Tinker A, Williams A J
Department of Cardiac Medicine, National Heart and Lung Institute, University of London, England.
Biophys J. 1993 Oct;65(4):1678-83. doi: 10.1016/S0006-3495(93)81201-3.
We have reported that the large impermeant organic cations tetrabutyl ammonium (TBA+), tetrapentyl ammonium, and the charged local anesthetic QX314 produce unique reduced conductance states in the purified sheep cardiac sarcoplasmic reticulum Ca2+ release channel when present at the cytoplasmic face of the channel. We have interpreted this as a form of partial occlusion by the blocking cation in wide vestibules of the conduction pathway. Following modification with ryanodine, which causes the channel to enter a reduced conductance state with long open dwell time, these cations block the receptor channel to a level that is indistinguishable from the closed state. The voltage dependence of TBA+'s interaction with the Ca2+ release channel is the same before and after ryanodine modification. The concentration dependence is different, in that the ryanodine-modified channel has one-third the affinity for TBA+, which is accounted for predominantly by changes in the TBA+ on rate. The data are compatible with a structural change in the vestibule of the conduction pathway consequent upon ryanodine binding that reduces the capture radius for blocking ion entry.
我们曾报道,当大的非渗透性有机阳离子四丁基铵(TBA+)、四戊基铵以及带电荷的局部麻醉药QX314存在于通道的胞质面时,它们会在纯化的绵羊心肌肌浆网Ca2+释放通道中产生独特的电导降低状态。我们将此解释为传导通路宽阔前庭中的阻断阳离子造成的一种部分阻塞形式。在用ryanodine修饰后,通道进入具有长开放驻留时间的电导降低状态,这些阳离子将受体通道阻断至与关闭状态无法区分的水平。ryanodine修饰前后,TBA+与Ca2+释放通道相互作用的电压依赖性相同。浓度依赖性不同,因为经ryanodine修饰的通道对TBA+的亲和力是未修饰通道的三分之一,这主要是由TBA+结合速率的变化所致。这些数据与ryanodine结合后传导通路前庭的结构变化相符,该变化减小了阻断离子进入的捕获半径。