Yang N, George A L, Horn R
Department of Physiology, Jefferson Medical College, Philadelphia, Pennsylvania 19107, USA.
Neuron. 1996 Jan;16(1):113-22. doi: 10.1016/s0896-6273(00)80028-8.
Voltage-dependent movement of a sodium channel S4 segment was examined by cysteine scanning mutagenesis and testing accessibility of the residues to hydrophilic cysteine-modifying reagents. These experiments indicate that 2 charged S4 residues move completely from an internally accessible to an externally accessible location in response to depolarization by passage through a short "channel" in the protein. The energetic problems of S4 movement have thus been solved in the same way that may ion channels achieve highly selective and rapid ion permeation through an open pore, by restricting the contact region between the permion and its channel.
通过半胱氨酸扫描诱变和测试残基对亲水性半胱氨酸修饰试剂的可及性,研究了钠通道S4片段的电压依赖性移动。这些实验表明,2个带电荷的S4残基通过蛋白质中的一个短“通道”传递,响应去极化时,从内部可及位置完全移动到外部可及位置。因此,S4移动的能量问题已通过与许多离子通道使离子通过开放孔实现高度选择性和快速渗透相同的方式得到解决,即通过限制通透离子与其通道之间的接触区域。