Department of Applied Physics, Science for Life Laboratory, KTH Royal Institute of Technology, Stockholm, Sweden.
Department of Biochemistry and Biophysics, Science for Life Laboratory, Stockholm University, Stockholm, Sweden.
J Gen Physiol. 2018 Oct 1;150(10):1444-1458. doi: 10.1085/jgp.201812086. Epub 2018 Aug 27.
Voltage-sensitive membrane proteins are united by their ability to transform changes in membrane potential into mechanical work. They are responsible for a spectrum of physiological processes in living organisms, including electrical signaling and cell-cycle progression. Although the mechanism of voltage-sensing has been well characterized for some membrane proteins, including voltage-gated ion channels, even the location of the voltage-sensing elements remains unknown for others. Moreover, the detection of these elements by using experimental techniques is challenging because of the diversity of membrane proteins. Here, we provide a computational approach to predict voltage-sensing elements in any membrane protein, independent of its structure or function. It relies on an estimation of the propensity of a protein to respond to changes in membrane potential. We first show that this property correlates well with voltage sensitivity by applying our approach to a set of voltage-sensitive and voltage-insensitive membrane proteins. We further show that it correctly identifies authentic voltage-sensitive residues in the voltage-sensor domain of voltage-gated ion channels. Finally, we investigate six membrane proteins for which the voltage-sensing elements have not yet been characterized and identify residues and ions that might be involved in the response to voltage. The suggested approach is fast and simple and enables a characterization of voltage sensitivity that goes beyond mere identification of charges. We anticipate that its application before mutagenesis experiments will significantly reduce the number of potential voltage-sensitive elements to be tested.
电压门控膜蛋白的共同特点是能够将膜电位的变化转化为机械功。它们负责生物体的一系列生理过程,包括电信号和细胞周期进程。尽管已经很好地描述了一些膜蛋白(包括电压门控离子通道)的电压感应机制,但对于其他膜蛋白,甚至电压感应元件的位置仍不清楚。此外,由于膜蛋白的多样性,使用实验技术检测这些元件具有挑战性。在这里,我们提供了一种计算方法,可以预测任何膜蛋白中的电压感应元件,而无需考虑其结构或功能。它依赖于对蛋白质响应膜电位变化的倾向的估计。我们首先通过将我们的方法应用于一组电压敏感和电压不敏感的膜蛋白来证明该特性与电压敏感性密切相关。我们进一步表明,它可以正确识别电压门控离子通道电压传感器域中的真实电压敏感残基。最后,我们研究了六个尚未确定电压感应元件的膜蛋白,并确定了可能参与电压响应的残基和离子。所提出的方法快速简单,能够对电压敏感性进行特征描述,而不仅仅是识别电荷。我们预计,在进行诱变实验之前,该方法的应用将大大减少需要测试的潜在电压敏感元件的数量。