Kv7.1 ion channels require a lipid to couple voltage sensing to pore opening

被引:149
作者
Zaydman, Mark A. [1 ]
Silva, Jonathan R. [1 ]
Delaloye, Kelli [1 ]
Li, Yang [1 ]
Liang, Hongwu [1 ]
Larsson, H. Peter [2 ]
Shi, Jingyi [1 ]
Cui, Jianmin [1 ]
机构
[1] Washington Univ, Dept Biomed Engn, Ctr Invest Membrane Excitabil Dis, Cardiac Bioelect & Arrhythmia Ctr, St Louis, MO 63130 USA
[2] Univ Miami, Miller Sch Med, Dept Physiol & Biophys, Miami, FL 33136 USA
基金
美国国家卫生研究院;
关键词
channelopathy; electromechanical coupling; KCNQ; voltage channel; phosphoinositide; LONG-QT SYNDROME; GATED SODIUM-CHANNEL; DEPENDENT K+ CHANNEL; POTASSIUM CHANNEL; I-KS; CRYSTAL-STRUCTURE; PHOSPHATIDYLINOSITOL 4,5-BISPHOSPHATE; ELECTROSTATIC INTERACTIONS; STRUCTURAL BASIS; SYNDROME GENES;
D O I
10.1073/pnas.1305167110
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Voltage-gated ion channels generate dynamic ionic currents that are vital to the physiological functions of many tissues. These proteins contain separate voltage-sensing domains, which detect changes in transmembrane voltage, and pore domains, which conduct ions. Coupling of voltage sensing and pore opening is critical to the channel function and has been modeled as a protein-protein interaction between the two domains. Here, we show that coupling in Kv7.1 channels requires the lipid phosphatidylinositol 4,5-bisphosphate (PIP2). We found that voltage-sensing domain activation failed to open the pore in the absence of PIP2. This result is due to loss of coupling because PIP2 was also required for pore opening to affect voltage-sensing domain activation. We identified a critical site for PIP2-dependent coupling at the interface between the voltage-sensing domain and the pore domain. This site is actually a conserved lipid-binding site among different K+ channels, suggesting that lipids play an important role in coupling in many ion channels.
引用
收藏
页码:13180 / 13185
页数:6
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