@article {69709,
	title = {In vivo multiplex imaging of dynamic neurochemical networks with designed far-red dopamine sensors},
	journal = {bioRxiv},
	year = {2024},
	month = {12/2024},
	abstract = {<p>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.Competing Interest StatementThe authors have declared no competing interest.</p>
},
	doi = {10.1101/2024.12.22.629999},
	url = {https://www.biorxiv.org/content/early/2024/12/23/2024.12.22.629999},
	author = {Zheng, Yu and Cai, Ruyi and Wang, Kui and Zhang, Junwei and Zhuo, Yizhou and Dong, Hui and Zhang, Yuqi and Wang, Yifan and Deng, Fei and Ji, En and Cui, Yiwen and Fang, Shilin and Zhang, Xinxin and Zhang, Kecheng and Wang, Jinxu and Li, Guochuan and Miao, Xiaolei and Wang, Zhenghua and Yang, Yuqing and Li, Shaochuang and Grimm, Jonathan and Johnsson, Kai and Schreiter, Eric and Lavis, Luke and Chen, Zhixing and Mu, Yu and Li, Yulong}
}
@article {47084,
	title = {Green-to-red photoconversion of GCaMP.},
	journal = {PLoS One},
	volume = {10},
	year = {2015},
	month = {2015 Sep 18},
	pages = {e0138127},
	abstract = {<p>Genetically encoded calcium indicators (GECIs) permit imaging intracellular calcium transients. Among GECIs, the GFP-based GCaMPs are the most widely used because of their high sensitivity and rapid response to changes in intracellular calcium concentrations. Here we report that the fluorescence of GCaMPs-including GCaMP3, GCaMP5 and GCaMP6-can be converted from green to red following exposure to blue-green light (450-500 nm). This photoconversion occurs in both insect and mammalian cells and is enhanced in a low oxygen environment. The red fluorescent GCaMPs retained calcium responsiveness, albeit with reduced sensitivity. We identified several amino acid residues in GCaMP important for photoconversion and generated a GCaMP variant with increased photoconversion efficiency in cell culture. This light-induced spectral shift allows the ready labeling of specific, targeted sets of GCaMP-expressing cells for functional imaging in the red channel. Together, these findings indicate the potential for greater utility of existing GCaMP reagents, including transgenic animals.</p>
},
	issn = {1932-6203},
	doi = {10.1371/journal.pone.0138127},
	author = {Ai, Minrong and Mills, Holly and Kanai, Makoto and Lai, Jason and Deng, Jingjing and Schreiter, Eric and Looger, Loren and Neubert, Thomas and Suh, Greg}
}
