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Yorodumi- EMDB-9231: Cryo-EM structure of membrane-bound Synaptotagmin 1 C2AB domains ... -
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-Basic information
Entry | Database: EMDB / ID: EMD-9231 | |||||||||
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Title | Cryo-EM structure of membrane-bound Synaptotagmin 1 C2AB domains in a complex with the SNAREpin assembly in presence of Mg2+ | |||||||||
Map data | Cryo-EM map of Syt1-C2AB-SNAREpin complexes on the surface of negatively charged lipid nanotube flipped along z-axis. 10.4A resolution. | |||||||||
Sample |
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Function / homology | Function and homology information trans-Golgi Network Vesicle Budding / BLOC-1 complex / regulation of delayed rectifier potassium channel activity / myosin head/neck binding / synchronous neurotransmitter secretion / fast, calcium ion-dependent exocytosis of neurotransmitter / positive regulation of calcium ion-dependent exocytosis of neurotransmitter / syntaxin-3 binding / exocytic insertion of neurotransmitter receptor to postsynaptic membrane / Other interleukin signaling ...trans-Golgi Network Vesicle Budding / BLOC-1 complex / regulation of delayed rectifier potassium channel activity / myosin head/neck binding / synchronous neurotransmitter secretion / fast, calcium ion-dependent exocytosis of neurotransmitter / positive regulation of calcium ion-dependent exocytosis of neurotransmitter / syntaxin-3 binding / exocytic insertion of neurotransmitter receptor to postsynaptic membrane / Other interleukin signaling / calcium-dependent activation of synaptic vesicle fusion / synaptobrevin 2-SNAP-25-syntaxin-1a-complexin II complex / synaptobrevin 2-SNAP-25-syntaxin-1a complex / extrinsic component of presynaptic membrane / regulation of regulated secretory pathway / synaptic vesicle fusion to presynaptic active zone membrane / synaptobrevin 2-SNAP-25-syntaxin-1a-complexin I complex / spontaneous neurotransmitter secretion / Lysosome Vesicle Biogenesis / positive regulation of norepinephrine secretion / Glutamate Neurotransmitter Release Cycle / Norepinephrine Neurotransmitter Release Cycle / positive regulation of catecholamine secretion / Acetylcholine Neurotransmitter Release Cycle / Serotonin Neurotransmitter Release Cycle / GABA synthesis, release, reuptake and degradation / positive regulation of vesicle fusion / chromaffin granule membrane / Dopamine Neurotransmitter Release Cycle / Golgi Associated Vesicle Biogenesis / zymogen granule membrane / dense core granule / regulated exocytosis / ribbon synapse / presynaptic dense core vesicle exocytosis / synaptic vesicle docking / regulation of synaptic vesicle priming / regulation of calcium ion-dependent exocytosis / calcium ion sensor activity / storage vacuole / regulation of establishment of protein localization / response to gravity / vesicle-mediated transport in synapse / positive regulation of calcium ion-dependent exocytosis / Insertion of tail-anchored proteins into the endoplasmic reticulum membrane / calcium ion-regulated exocytosis of neurotransmitter / vesicle fusion / eosinophil degranulation / vesicle docking / exocytic vesicle / chloride channel inhibitor activity / secretion by cell / SNARE complex / SNAP receptor activity / positive regulation of dopamine secretion / protein heterooligomerization / Cargo recognition for clathrin-mediated endocytosis / regulation of exocytosis / regulation of vesicle-mediated transport / Clathrin-mediated endocytosis / LGI-ADAM interactions / calcium-ion regulated exocytosis / hormone secretion / actomyosin / positive regulation of intracellular protein transport / Golgi to plasma membrane protein transport / positive regulation of dendrite extension / neurotransmitter secretion / positive regulation of hormone secretion / neurotransmitter receptor internalization / calcium-dependent phospholipid binding / protein localization to membrane / ATP-dependent protein binding / neuron projection terminus / presynaptic cytosol / regulation of synaptic vesicle recycling / insulin secretion / syntaxin binding / neurotransmitter transport / syntaxin-1 binding / clathrin-coated vesicle / low-density lipoprotein particle receptor binding / SNARE complex assembly / positive regulation of neurotransmitter secretion / Neutrophil degranulation / endosomal transport / regulation of synaptic vesicle exocytosis / synaptic vesicle priming / regulation of synapse assembly / clathrin binding / postsynaptic cytosol / myosin binding / regulation of dopamine secretion / regulation of neuron projection development / phosphatidylserine binding / positive regulation of exocytosis / presynaptic active zone / modulation of excitatory postsynaptic potential / associative learning / exocytosis Similarity search - Function | |||||||||
