Abstract

The α7-type nicotinic acetylcholine receptor (nAChR) has been recognized as a potential therapeutic target for the treatment of a variety of pathologic conditions, including schizophrenia, Alzheimer's disease, and peripheral inflammation. A unique feature of α7 nAChRs that tends to complicate functional assays intended to identify selective drugs for these receptors is the strong concentration-dependent desensitization of their agonist-evoked responses. At low agonist concentrations, voltage-clamp responses are small but tend to closely follow the solution exchange profile, whereas higher agonist concentrations produce responses that peak and then decay very rapidly, usually before the full drug concentration has been achieved. In this article, we report that an α7 T245S mutant, which has a point mutation at the sixth position in the α7 second transmembrane domain (T6′S), demonstrates a significant gain of function, sustaining current when exposed to relatively high agonist concentrations when expressed in Xenopus laevis oocytes and larger peak currents when expressed in mammalian GH4C1 cells. At the single-channel level, the T6′S mutant has a unitary conductance of 61.7 ± 5.8 pS, similar to that reported for wild-type α7, but a vastly longer average open duration. In addition, channel burst activity indicates a greater than 40% probability of channel re-opening in the sustained presence of 30 μM acetylcholine, consistent with a greater overall open probability relative to wild-type α7. Unlike the α7 L248T gain-of-function mutant, the T6′S mutant exhibits a pharmacological profile that is remarkably similar to the wild-type α7 receptor, implicating it as a potentially useful tool for identifying therapeutic agents.