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Yorodumi- EMDB-71303: Cryo-EM structure of full-length human TRPV1 in the presence of a... -
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Basic information
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| Title | Cryo-EM structure of full-length human TRPV1 in the presence of alpha-humulene | |||||||||||||||
Map data | Cryo-EM structure of full-length human TRPV1 in the presence of alpha-humulene | |||||||||||||||
Sample |
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Keywords | transient receptor potential V family member 1 / TRP / channel / TRPV1 / TRP channels / sesquiterpene / alpha-humulene / pain / analgesia / MEMBRANE PROTEIN | |||||||||||||||
| Function / homology | Function and homology informationchemosensory behavior / response to capsazepine / sensory perception of mechanical stimulus / peptide secretion / excitatory extracellular ligand-gated monoatomic ion channel activity / temperature-gated ion channel activity / detection of chemical stimulus involved in sensory perception of pain / smooth muscle contraction involved in micturition / fever generation / detection of temperature stimulus involved in thermoception ...chemosensory behavior / response to capsazepine / sensory perception of mechanical stimulus / peptide secretion / excitatory extracellular ligand-gated monoatomic ion channel activity / temperature-gated ion channel activity / detection of chemical stimulus involved in sensory perception of pain / smooth muscle contraction involved in micturition / fever generation / detection of temperature stimulus involved in thermoception / thermoception / cellular response to acidic pH / dendritic spine membrane / TRP channels / diet induced thermogenesis / cellular response to alkaloid / cellular response to ATP / detection of temperature stimulus involved in sensory perception of pain / intracellularly gated calcium channel activity / behavioral response to pain / calcium ion import across plasma membrane / voltage-gated calcium channel activity / extracellular ligand-gated monoatomic ion channel activity / phosphatidylinositol binding / phosphoprotein binding / GABA-ergic synapse / calcium ion transmembrane transport / calcium channel activity / lipid metabolic process / transmembrane signaling receptor activity / sensory perception of taste / cellular response to heat / protein homotetramerization / postsynaptic membrane / calmodulin binding / cell surface receptor signaling pathway / negative regulation of transcription by RNA polymerase II / ATP binding / metal ion binding / membrane / plasma membrane Similarity search - Function | |||||||||||||||
| Biological species | Homo sapiens (human) | |||||||||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 2.74 Å | |||||||||||||||
Authors | Talyzina IA / Sobolevsky AI | |||||||||||||||
| Funding support | United States, 4 items
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Citation | Journal: Proc Natl Acad Sci U S A / Year: 2025Title: Structural basis of the inhibition of TRPV1 by analgesic sesquiterpenes. Authors: Raúl Sánchez-Hernández / Miguel Benítez-Angeles / Irina A Talyzina / Itzel Llorente / Mariela González-Avendaño / Félix Sierra / Angélica Méndez-Reséndiz / Francisco Mercado / ...Authors: Raúl Sánchez-Hernández / Miguel Benítez-Angeles / Irina A Talyzina / Itzel Llorente / Mariela González-Avendaño / Félix Sierra / Angélica Méndez-Reséndiz / Francisco Mercado / Ariela Vergara-Jaque / Alexander I Sobolevsky / León D Islas / Tamara Rosenbaum / ![]() Abstract: The Transient Receptor Potential Vanilloid 1 (TRPV1) ion channel is expressed in primary nociceptive afferents, which participate in processes such as pain and inflammation. Considerable efforts have ...The Transient Receptor Potential Vanilloid 1 (TRPV1) ion channel is expressed in primary nociceptive afferents, which participate in processes such as pain and inflammation. Considerable efforts have been directed toward finding inhibitors of TRPV1 and understanding the molecular details of their interactions with this channel. α-humulene (AH) is a sesquiterpene derived from plants such as hops and other members of Cannabaceae family, with a long history of popular use as an analgesic and anti-inflammatory. Using a combination of behavioral assays, electrophysiology, site-directed mutagenesis, cryo-EM, and