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Copper and protons directly activate the zinc-activated channel.
Trattnig, Sarah M; Gasiorek, Agnes; Deeb, Tarek Z; Ortiz, Eydith J Comenencia; Moss, Stephen J; Jensen, Anders A; Davies, Paul A.
Afiliación
  • Trattnig SM; Department of Neuroscience, Tufts University School of Medicine, Boston, MA 02111, USA; Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Universitetsparken 2, DK-2100 Copenhagen, Denmark. Electronic address: sarahmaria.trattnig@gmail.com.
  • Gasiorek A; Department of Neuroscience, Tufts University School of Medicine, Boston, MA 02111, USA; Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Universitetsparken 2, DK-2100 Copenhagen, Denmark. Electronic address: agnes.gasiorek@sund.ku.dk.
  • Deeb TZ; Department of Neuroscience, Tufts University School of Medicine, Boston, MA 02111, USA. Electronic address: Tarek.Deeb@tufts.edu.
  • Ortiz EJ; Department of Neuroscience, Tufts University School of Medicine, Boston, MA 02111, USA. Electronic address: eydith@gmail.com.
  • Moss SJ; Department of Neuroscience, Tufts University School of Medicine, Boston, MA 02111, USA. Electronic address: Stephen.Moss@tufts.edu.
  • Jensen AA; Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Universitetsparken 2, DK-2100 Copenhagen, Denmark. Electronic address: aaj@sund.ku.dk.
  • Davies PA; Department of Neuroscience, Tufts University School of Medicine, Boston, MA 02111, USA. Electronic address: paul.davies@tufts.edu.
Biochem Pharmacol ; 103: 109-17, 2016 Mar 01.
Article en En | MEDLINE | ID: mdl-26872532
ABSTRACT
The zinc-activated channel (ZAC) is a cationic ion channel belonging to the superfamily of Cys-loop receptors, which consists of pentameric ligand-gated ion channels. ZAC is the least understood member of this family so in the present study we sought to characterize the properties of this channel further. We demonstrate that not only zinc (Zn(2+)) but also copper (Cu(2+)) and protons (H(+)) are agonists of ZAC, displaying potencies and efficacies in the rank orders of H(+)>Cu(2+)>Zn(2+) and H(+)>Zn(2+)>Cu(2+), respectively. The responses elicited by Zn(2+), Cu(2+) and H(+) through ZAC are all characterized by low degrees of desensitization. In contrast, currents evoked by high concentrations of the three agonists comprise distinctly different activation and decay components, with transitions to and from an open state being significantly faster for H(+) than for the two metal ions. The permeabilities of ZAC for Na(+) and K(+) relative to Cs(+) are indistinguishable, whereas replacing all of extracellular Na(+) and K(+) with the divalent cations Ca(2+) or Mg(2+) results in complete elimination of Zn(2+)-activated currents at both negative and positive holding potentials. This indicates that ZAC is non-selectively permeable to monovalent cations, whereas Ca(2+) and Mg(2+) inhibit the channel. In conclusion, this is the first report of a Cys-loop receptor being gated by Zn(2+), Cu(2+) and H(+). ZAC could be an important mediator of some of the wide range of physiological functions regulated by or involving Zn(2+), Cu(2+) and H(+).
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Protones / Zinc / Cobre / Canales Iónicos Límite: Animals / Humans Idioma: En Revista: Biochem Pharmacol Año: 2016 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Protones / Zinc / Cobre / Canales Iónicos Límite: Animals / Humans Idioma: En Revista: Biochem Pharmacol Año: 2016 Tipo del documento: Article
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