Department of Pediatrics and Institute for Molecular Pediatric Sciences, University of Chicago, Chicago, IL 60615, USA.
Sci Signal. 2011 Jul 26;4(184):pe35. doi: 10.1126/scisignal.2002225.
New evidence reveals that the common electrolyte disorder hypokalemia can induce K2P1 channels that are normally selective for K+ to break the rules and conduct Na+. This defiant behavior leads to paradoxical depolarization of many cells in the heart, increasing the risk for lethal arrhythmia. The new research resolves a mystery uncovered 50 years ago and bestows an array of new riddles. Here, I discuss how K2P1 might achieve this alchemy--through stable residence of the K+ selectivity filter in a Na+-conductive state between its open and C-inactive configurations--and predict that other K+ channels and environmental stimuli will be discovered to produce the same excitatory misconduct.
新证据表明,常见的电解质紊乱低钾血症可诱导通常对 K+具有选择性的 K2P1 通道打破规则并传导 Na+。这种挑衅行为导致心脏中许多细胞发生反常去极化,增加致命性心律失常的风险。这项新研究解决了 50 年前发现的一个谜团,并带来了一系列新的谜题。在这里,我将讨论 K2P1 如何通过其开放和 C 失活构象之间的 Na+传导状态下的 K+选择性过滤器的稳定驻留来实现这种炼金术,并预测将发现其他 K+通道和环境刺激因素会产生相同的兴奋性失常行为。