Title: The Novel Anticonvulsant Drug, Gabapentin (Neurontin), Binds to the α2δ Subunit of a Calcium Channel
Abstract: Gabapentin (1-(aminomethyl)cyclohexane acetic acid; Neurontin) is a novel anticonvulsant drug, with a mechanism of action apparently dissimilar to that of other antiepileptic agents. We report here the isolation and characterization of a [<sup>3</sup>H]gabapentin-binding protein from pig cerebral cortex membranes. The detergent-solubilized binding protein was purified 1022-fold, in a six-step column-chromatographic procedure, with a yield of 3.9%. The purified protein had an apparent subunit <i>M</i><sub>r</sub> of 130,000, and was heavily glycosylated. The partial N-terminal amino acid sequence of the <i>M</i><sub>r</sub> 130,000 polypeptide, EPFPSAVTIK, was identical to that reported for the α<sub>2</sub>δ subunit of the L-type Ca<sup>2+</sup> channel from rabbit skeletal muscle (Hamilton, S. L., Hawkes, M. J., Brush, K., Cook, R., Chang, R. J., and Smilowitz, H. M.(1989) <i>Biochemistry</i> 28, 7820-7828). High levels of [<sup>3</sup>H]gabapentin binding sites were found in membranes prepared from rat brain, heart and skeletal muscle. Binding of [<sup>3</sup>H]gabapentin to COS-7 cells transfected with α<sub>2</sub>δ cDNA was elevated >10-fold over controls, consistent with the expression of α<sub>2</sub>δ protein, as measured by Western blotting. Finally, purified L-type Ca<sup>2+</sup> channel complexes were fractionated, under dissociating conditions, on an ion-exchange column; [<sup>3</sup>H]gabapentin binding activity closely followed the elution of the α<sub>2</sub>δ subunit. [<sup>3</sup>H]Gabapentin is the first pharmacological agent described that interacts with an α<sub>2</sub>δ subunit of a voltage-dependent Ca<sup>2+</sup> channel.