Department of Pharmacology, University of Washington, Seattle, WA 98195-7280, USA.
Proc Natl Acad Sci U S A. 2011 Nov 15;108(46):18825-30. doi: 10.1073/pnas.1116449108. Epub 2011 Oct 31.
Voltage-gated Na(+) channels initiate action potentials during electrical signaling in excitable cells. Opening and closing of the pore of voltage-gated ion channels are mechanically linked to voltage-driven outward movement of the positively charged S4 transmembrane segment in their voltage sensors. Disulfide locking of cysteine residues substituted for the outermost T0 and R1 gating-charge positions and a conserved negative charge (E43) at the extracellular end of the S1 segment of the bacterial Na(+) channel NaChBac detects molecular interactions that stabilize the resting state of the voltage sensor and define its conformation. Upon depolarization, the more inward gating charges R2 and R3 engage in these molecular interactions as the S4 segment moves outward to its intermediate and activated states. The R4 gating charge does not disulfide-lock with E43, suggesting an outer limit to its transmembrane movement. These molecular interactions reveal how the S4 gating charges are stabilized in the resting state and how their outward movement is catalyzed by interaction with negatively charged residues to effect pore opening and initiate electrical signaling.
电压门控钠离子通道在可兴奋细胞的电信号传递过程中引发动作电位。电压门控离子通道的孔的开启和关闭与电压驱动的其电压传感器中带正电荷的 S4 跨膜片段向外移动机械相连。用二硫键锁定取代最外层 T0 和 R1 门控电荷位置的半胱氨酸残基以及 S1 片段胞外端的保守负电荷 (E43),细菌钠离子通道 NaChBac 检测到稳定电压传感器静息状态并定义其构象的分子相互作用。去极化时,当 S4 片段向外移动到其中间和激活状态时,更向内的门控电荷 R2 和 R3 参与这些分子相互作用。R4 门控电荷不会与 E43 形成二硫键,表明其跨膜运动的外部限制。这些分子相互作用揭示了 S4 门控电荷如何在静息状态下稳定,以及它们如何通过与带负电荷的残基相互作用向外移动来促进孔的打开并引发电信号传递。