Aiyar J, Withka J M, Rizzi J P, Singleton D H, Andrews G C, Lin W, Boyd J, Hanson D C, Simon M, Dethlefs B
Department of Physiology and Biophysics, University of California, Irvine 92717, USA.
Neuron. 1995 Nov;15(5):1169-81. doi: 10.1016/0896-6273(95)90104-3.
The architecture of the pore-region of a voltage-gated K+ channel, Kv1.3, was probed using four high affinity scorpion toxins as molecular calipers. We established the structural relatedness of these toxins by solving the structures of kaliotoxin and margatoxin and comparing them with the published structure of charybdotoxin; a homology model of noxiustoxin was then developed. Complementary mutagenesis of Kv1.3 and these toxins, combined with electrostatic compliance and thermodynamic mutant cycle analyses, allowed us to identify multiple toxin-channel interactions. Our analyses reveal the existence of a shallow vestibule at the external entrance to the pore. This vestibule is approximately 28-32 A wide at its outer margin, approximately 28-34 A wide at its base, and approximately 4-8 A deep. The pore is 9-14 A wide at its external entrance and tapers to a width of 4-5 A at a depth of approximately 5-7 A from the vestibule. This structural information should directly aid in developing topological models of the pores of related ion channels and facilitate therapeutic drug design.
利用四种高亲和力蝎毒素作为分子卡尺,对电压门控钾通道Kv1.3的孔区结构进行了探测。我们通过解析卡利毒素和边缘毒素的结构,并将它们与已发表的章鱼毒素结构进行比较,确定了这些毒素的结构相关性;随后构建了诺毒素的同源模型。对Kv1.3和这些毒素进行互补诱变,结合静电顺应性和热力学突变循环分析,使我们能够确定多种毒素-通道相互作用。我们的分析揭示了孔外部入口处存在一个浅前庭。这个前庭外缘宽约28-32埃,底部宽约28-34埃,深约4-8埃。孔的外部入口宽9-14埃,从前庭大约5-7埃深处逐渐变窄至4-5埃宽。这些结构信息应直接有助于建立相关离子通道孔的拓扑模型,并促进治疗药物设计。