Biological species | Rattus norvegicus (Norway rat) | |||||||||
Method | helical reconstruction / cryo EM / Resolution: 10.4 Å | |||||||||
Authors | Grushin K / Wang J / Coleman J / Rothman J / Sindelar C / Krishnakumar S | |||||||||
Funding support | United States, 1 items
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Citation | Journal: Nat Commun / Year: 2019 Title: Structural basis for the clamping and Ca activation of SNARE-mediated fusion by synaptotagmin. Authors: Kirill Grushin / Jing Wang / Jeff Coleman / James E Rothman / Charles V Sindelar / Shyam S Krishnakumar / Abstract: Synapotagmin-1 (Syt1) interacts with both SNARE proteins and lipid membranes to synchronize neurotransmitter release to calcium (Ca) influx. Here we report the cryo-electron microscopy structure of ...Synapotagmin-1 (Syt1) interacts with both SNARE proteins and lipid membranes to synchronize neurotransmitter release to calcium (Ca) influx. Here we report the cryo-electron microscopy structure of the Syt1-SNARE complex on anionic-lipid containing membranes. Under resting conditions, the Syt1 C2 domains bind the membrane with a magnesium (Mg)-mediated partial insertion of the aliphatic loops, alongside weak interactions with the anionic lipid headgroups. The C2B domain concurrently interacts the SNARE bundle via the 'primary' interface and is positioned between the SNAREpins and the membrane. In this configuration, Syt1 is projected to sterically delay the complete assembly of the associated SNAREpins and thus, contribute to clamping fusion. This Syt1-SNARE organization is disrupted upon Ca-influx as Syt1 reorients into the membrane, likely displacing the attached SNAREpins and reversing the fusion clamp. We thus conclude that the cation (Mg/Ca) dependent membrane interaction is a key determinant of the dual clamp/activator function of Synaptotagmin-1. | |||||||||
History |
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-Structure visualization
Movie |
Movie viewer |
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Structure viewer | EM map: SurfViewMolmilJmol/JSmol |
Supplemental images |
-Downloads & links
-EMDB archive
Map data | emd_9231.map.gz | 255.1 MB | EMDB map data format | |
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Header (meta data) | emd-9231-v30.xml emd-9231.xml | 15.8 KB 15.8 KB | Display Display | EMDB header |
FSC (resolution estimation) | emd_9231_fsc.xml | 14.6 KB | Display | FSC data file |
Images | emd_9231.png | 80.6 KB | ||
Masks | emd_9231_msk_1.map | 282.6 MB | Mask map | |
Others | emd_9231_half_map_1.map.gz emd_9231_half_map_2.map.gz | 224.6 MB 224.6 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-9231 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-9231 | HTTPS FTP |
-Validation report
Summary document | emd_9231_validation.pdf.gz | 690.3 KB | Display | EMDB validaton report |
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Full document | emd_9231_full_validation.pdf.gz | 689.9 KB | Display | |
Data in XML | emd_9231_validation.xml.gz | 20.1 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-9231 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-9231 | HTTPS FTP |
-Related structure data
Related structure data | 6mtiMC M: atomic model generated by this map C: citing same article (ref.) |
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Similar structure data |
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Related items in Molecule of the Month |
-Map
File | Download / File: emd_9231.map.gz / Format: CCP4 / Size: 282.6 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Annotation | Cryo-EM map of Syt1-C2AB-SNAREpin complexes on the surface of negatively charged lipid nanotube flipped along z-axis. 10.4A resolution. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.49 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
CCP4 map header:
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-Supplemental data
-Mask #1
File | emd_9231_msk_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Half map: Half-map 1 used for FSC calculation
File | emd_9231_half_map_1.map | ||||||||||||
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Annotation | Half-map 1 used for FSC calculation | ||||||||||||
Projections & Slices |
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Density Histograms |
-Half map: Half-map 2 used for FSC calculation
File | emd_9231_half_map_2.map | ||||||||||||
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Annotation | Half-map 2 used for FSC calculation | ||||||||||||
Projections & Slices |
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Density Histograms |
-Sample components
-Entire : Synaptotagmin 1 C2AB in a complex with the SNAREpin assembly boun...
