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Allosteric regulation of pentameric ligand-gated ion channels: An emerging mechanistic perspective

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  • معلومة اضافية
    • Contributors:
      Laboratoire de biochimie théorique Paris (LBT (UPR_9080)); Institut de biologie physico-chimique (IBPC (FR_550)); Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Diderot - Paris 7 (UPD7)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS); Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS); Génétique Humaine et Fonctions Cognitives; Institut Pasteur Paris (IP)-Centre National de la Recherche Scientifique (CNRS); University of California San Diego (UC San Diego); University of California (UC); Collège de France (CdF (institution)); Institut de Science et d'ingénierie supramoléculaires (ISIS); Université de Strasbourg (UNISTRA)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)-Matériaux et Nanosciences Grand-Est (MNGE); Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Réseau nanophotonique et optique; Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)
    • بيانات النشر:
      HAL CCSD
      Taylor & Francis
    • الموضوع:
      2014
    • Collection:
      Institut Pasteur: HAL
    • نبذة مختصرة :
      International audience ; Pentameric ligand-gated ion channels (pLGICs) play a central role in intercellular communications in the nervous system by converting the binding of a chemical messenger—a neurotransmitter—into an ion flux through the postsynaptic membrane. They are oligomeric assemblies that provide prototypical examples of allosterically regulated integral membrane proteins. Here, we present an overview of the most recent advances on the signal transduction mechanism based on the X-ray structures of both prokaryotic and invertebrate eukaryotic pLGICs and atomistic Molecular Dynamics simulations. The present results suggest that ion gating involves a large structural reorganization of the molecule mediated by two distinct quaternary transitions, a global twisting and the blooming of the extracellular domain, which can be modulated by ligand binding at the topographically distinct orthosteric and allosteric sites. The emerging model of gating is consistent with a wealth of functional studies and will boost the development of novel pharmacological strategies.
    • Relation:
      info:eu-repo/semantics/altIdentifier/pmid/25478624; hal-01498037; https://hal.science/hal-01498037; https://hal.science/hal-01498037/document; https://hal.science/hal-01498037/file/chan-8-350.pdf; PUBMED: 25478624; PUBMEDCENTRAL: PMC4203737
    • الرقم المعرف:
      10.4161/chan.29444
    • Rights:
      info:eu-repo/semantics/OpenAccess
    • الرقم المعرف:
      edsbas.4F819280