Lin Xianming, Veenstra Richard D
Department of Pharmacology, The State University of New York Upstate Medical University, Syracuse, New York 13210, USA.
Biophys J. 2007 Jul 15;93(2):483-95. doi: 10.1529/biophysj.106.098517. Epub 2007 Apr 27.
Spermine inhibits rat connexin40 (Cx40) gap junctions. Glutamate residues at positions 9 and 13 and a basic amino acid (HKH) motif at positions 15-17 on the amino terminal domain are essential for this inhibitory activity. Questions remain as to whether spermine occludes the channel within the ion permeation pathway. To examine this question, cis or trans [KCl] was systematically lowered and the equilibrium dissociation constants (K(d)) and kinetics of unilateral spermine block on wild-type Cx40 gap junctions were determined. Asymmetric reductions in the trans [KCl] produced noticeable asymmetric shifts in the V(1/2) and G(min) values that progressively resembled G(j)-V(j) relationships observed in heterotypic connexin gap junction combinations. As cis or trans [KCl] was reduced by 25%, 50%, or 75% relative to the spermine-containing side, the transjunctional voltage (V(j))-dependent K(d) values increased or decreased, respectively. The spermine on-rates and off-rates, calculated from the junctional current decay and recovery time constants, were similarly affected. Hill coefficients for the spermine dose-response curves were approximately 0.58, indicative of negative cooperativity and possible multiple spermine inhibitory sites. The equivalent "electrical distance" (delta) ranged from 0.61 at 25% cis [KCl] to 1.4 at 25% trans [KCl], with a Hill coefficient of 1.0. Symmetrical reductions in [KCl] resulted in intermediate decreases in the spermine K(d)s, indicative of a minor electrostatic effect and a more significant effect of the transjunctional KCl electrodiffusion potential on the spermine association and dissociation rates. These data are consistent with a single spermine molecule being sufficient to occlude the Cx40 gap junction channel within the KCl permeation pathway.
精胺抑制大鼠连接蛋白40(Cx40)间隙连接。氨基末端结构域第9和13位的谷氨酸残基以及第15 - 17位的碱性氨基酸(HKH)基序对于这种抑制活性至关重要。关于精胺是否在离子渗透途径内阻塞通道仍存在疑问。为了研究这个问题,系统地降低顺式或反式[KCl]浓度,并测定野生型Cx40间隙连接上单侧精胺阻断的平衡解离常数(K(d))和动力学。反式[KCl]的不对称降低在V(1/2)和G(min)值上产生了明显的不对称变化,逐渐类似于在异型连接蛋白间隙连接组合中观察到的G(j)-V(j)关系。当顺式或反式[KCl]相对于含精胺侧降低25%、50%或75%时,跨连接电压(V(j))依赖性K(d)值分别增加或降低。根据连接电流衰减和恢复时间常数计算的精胺结合速率和解离速率也受到类似影响。精胺剂量反应曲线的希尔系数约为0.58,表明存在负协同性和可能的多个精胺抑制位点。等效“电距离”(δ)范围从25%顺式[KCl]时的0.61到25%反式[KCl]时的1.4,希尔系数为1.0。[KCl]浓度的对称降低导致精胺K(d)值出现中等程度下降,表明存在较小的静电效应以及跨连接KCl电扩散电位对精胺结合和解离速率有更显著的影响。这些数据与单个精胺分子足以在KCl渗透途径内阻塞Cx40间隙连接通道的观点一致。