Howard Hughes Medical Institute, Janelia Research Campus, Ashburn, United States.
Elife. 2020 Sep 15;9:e57249. doi: 10.7554/eLife.57249.
Understanding how the brain encodes and processes information requires the recording of neural activity that underlies different behaviors. Recent efforts in fluorescent protein engineering have succeeded in developing powerful tools for visualizing neural activity, in general by coupling neural activity to different properties of a fluorescent protein scaffold. Here, we take advantage of a previously unexploited class of reversibly switchable fluorescent proteins to engineer a new type of calcium sensor. We introduce rsCaMPARI, a genetically encoded calcium marker engineered from a reversibly switchable fluorescent protein that enables spatiotemporally precise marking, erasing, and remarking of active neuron populations under brief, user-defined time windows of light exposure. rsCaMPARI photoswitching kinetics are modulated by calcium concentration when illuminating with blue light, and the fluorescence can be reset with violet light. We demonstrate the utility of rsCaMPARI for marking and remarking active neuron populations in freely swimming zebrafish.
理解大脑如何对信息进行编码和处理需要记录潜在不同行为的神经活动。最近在荧光蛋白工程方面的努力成功地开发了用于可视化神经活动的强大工具,通常是通过将神经活动与荧光蛋白支架的不同性质偶联来实现。在这里,我们利用以前未被开发的一类可反向切换的荧光蛋白来设计一种新型的钙传感器。我们引入了 rsCaMPARI,这是一种从可反向切换的荧光蛋白工程改造而来的基因编码钙标记物,它能够在短暂的、用户定义的光暴露时间窗口内对活跃神经元群体进行时空精确的标记、擦除和重新标记。当用蓝光照射时,rsCaMPARI 的光开关动力学受钙离子浓度的调节,而荧光可以用紫光重置。我们证明了 rsCaMPARI 用于标记和重新标记自由游动斑马鱼中活跃神经元群体的效用。