From the Department of Anesthesia Critical Care and Pain Medicine, Massachusetts General Hospital, Boston, Massachusetts 02114,; the Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115, and.
From the Department of Anesthesia Critical Care and Pain Medicine, Massachusetts General Hospital, Boston, Massachusetts 02114.
J Biol Chem. 2013 Oct 18;288(42):30373-30386. doi: 10.1074/jbc.M113.494583. Epub 2013 Sep 5.
Etomidate is a potent general anesthetic that acts as an allosteric co-agonist at GABAA receptors. Photoreactive etomidate derivatives labeled αMet-236 in transmembrane domain M1, which structural models locate in the β+/α- subunit interface. Other nearby residues may also contribute to etomidate binding and/or transduction through rearrangement of the site. In human α1β2γ2L GABAA receptors, we applied the substituted cysteine accessibility method to α1-M1 domain residues extending from α1Gln-229 to α1Gln-242. We used electrophysiology to characterize each mutant's sensitivity to GABA and etomidate. We also measured rates of sulfhydryl modification by p-chloromercuribenzenesulfonate (pCMBS) with and without GABA and tested if etomidate blocks modification of pCMBS-accessible cysteines. Cys substitutions in the outer α1-M1 domain impaired GABA activation and variably affected etomidate sensitivity. In seven of eight residues where pCMBS modification was evident, rates of modification were accelerated by GABA co-application, indicating that channel activation increases water and/or pCMBS access. Etomidate reduced the rate of modification for cysteine substitutions at α1Met-236, α1Leu-232 and α1Thr-237. We infer that these residues, predicted to face β2-M3 or M2 domains, contribute to etomidate binding. Thus, etomidate interacts with a short segment of the outer α1-M1 helix within a subdomain that undergoes significant structural rearrangement during channel gating. Our results are consistent with in silico docking calculations in a homology model that orient the long axis of etomidate approximately orthogonal to the transmembrane axis.
依托咪酯是一种强效的全身麻醉药,作为 GABA A 受体的变构共激动剂。光反应依托咪酯衍生物标记在跨膜域 M1 中的αMet-236,结构模型定位在β+/α-亚基界面。其他附近的残基也可能通过该位点的重排有助于依托咪酯的结合和/或转导。在人类α1β2γ2L GABA A 受体中,我们应用取代的半胱氨酸可及性方法来研究从α1Gln-229延伸到α1Gln-242的α1-M1 结构域残基。我们使用电生理学来表征每个突变体对 GABA 和依托咪酯的敏感性。我们还测量了 p-氯汞苯磺酸盐(pCMBS)与 GABA 一起和不一起时对巯基修饰的速率,并测试了依托咪酯是否阻断 pCMBS 可及半胱氨酸的修饰。外α1-M1 结构域中的 Cys 取代会损害 GABA 的激活,并不同程度地影响依托咪酯的敏感性。在 pCMBS 修饰明显的八个残基中的七个中,修饰速率通过 GABA 共同应用而加速,表明通道激活增加了水和/或 pCMBS 的可及性。依托咪酯降低了α1Met-236、α1Leu-232 和α1Thr-237 处半胱氨酸取代的修饰速率。我们推断,这些残基,预测与β2-M3 或 M2 结构域相对,有助于依托咪酯的结合。因此,依托咪酯与通道门控过程中发生显著结构重排的外α1-M1 螺旋的短片段相互作用。我们的结果与同源模型中的计算机对接计算结果一致,该模型使依托咪酯的长轴大致垂直于跨膜轴。