids gating in MscS and highlight the key role of allosteric interactions between TM segments and phospholipids bound to key dynamic components of the channel. | |||||||||
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Structure visualization
| Movie |
Movie viewer |
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| Structure viewer | EM map: SurfView Molmil Jmol/JSmol |
| Supplemental images |
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Downloads & links
-EMDB archive
| Map data | emd_20508.map.gz | 49.1 MB | EMDB map data format | |
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| Header (meta data) | emd-20508-v30.xml emd-20508.xml | 18.7 KB 18.7 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_20508_fsc.xml | 10.6 KB | Display | FSC data file |
| Images | emd_20508.png | 121.6 KB | ||
| Filedesc metadata | emd-20508.cif.gz | 6.3 KB | ||
| Others | emd_20508_half_map_1.map.gz emd_20508_half_map_2.map.gz | 49.5 MB 49.7 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-20508 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-20508 | HTTPS FTP |
-Validation report
| Summary document | emd_20508_validation.pdf.gz | 723.1 KB | Display | EMDB validaton report |
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| Full document | emd_20508_full_validation.pdf.gz | 722.7 KB | Display | |
| Data in XML | emd_20508_validation.xml.gz | 15.9 KB | Display | |
| Data in CIF | emd_20508_validation.cif.gz | 21.1 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-20508 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-20508 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 6pwnMC ![]() 6pwoC ![]() 6pwpC C: citing same article ( M: atomic model generated by this map |
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| Similar structure data | |
| EM raw data | EMPIAR-10496 (Title: MscS Nanodisc with N-terminal His-Tag / Data size: 762.3 Data #1: MscS Nanodisc with N-terminal His-Tag [micrographs - multiframe]) |
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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_20508.map.gz / Format: CCP4 / Size: 64 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Annotation | MscS ND with N-terminal His-Tag | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 1.064 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
CCP4 map header:
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-Supplemental data
-Half map: Unfiltered Half Map 2
| File | emd_20508_half_map_1.map | ||||||||||||
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| Annotation | Unfiltered Half Map 2 | ||||||||||||
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| Density Histograms |
-Half map: Unfiltered Half Map 1
| File | emd_20508_half_map_2.map | ||||||||||||
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| Annotation | Unfiltered Half Map 1 | ||||||||||||
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Sample components
-Entire : Mechanosensitive Channel of Small Conductance
| Entire | Name: Mechanosensitive Channel of Small Conductance |
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| Components |
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-Supramolecule #1: Mechanosensitive Channel of Small Conductance
| Supramolecule | Name: Mechanosensitive Channel of Small Conductance / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1 |
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| Source (natural) | Organism: ![]() |
-Macromolecule #1: Small-conductance mechanosensitive channel
| Macromolecule | Name: Small-conductance mechanosensitive channel / type: protein_or_peptide / ID: 1 / Number of copies: 7 / Enantiomer: LEVO |
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| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 33.094258 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: MGSSHHHHHH SSGLVPRGSH MEDLNVVDSI NGAGSWLVAN QALLLSYAVN IVAALAIIIV GLIIARMISN AVNRLMISRK IDATVADFL SALVRYGIIA FTLIAALGRV GVQTASVIAV LGAAGLAVGL ALQGSLSNLA AGVLLVMFRP FRAGEYVDLG G VAGTVLSV ...String: MGSSHHHHHH SSGLVPRGSH MEDLNVVDSI NGAGSWLVAN QALLLSYAVN IVAALAIIIV GLIIARMISN AVNRLMISRK IDATVADFL SALVRYGIIA FTLIAALGRV GVQTASVIAV LGAAGLAVGL ALQGSLSNLA AGVLLVMFRP FRAGEYVDLG G VAGTVLSV QIFSTTMRTA DGKIIVIPNG KIIAGNIINF SREPVRRNEF IIGVAYDSDI DQVKQILTNI IQSEDRILKD RE MTVRLNE LGASSINFVV RVWSNSGDLQ NVYWDVLERI KREFDAAGIS FPYPQMDVNF KRVKEDKAA UniProtKB: Small-conductance mechanosensitive channel |
-Macromolecule #2: (2S)-3-(hexadecanoyloxy)-2-[(9Z)-octadec-9-enoyloxy]propyl 2-(tri...
| Macromolecule | Name: (2S)-3-(hexadecanoyloxy)-2-[(9Z)-octadec-9-enoyloxy]propyl 2-(trimethylammonio)ethyl phosphate type: ligand / ID: 2 / Number of copies: 7 / Formula: POV |
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| Molecular weight | Theoretical: 760.076 Da |
| Chemical component information | ![]() ChemComp-POV: |
-Macromolecule #3: HEXADECANE
| Macromolecule | Name: HEXADECANE / type: ligand / ID: 3 / Number of copies: 7 / Formula: R16 |
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| Molecular weight | Theoretical: 226.441 Da |
| Chemical component information | ![]() ChemComp-R16: |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Concentration | 2 mg/mL |
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| Buffer | pH: 7.4 |
| Grid | Model: Quantifoil R2/2 / Material: COPPER / Mesh: 200 / Pretreatment - Type: GLOW DISCHARGE |
| Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 295 K / Instrument: FEI VITROBOT MARK IV Details: 22C. Blot Force 3 for 3 seconds. Double application with a blotting between applications.. |
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Electron microscopy
| Microscope | FEI TITAN KRIOS |
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| Image recording | Film or detector model: GATAN K2 SUMMIT (4k x 4k) / Detector mode: COUNTING / 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 |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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Image processing
-Atomic model buiding 1
| Refinement | Space: REAL / Protocol: FLEXIBLE FIT |
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| Output model | ![]() PDB-6pwn: |
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Keywords
Authors
United States, 1 items
Citation
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