Shin Hyeon-Gyu, Lu Zhe
Department of Physiology, University of Pennsylvania, Philadelphia 19104, USA.
J Gen Physiol. 2005 Apr;125(4):413-26. doi: 10.1085/jgp.200409242. Epub 2005 Mar 14.
IRK1 (Kir2.1) inward-rectifier K+ channels exhibit exceedingly steep rectification, which reflects strong voltage dependence of channel block by intracellular cations such as the polyamine spermine. On the basis of studies of IRK1 block by various amine blockers, it was proposed that the observed voltage dependence (valence approximately 5) of IRK1 block by spermine results primarily from K+ ions, not spermine itself, traversing the transmembrane electrical field that drops mostly across the narrow ion selectivity filter, as spermine and K+ ions displace one another during channel block and unblock. If indeed spermine itself only rarely penetrates deep into the ion selectivity filter, then a long blocker with head groups much wider than the selectivity filter should exhibit comparably strong voltage dependence. We confirm here that channel block by two molecules of comparable length, decane-bis-trimethylammonium (bis-QA(C10)) and spermine, exhibit practically identical overall voltage dependence even though the head groups of the former are much wider ( approximately 6 A) than the ion selectivity filter ( approximately 3 A). For both blockers, the overall equilibrium dissociation constant differs from the ratio of apparent rate constants of channel unblock and block. Also, although steady-state IRK1 block by both cations is strongly voltage dependent, their apparent channel-blocking rate constant exhibits minimal voltage dependence, which suggests that the pore becomes blocked as soon as the blocker encounters the innermost K+ ion. These findings strongly suggest the existence of at least two (potentially identifiable) sequentially related blocked states with increasing numbers of K+ ions displaced. Consequently, the steady-state voltage dependence of IRK1 block by spermine or bis-QA(C10) should increase with membrane depolarization, a prediction indeed observed. Further kinetic analysis identifies two blocked states, and shows that most of the observed steady-state voltage dependence is associated with the transition between blocked states, consistent with the view that the mutual displacement of blocker and K+ ions must occur mainly as the blocker travels along the long inner pore.
IRK1(Kir2.1)内向整流钾通道表现出极其陡峭的整流特性,这反映了细胞内阳离子(如多胺精胺)对通道阻滞的强烈电压依赖性。基于对IRK1被各种胺类阻滞剂阻滞的研究,有人提出,观察到的精胺对IRK1阻滞的电压依赖性(价态约为5)主要源于钾离子,而非精胺本身穿过主要在狭窄离子选择性过滤器上下降的跨膜电场,因为在通道阻滞和解阻过程中,精胺和钾离子会相互取代。如果精胺本身确实很少深入离子选择性过滤器,那么一种头部基团比选择性过滤器宽得多的长阻滞剂应该表现出相当强的电压依赖性。我们在此证实,两种长度相当的分子,癸烷 - 双 - 三甲基铵(双 - QA(C10))和精胺,对通道的阻滞表现出几乎相同的整体电压依赖性,尽管前者的头部基团(约6埃)比离子选择性过滤器(约3埃)宽得多。对于这两种阻滞剂,整体平衡解离常数不同于通道解阻和阻滞的表观速率常数之比。此外,尽管两种阳离子对IRK1的稳态阻滞都强烈依赖于电压,但其表观通道阻滞速率常数表现出最小的电压依赖性,这表明一旦阻滞剂遇到最内层的钾离子,孔道就会被阻塞。这些发现强烈表明存在至少两种(可能可识别的)与钾离子被取代数量增加依次相关的阻滞状态。因此,精胺或双 - QA(C10)对IRK1阻滞的稳态电压依赖性应随膜去极化而增加,这一预测确实得到了观察验证。进一步的动力学分析确定了两种阻滞状态,并表明观察到的大部分稳态电压依赖性与阻滞状态之间的转变有关,这与阻滞剂和钾离子的相互取代必须主要在阻滞剂沿着长的内部孔道移动时发生的观点一致。