molecular dynamics simulations, we show that AH inhibits TRPV1-related pain responses and currents by interacting with a region composed of the S2, S2-S3 linker, and S3 transmembrane segments and stabilizing the closed conformation of the channel. The interaction of ligands in this region of the TRPV1 channel has not been previously described and the results of the present study highlight that it may constitute part of a negative regulatory region. These findings allow us to understand the molecular basis by which substances such as some sesquiterpenes, abundantly found in medicinal plants used by humans for hundreds of years, reduce pain. Pain management can include the use of opioids, which results in hepatic and renal damage and possible addiction. Our study offers insight into a poorly understood group of compounds that could be used as scaffold to produce novel nonopioid analgesic therapies and clarifies the molecular mechanisms that underlie the effects of these analgesic molecules. | |||||||||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_71303.map.gz | 117.9 MB | EMDB map data format | |
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| Header (meta data) | emd-71303-v30.xml emd-71303.xml | 23.2 KB 23.2 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_71303_fsc.xml | 12 KB | Display | FSC data file |
| Images | emd_71303.png | 61.2 KB | ||
| Filedesc metadata | emd-71303.cif.gz | 7.5 KB | ||
| Others | emd_71303_half_map_1.map.gz emd_71303_half_map_2.map.gz | 115.8 MB 115.8 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-71303 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-71303 | HTTPS FTP |
-Validation report
| Summary document | emd_71303_validation.pdf.gz | 964.6 KB | Display | EMDB validaton report |
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| Full document | emd_71303_full_validation.pdf.gz | 964.2 KB | Display | |
| Data in XML | emd_71303_validation.xml.gz | 19 KB | Display | |
| Data in CIF | emd_71303_validation.cif.gz | 24.6 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-71303 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-71303 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 9p6bMC M: atomic model generated by this map C: citing same article ( |
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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_71303.map.gz / Format: CCP4 / Size: 125 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Annotation | Cryo-EM structure of full-length human TRPV1 in the presence of alpha-humulene | ||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 0.635 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Half map: Half Map A
| File | emd_71303_half_map_1.map | ||||||||||||
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| Annotation | Half Map A | ||||||||||||
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-Half map: Half Map B
| File | emd_71303_half_map_2.map | ||||||||||||
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| Annotation | Half Map B | ||||||||||||
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| Density Histograms |
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Sample components
-Entire : full-length human TRPV1 in the presence of alpha-humulene
| Entire | Name: full-length human TRPV1 in the presence of alpha-humulene |
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| Components |
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-Supramolecule #1: full-length human TRPV1 in the presence of alpha-humulene
| Supramolecule | Name: full-length human TRPV1 in the presence of alpha-humulene type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1 |
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| Source (natural) | Organism: Homo sapiens (human) |
| Molecular weight | Theoretical: 500 KDa |
-Macromolecule #1: Transient receptor potential cation channel subfamily V member 1
| Macromolecule | Name: Transient receptor potential cation channel subfamily V member 1 type: protein_or_peptide / ID: 1 / Number of copies: 4 / Enantiomer: LEVO |
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| Source (natural) | Organism: Homo sapiens (human) |
| Molecular weight | Theoretical: 124.575281 KDa |
| Recombinant expression | Organism: Homo sapiens (human) |
