PT - JOURNAL ARTICLE AU - J. Glen Newell AU - Ross A. McDevitt AU - Cynthia Czajkowski TI - Mutation of Glutamate 155 of the GABA<sub>A</sub> Receptor β<sub>2</sub> Subunit Produces a Spontaneously Open Channel: A Trigger for Channel Activation AID - 10.1523/JNEUROSCI.3746-04.2004 DP - 2004 Dec 15 TA - The Journal of Neuroscience PG - 11226--11235 VI - 24 IP - 50 4099 - http://www.jneurosci.org/content/24/50/11226.short 4100 - http://www.jneurosci.org/content/24/50/11226.full SO - J. Neurosci.2004 Dec 15; 24 AB - Protein movements underlying ligand-gated ion channel activation are poorly understood. The binding of agonist initiates a series of conformational movements that ultimately lead to the opening of the ion channel pore. Although little is known about local movements within the GABA-binding site, a recent structural model of the GABAA receptor (GABAAR) ligand-binding domain predicts that β2Glu155 is a key residue for direct interactions with the neurotransmitter (Cromer et al., 2002). To elucidate the role of the β2Ile154-Asp163 region in GABAAR activation, each residue was individually mutated to cysteine and coexpressed with wild-type α1 subunits in Xenopus laevis oocytes. Seven mutations increased the GABA EC50 value (8- to 3400-fold), whereas three mutations (E155C, S156C, and G158C) also significantly increased the 2-(3-carboxypropyl)-3-amino-6-(4-methoxyphenyl) pyridazinium (SR-95531) KI value. GABA, SR-95531, and pentobarbital slowed N-biotinylaminoethyl methanethiosulfonate modification of T160C and D163C, indicating that β2Thr160 and β2Asp163 are located in or near the GABA-binding site and that this region undergoes structural rearrangements during channel gating. Cysteine substitution of β2Glu155 resulted in spontaneously open GABAARs and differentially decreased the GABA, piperidine-4-sulfonic acid (partial agonist), and SR-95531 sensitivities, indicating that the mutation perturbs ligand binding as well as channel gating. Tethering thiol-reactive groups onto β2E155C closed the spontaneously open channels, suggesting that β2Glu155 is a control element involved in coupling ligand binding to channel gating. Structural modeling suggests that the β2 Ile154-Asp163 region is a protein hinge that forms a network of interconnections that couples binding site movements to the cascade of events leading to channel opening.