Entire | Name: Synaptotagmin 1 C2AB in a complex with the SNAREpin assembly bound to the negatively charged phospholipid nanotube in presence of Mg2+. |
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Components |
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-Supramolecule #1: Synaptotagmin 1 C2AB in a complex with the SNAREpin assembly boun...
Supramolecule | Name: Synaptotagmin 1 C2AB in a complex with the SNAREpin assembly bound to the negatively charged phospholipid nanotube in presence of Mg2+. type: complex / ID: 1 / Parent: 0 / Macromolecule list: all |
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Source (natural) | Organism: Rattus norvegicus (Norway rat) |
Recombinant expression | Organism: Escherichia coli 'BL21-Gold(DE3)pLysS AG' (bacteria) |
-Macromolecule #1: Synaptotagmin 1
Macromolecule | Name: Synaptotagmin 1 / type: protein_or_peptide / ID: 1 / Enantiomer: LEVO |
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Sequence | String: KLGKLQYSLD YDFQNNQLLV GIIQAAELPA LDMGGTSDPY VKVFLLPDKK KKFETKVHRK TLNPVFNEQF TFKVPYSELG GKTLVMAVYD FDRFSKHDII GEFKVPMNTV DFGHVTEEWR DLQSAEKEEQ EKLGDICFSL RYVPTAGKLT VVILEAKNLK KMDVGGLSDP ...String: KLGKLQYSLD YDFQNNQLLV GIIQAAELPA LDMGGTSDPY VKVFLLPDKK KKFETKVHRK TLNPVFNEQF TFKVPYSELG GKTLVMAVYD FDRFSKHDII GEFKVPMNTV DFGHVTEEWR DLQSAEKEEQ EKLGDICFSL RYVPTAGKLT VVILEAKNLK KMDVGGLSDP YVKIHLMQNG KRLKKKKTTI KKNTLNPYYN ESFSFEVPFE QIQKVQVVVT VLDYDKIGKN DAIGKVFVGY NSTGAELRHW SDMLANPRRP IAQWHTLQVE EEVDAMLAVK K |
-Macromolecule #2: Vesicle-associated membrane protein 2
Macromolecule | Name: Vesicle-associated membrane protein 2 / type: protein_or_peptide / ID: 2 / Enantiomer: LEVO |
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Sequence | String: GSNRRLQQTQ AQVDEVVDIM RVNVDKVLER DQKLSELDDR ADALQAGASQ FETSAAKLKR KYW |
-Macromolecule #3: Syntaxin-1A
Macromolecule | Name: Syntaxin-1A / type: protein_or_peptide / ID: 3 / Enantiomer: LEVO |
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Sequence | String: MALSEIETRH SEIIKLENSI RELHDMFMDM AMLVESQGEM IDRIEYNVEH AVDYVERAVS DTKKAVK |
-Macromolecule #4: Synaptosomal-associated protein 25
Macromolecule | Name: Synaptosomal-associated protein 25 / type: protein_or_peptide / ID: 4 / Enantiomer: LEVO |
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Sequence | String: MRNELEEMQR RADQLADESL ESTRRMLQLV EESKDAGIRT LVMLDEQGEQ LDRVEEGMNH INQDMKEAEK NLKDLGK |
-Macromolecule #5: Synaptosomal-associated protein 25
Macromolecule | Name: Synaptosomal-associated protein 25 / type: protein_or_peptide / ID: 5 / Enantiomer: LEVO |
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Sequence | String: MARENEMDEN LEQVSGIIGN LRHMALDMGN EIDTQNRQID RIMEKADSNK TRIDEANQRA TKMLG |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | helical reconstruction |
Aggregation state | helical array |
-Sample preparation
Buffer | pH: 7.4 |
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Vitrification | Cryogen name: ETHANE / Instrument: FEI VITROBOT MARK III |
-Electron microscopy
Microscope | FEI TECNAI F20 |
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Image recording | Film or detector model: GATAN K2 SUMMIT (4k x 4k) / Detector mode: COUNTING / Average exposure time: 9.9 sec. / Average electron dose: 44.0 e/Å2 |
Electron beam | Acceleration voltage: 200 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD |
Experimental equipment | Model: Tecnai F20 / Image courtesy: FEI Company |
-Image processing
-Atomic model buiding 1
Refinement | Protocol: RIGID BODY FIT |
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Output model | PDB-6mti: |