Department of Biomedical Engineering, Cardiac Bioelectricity and Arrhythmia Center, Washington University in St. Louis, St. Louis, MO 63130-4862, USA.
Proc Natl Acad Sci U S A. 2013 Aug 6;110(32):13180-5. doi: 10.1073/pnas.1305167110. Epub 2013 Jul 16.
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.
电压门控离子通道产生动态离子电流,对许多组织的生理功能至关重要。这些蛋白质包含独立的电压感应结构域,用于检测跨膜电压的变化,以及孔道结构域,用于传导离子。电压感应和孔道开放的偶联对通道功能至关重要,已被建模为两个结构域之间的蛋白质-蛋白质相互作用。在这里,我们表明 Kv7.1 通道的偶联需要脂质磷脂酰肌醇 4,5-二磷酸(PIP2)。我们发现,在没有 PIP2 的情况下,电压感应结构域的激活无法打开孔道。这一结果是由于偶联的丧失所致,因为 PIP2 也需要打开孔道以影响电压感应结构域的激活。我们确定了位于电压感应结构域和孔道结构域之间界面处的一个关键的 PIP2 依赖性偶联位点。该位点实际上是不同 K(+)通道之间的一个保守的脂质结合位点,表明脂质在许多离子通道的偶联中发挥重要作用。