| Sequence | String: MTSKKWSSTD LGAAADPLQK DTCPDPLDGD PNSRPPPAKP QLSTAKSRTR LFGKGDSEEA FPVDCPHEEG ELDSCPTITV SPVITIQRP GDGPTGARLL SQDSVAASTE KTLRLYDRRS IFEAVAQNNC QDLESLLLFL QKSKKHLTDN EFKDPETGKT C LLKAMLNL ...String: MTSKKWSSTD LGAAADPLQK DTCPDPLDGD PNSRPPPAKP QLSTAKSRTR LFGKGDSEEA FPVDCPHEEG ELDSCPTITV SPVITIQRP GDGPTGARLL SQDSVAASTE KTLRLYDRRS IFEAVAQNNC QDLESLLLFL QKSKKHLTDN EFKDPETGKT C LLKAMLNL HDGQNTTIPL LLEIARQTDS LKELVNASYT DSYYKGQTAL HIAIERRNMA LVTLLVENGA DVQAAAHGDF FK KTKGRPG FYFGELPLSL AACTNQLGIV KFLLQNSWQT ADISARDSVG NTVLHALVEV ADNTADNTKF VTSMYNEILM LGA KLHPTL KLEELTNKKG MTPLALAAGT GKIGVLAYIL QREIQEPECR HLSRKFTEWA YGPVHSSLYD LSCIDTCEKN SVLE VIAYS SSETPNRHDM LLVEPLNRLL QDKWDRFVKR IFYFNFLVYC LYMIIFTMAA YYRPVDGLPP FKMEKTGDYF RVTGE ILSV LGGVYFFFRG IQYFLQRRPS MKTLFVDSYS EMLFFLQSLF MLATVVLYFS HLKEYVASMV FSLALGWTNM LYYTRG FQQ MGIYAVMIEK MILRDLCRFM FVYIVFLFGF STAVVTLIED GKNDSLPSES TSHRWRGPAC RPPDSSYNSL YSTCLEL FK FTIGMGDLEF TENYDFKAVF IILLLAYVIL TYILLLNMLI ALMGETVNKI AQESKNIWKL QRAITILDTE KSFLKCMR K AFRSGKLLQV GYTPDGKDDY RWCFRVDEVN WTTWNTNVGI INEDPGNCEG VKRTLSFSLR SSRVSGRHWK NFALVPLLR EASARDRQSA QPEEVYLRQF SGSLKPEDAE VFKSPAASGE KLVPRGSAAA AVSKGEELFT GVVPILVELD GDVNGHKFSV SGEGEGDAT YGKLTLKFIC TTGKLPVPWP TLVTTLTYGV QCFSRYPDHM KQHDFFKSAM PEGYVQERTI FFKDDGNYKT R AEVKFEGD TLVNRIELKG IDFKEDGNIL GHKLEYNYNS HNVYIMADKQ KNGIKVNFKI RHNIEDGSVQ LADHYQQNTP IG DGPVLLP DNHYLSTQSK LSKDPNEKRD HMVLLEFVTA AGITLGMDEL YKSGLRSWSH PQFEK UniProtKB: Transient receptor potential cation channel subfamily V member 1 |
-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: 32 / Formula: POV |
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| Molecular weight | Theoretical: 760.076 Da |
| Chemical component information | ![]() ChemComp-POV: |
-Macromolecule #3: (2R)-3-{[(R)-hydroxy{[(1S,2R,3R,4S,5S,6R)-2,3,4,5,6-pentahydroxyc...
| Macromolecule | Name: (2R)-3-{[(R)-hydroxy{[(1S,2R,3R,4S,5S,6R)-2,3,4,5,6-pentahydroxycyclohexyl]oxy}phosphoryl]oxy}propane-1,2-diyl dioctadecanoate type: ligand / ID: 3 / Number of copies: 4 / Formula: 8IJ |
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| Molecular weight | Theoretical: 867.138 Da |
| Chemical component information | ![]() ChemComp-8IJ: |
-Macromolecule #4: TRIDECANE
| Macromolecule | Name: TRIDECANE / type: ligand / ID: 4 / Number of copies: 4 / Formula: TRD |
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| Molecular weight | Theoretical: 184.361 Da |
| Chemical component information | ![]() ChemComp-TRD: |
-Macromolecule #5: SODIUM ION
| Macromolecule | Name: SODIUM ION / type: ligand / ID: 5 / Number of copies: 2 |
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| Molecular weight | Theoretical: 22.99 Da |
-Macromolecule #6: water
| Macromolecule | Name: water / type: ligand / ID: 6 / Number of copies: 92 / Formula: HOH |
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| Molecular weight | Theoretical: 18.015 Da |
| Chemical component information | ![]() ChemComp-HOH: |
-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 | 2.4 mg/mL | ||||||||||||
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| Buffer | pH: 7 Component:
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| Grid | Model: UltrAuFoil R1.2/1.3 / Material: GOLD / Mesh: 300 / Support film - Material: GOLD / Support film - topology: HOLEY | ||||||||||||
| Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 295 K / Instrument: FEI VITROBOT MARK IV | ||||||||||||
| Details | human TRPV1 |
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Electron microscopy
| Microscope | TFS KRIOS |
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| Image recording | Film or detector model: GATAN K3 (6k x 4k) / Digitization - Dimensions - Width: 5760 pixel / Digitization - Dimensions - Height: 4092 pixel / Number grids imaged: 1 / Number real images: 9208 / Average exposure time: 1.318 sec. / 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 / Cs: 2.7 mm / Nominal defocus max: 2.2 µm / Nominal defocus min: 0.7000000000000001 µm |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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Image processing
-Atomic model buiding 1
| Refinement | Space: REAL |
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| Output model | ![]() PDB-9p6b: |
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About Yorodumi



Keywords
Homo sapiens (human)
Authors
United States, 4 items
Citation




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FIELD EMISSION GUN

