Identification of residues critical for Cu2+-mediated inhibition of glycine alpha1 receptors.

Article Details

Citation

Copy to clipboard

Chen Z, Dillon GH, Huang R

Identification of residues critical for Cu2+-mediated inhibition of glycine alpha1 receptors.

Neuropharmacology. 2006 Sep;51(4):701-8. Epub 2006 Jul 12.

PubMed ID

16842826 [ View in PubMed

]

Abstract

Endogenous divalent cations Cu2+ and Zn2+ suppress the activity of glycine receptors (glyRs). Whereas residues critical for the effects of Zn2+ on glyRs have been identified, little is known about the determinants of Cu2+-mediated inhibition. In the present studies, we have assessed the potential commonality of Zn2+ and Cu2+-mediated inhibition of glyRs. Cu2+ potently inhibited recombinant human glycine alpha1 receptors, with an IC50 of 4.1+/-0.7 microM. Systematic mutation of extracellular histidine residues revealed that mutation H215A greatly reduced the inhibitory modulation by Cu2+. Substitution of H215 with C produced receptors with Cu2+ sensitivity similar to the wild type. Furthermore, modification of H215C with a thio-specific reagent, [2-(trimethylammonium)ethyl] methanethiosulfonate bromide (MTSET), reduced Cu2+ sensitivity of H215C receptors. However, mutation of other extracellular histidine residues including H107 and H109, which are known inhibitory Zn2+coordination sites, failed to influence inhibition of glycine currents by Cu2+. Moreover, mutation to alanine of two threonine residues (T112, T133) critical for Zn2+ inhibition had no effect (T133A) or only partial inhibitory effects (T112A) on Cu2+-induced inhibition. The double mutation, T112A/H215A, caused greater effects on Cu2+-mediated inhibition than either mutation alone. In addition, the glycine currents recorded from T112A/H215A mutant receptors were significantly potentiated by low concentrations of Cu2+. Our results have identified critical determinants of Cu2+-mediated inhibition of glyRs. Moreover, we demonstrate for the first time a clear difference in residues responsible for Cu2+-mediated compared to Zn2+-mediated inhibition of glyRs.

DrugBank Data that Cites this Article

Drug Targets

Drug	Target	Kind	Organism	Pharmacological Action	Actions
Copper	Glycine receptor subunit alpha-1	Protein	Humans	Unknown	Not Available	Details
Zinc	Glycine receptor subunit alpha-1	Protein	Humans	Unknown	Not Available	Details
Zinc acetate	Glycine receptor subunit alpha-1	Protein	Humans	Unknown	Not Available	Details
Zinc chloride	Glycine receptor subunit alpha-1	Protein	Humans	Unknown	Inhibitor	Details
Zinc sulfate, unspecified form	Glycine receptor subunit alpha-1	Protein	Humans	Unknown	Inhibitor	Details