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Cannabinoid non-cannabidiol site modulation of TRPV2 structure and function

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    SYSNO ASEP0565702
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleCannabinoid non-cannabidiol site modulation of TRPV2 structure and function
    Author(s) Zhang, L. (SE)
    Simonsen, Ch. (SE)
    Zímová, Lucie (FGU-C) RID, ORCID
    Wang, K. (DK)
    Moparthi, L. (SE)
    Gaudet, R. (US)
    Ekoff, M. (SE)
    Nilsson, G. (SE)
    Hellmich, U. A. (DE)
    Vlachová, Viktorie (FGU-C) RID, ORCID, SAI
    Gourdon, P. (SE)
    Zygmunt, P. M. (SE)
    Article number7483
    Source TitleNature Communications. - : Nature Publishing Group
    Roč. 13, č. 1 (2022)
    Number of pages18 s.
    Languageeng - English
    CountryGB - United Kingdom
    KeywordsTRPV cation channels ; cannabinoids ; cannabidiol ; ligand ; TRPV2 protein
    OECD categoryNeurosciences (including psychophysiology
    R&D ProjectsGA22-13750S GA ČR - Czech Science Foundation (CSF)
    Method of publishingOpen access
    Institutional supportFGU-C - RVO:67985823
    UT WOS000952021200020
    EID SCOPUS85143312444
    DOI10.1038/s41467-022-35163-y
    AnnotationTRPV2 is a ligand-operated temperature sensor with poorly defined pharmacology. Here, we combine calcium imaging and patch-clamp electrophysiology with cryo-electron microscopy (cryo-EM) to explore how TRPV2 activity is modulated by the phytocannabinoid delta9-tetrahydrocannabiorcol (C16) and by probenecid. C16 and probenecid act in concert to stimulate TRPV2 responses including histamine release from rat and human mast cells. Each ligand causes distinct conformational changes in TRPV2 as revealed by cryo-EM. Although the binding for probenecid remains elusive, C16 associates within the vanilloid pocket. As such, the C16 binding location is distinct from that of cannabidiol, partially overlapping with the binding site of the TRPV2 inhibitor piperlongumine. Taken together, we discover a new cannabinoid binding site in TRPV2 that is under the influence of allosteric control by probenecid. This molecular insight into ligand modulation enhances our understanding of TRPV2 in normal and pathophysiology.
    WorkplaceInstitute of Physiology
    ContactLucie Trajhanová, lucie.trajhanova@fgu.cas.cz, Tel.: 241 062 400
    Year of Publishing2023
    Electronic addresshttps://doi.org/10.1038/s41467-022-35163-y
Number of the records: 1  

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