Yadav Rohit, Pfeffermann Juergen, Goessweiner-Mohr Nikolaus, Glasnov Toma, Akimov Sergey A, Pohl Peter
Institute of Biophysics, Johannes Kepler University Linz, 4040 Linz, Austria.
Institute of Chemistry, Karl-Franzens-University, 8010 Graz, Austria.
Biomolecules. 2025 May 21;15(5):744. doi: 10.3390/biom15050744.
Voltage-gated potassium (Kv) channels are e ssential for shaping action potentials and rely on anionic lipids for proper gating, yet the mechanistic basis of lipid-channel interactions remains unclear. Cryo-electron microscopy studies suggest that, in the down state, arginine residues of the voltage sensor draw lipid phosphates upward, leading to a local membrane thinning of ~5 Å-an effect absent in the open state. To test whether membrane thickness directly affects voltage sensor function, we reconstituted Kv channels from (KvAP) into planar lipid bilayers containing photoswitchable lipids. Upon blue light illumination, the membrane thickened, and KvAP activity increased; UV light reversed both effects. Our findings indicate that membrane thickening weakens the interaction between lipid phosphates and voltage-sensing arginines in the down state, lowering the energy barrier for the transition to the up state and thereby promoting channel opening. This non-genetic, membrane-mediated approach provides a new strategy to control ion channel activity using light and establishes a direct, reversible link between membrane mechanics and voltage sensing, with potential applications in the remote control of neuronal excitability.
电压门控钾离子(Kv)通道对于动作电位的形成至关重要,且其正常门控依赖于阴离子脂质,然而脂质与通道相互作用的机制基础仍不清楚。冷冻电子显微镜研究表明,在关闭状态下,电压感受器的精氨酸残基将脂质磷酸基团向上牵拉,导致局部膜变薄约5埃——这一效应在开放状态下不存在。为了测试膜厚度是否直接影响电压感受器功能,我们将来自(KvAP)的Kv通道重组到含有光开关脂质的平面脂质双分子层中。蓝光照射后,膜增厚,KvAP活性增加;紫外线则逆转了这两种效应。我们的研究结果表明,膜增厚会削弱关闭状态下脂质磷酸基团与电压感受精氨酸之间的相互作用,降低向开放状态转变的能垒,从而促进通道开放。这种非基因的、膜介导的方法提供了一种利用光控制离子通道活性的新策略,并在膜力学与电压感受之间建立了直接、可逆的联系,在远程控制神经元兴奋性方面具有潜在应用。