Xie Lai-Hua, John Scott A, Ribalet Bernard, Weiss James N
Cardiovascular Research Laboratory, Department of Medicine, David Geffen School of Medicine at UCLA, 675 Young Drive South, MRL 3645, Los Angeles, CA 90095, USA.
J Physiol. 2004 Nov 15;561(Pt 1):159-68. doi: 10.1113/jphysiol.2004.072330. Epub 2004 Sep 30.
Inward rectifier K(+) channels commonly exhibit long openings (slow gating) punctuated by rapid open-close transitions (fast gating), suggesting that two separate gates may control channel open-closed transitions. Previous studies have suggested possible gate locations at the selectivity filter and at the 'bundle crossing', where the two transmembrane segments (M1 and M2) cross near the cytoplasmic end of the pore. Wild-type Kir2.1 channels exhibit only slow gating, but mutations in the cytoplasmic pore domain at E224 and E299 have been shown to induce fast flickery gating. Since these mutations also affect polyamine affinity, we conjectured that the fast gating mechanism might affect the kinetics of polyamine block/unblock if located more intracellularly than the polyamine blocking site in the pore. Neutralization of either E224 or E299 induced fast gating and slowed both block and unblock rates by the polyamine diamine 10. The slowing of polyamine block/unblock was partly relieved by raising pH from 7.2 to 9.0, which also slowed fast gating kinetics. These findings indicate that the fast flickery gate is located intracellularly with respect to the polyamine pore-plugging site near D172, thereby excluding the selectivity filter, and implicating the bundle crossing or more intracellular site as the gate. As additional proof, fast gating induced at the selectivity filter by disrupting P loop salt bridges in WT-E138D-E138D-WT tandem had no effect on polyamine block and unblock rates. The pH sensitivity of fast gating in E224 and E299 mutants was attributed to the protonation state of H226, since the double mutant E224Q/H226K induced fast gating which was pH insensitive. Moreover, introducing a negative charge in the 224-226 region was sufficient to prevent fast gating, since the double mutant E224Q/H226E rescued wild-type Kir2.1 slow gating. These observations implicate E224 and E299 as allosteric modulators of a fast gate, located at the bundle crossing or below in Kir2.1 channels. By suppressing fast gating, these negative charges facilitate polyamine block and unblock, which may be their physiologically important role.
内向整流钾通道通常表现出长时开放(慢门控),其间穿插着快速的开闭转换(快门控),这表明可能有两个独立的门控机制控制通道的开闭转换。先前的研究表明,可能的门控位置在选择性过滤器和“束状交叉点”,即两个跨膜片段(M1和M2)在孔道胞质端附近交叉的位置。野生型Kir2.1通道仅表现出慢门控,但已证明在胞质孔道结构域的E224和E299位点发生突变会诱导快速闪烁门控。由于这些突变也会影响多胺亲和力,我们推测,如果快速门控机制位于孔道中比多胺阻断位点更靠细胞内侧的位置,那么它可能会影响多胺阻断/解除阻断的动力学。中和E224或E299中的任何一个都会诱导快速门控,并减缓多胺二胺10的阻断和解除阻断速率。将pH从7.2提高到9.0可部分缓解多胺阻断/解除阻断的减慢,这也减缓了快速门控动力学。这些发现表明,快速闪烁门控相对于D172附近的多胺孔道堵塞位点位于细胞内侧,从而排除了选择性过滤器,并暗示束状交叉点或更靠细胞内侧的位点是门控位置。作为进一步的证据,通过破坏WT-E138D-E138D-WT串联体中的P环盐桥在选择性过滤器处诱导的快速门控对多胺阻断和解除阻断速率没有影响。E224和E299突变体中快速门控的pH敏感性归因于H226的质子化状态,因为双突变体E224Q/H226K诱导的快速门控对pH不敏感。此外,在224-226区域引入负电荷足以阻止快速门控,因为双突变体E224Q/H226E恢复了野生型Kir2.1的慢门控。这些观察结果表明E224和E299是位于Kir2.1通道束状交叉点或其下方的快速门控的变构调节剂。通过抑制快速门控,这些负电荷促进了多胺的阻断和解除阻断,这可能是它们在生理上的重要作用。