In vivo multiplex imaging of dynamic neurochemical networks with designed far-red dopamine sensors
Yu Rong ZhengiD, Ruyi CaiiD, Kui WangiD, Junwei ZhangiD, Yizhou ZhuoiD, Hui DongiD, Yuqi ZhangiD, Yifan WangiD, Fei DengiD, En JiiD, Yiwen CuiiD, Shilin FangiD, Xinxin ZhangiD, Haiyun HuangiD, Kecheng ZhangiD, Jinxu WangiD, Guochuan LiiD, Xiaolei MiaoiD, Zhenghua WangiD, Yuqing YangiD, Shaochuang Li, Jonathan B. GrimmiD, Kai JohnssoniD, Eric R. SchreiteriD, Luke D. LavisiD, , Yulong LiiD
Abstract
Neurochemical signals like dopamine (DA) play a crucial role in a variety of brain functions through intricate interactions with other neuromodulators and intracellular signaling pathways. However, studying these complex networks has been hindered by the challenge of detecting multiple neurochemicals in vivo simultaneously. To overcome this limitation, we developed a single-protein chemigenetic DA sensor, HaloDA1.0, which combines a cpHaloTag-chemical dye approach with the G protein-coupled receptor activation-based (GRAB) strategy, providing high sensitivity for DA, sub-second response kinetics, and an extensive spectral range from far-red to near-infrared. When used together with existing green and red fluorescent neuromodulator sensors, Ca2+ indicators, cAMP sensors, and optogenetic tools, HaloDA1.0 provides high versatility for multiplex imaging in cultured neurons, brain slices, and behaving animals, facilitating in-depth studies of dynamic neurochemical networks.
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