Abdelfattah Ahmed S, Farhi Samouil L, Zhao Yongxin, Brinks Daan, Zou Peng, Ruangkittisakul Araya, Platisa Jelena, Pieribone Vincent A, Ballanyi Klaus, Cohen Adam E, Campbell Robert E
Department of Chemistry, University of Alberta, Edmonton, Alberta T6G 2G2, Canada.
Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138.
J Neurosci. 2016 Feb 24;36(8):2458-72. doi: 10.1523/JNEUROSCI.3484-15.2016.
Optical imaging of voltage indicators based on green fluorescent proteins (FPs) or archaerhodopsin has emerged as a powerful approach for detecting the activity of many individual neurons with high spatial and temporal resolution. Relative to green FP-based voltage indicators, a bright red-shifted FP-based voltage indicator has the intrinsic advantages of lower phototoxicity, lower autofluorescent background, and compatibility with blue-light-excitable channelrhodopsins. Here, we report a bright red fluorescent voltage indicator (fluorescent indicator for voltage imaging red; FlicR1) with properties that are comparable to the best available green indicators. To develop FlicR1, we used directed protein evolution and rational engineering to screen libraries of thousands of variants. FlicR1 faithfully reports single action potentials (∼3% ΔF/F) and tracks electrically driven voltage oscillations at 100 Hz in dissociated Sprague Dawley rat hippocampal neurons in single trial recordings. Furthermore, FlicR1 can be easily imaged with wide-field fluorescence microscopy. We demonstrate that FlicR1 can be used in conjunction with a blue-shifted channelrhodopsin for all-optical electrophysiology, although blue light photoactivation of the FlicR1 chromophore presents a challenge for applications that require spatially overlapping yellow and blue excitation.
基于绿色荧光蛋白(FPs)或古紫质的电压指示剂的光学成像已成为一种强大的方法,可用于以高空间和时间分辨率检测许多单个神经元的活动。相对于基于绿色FP的电压指示剂,基于红移FP的明亮电压指示剂具有光毒性较低、自发荧光背景较低以及与蓝光可激发的通道视紫红质兼容的固有优势。在这里,我们报告了一种明亮的红色荧光电压指示剂(用于电压成像红色的荧光指示剂;FlicR1),其性能与现有的最佳绿色指示剂相当。为了开发FlicR1,我们使用定向蛋白质进化和合理工程来筛选数千个变体的文库。FlicR1在单次试验记录中忠实地报告单个动作电位(约3%ΔF/F),并跟踪解离的Sprague Dawley大鼠海马神经元中100 Hz的电驱动电压振荡。此外,FlicR1可以很容易地用宽场荧光显微镜成像。我们证明FlicR1可以与蓝移通道视紫红质一起用于全光学电生理学,尽管FlicR1生色团的蓝光光激活对需要空间重叠黄色和蓝色激发的应用提出了挑战。