An ultrasensitive biosensor for high-resolution kinase activity imaging in awake mice

被引:61
|
作者
Zhang, Jin-Fan [1 ,2 ]
Liu, Bian [3 ,4 ]
Hong, Ingie [3 ,4 ]
Mo, Albert [1 ]
Roth, Richard H. [3 ,4 ,8 ]
Tenner, Brian [1 ]
Lin, Wei [1 ]
Zhang, Jason Z. [1 ,2 ]
Molina, Rosana S. [5 ]
Drobizhev, Mikhail [5 ]
Hughes, Thomas E. [5 ]
Tian, Lin [6 ]
Huganir, Richard L. [3 ,4 ]
Mehta, Sohum [1 ]
Zhang, Jin [1 ,2 ,7 ]
机构
[1] Univ Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
[3] Johns Hopkins Univ, Sch Med, Solomon H Snyder Dept Neurosci, Baltimore, MD 21218 USA
[4] Johns Hopkins Univ, Sch Med, Kavli Neurosci Discovery Inst, Baltimore, MD 21218 USA
[5] Montana State Univ, Dept Cell Biol & Neurosci, Bozeman, MT 59717 USA
[6] Univ Calif Davis, Dept Biochem & Mol Med, Sacramento, CA 95817 USA
[7] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
[8] Stanford Univ, Sch Med, Dept Neurosurg, Palo Alto, CA 94304 USA
关键词
A ACTIVITY; FLUORESCENT PROTEINS; PHASIC DOPAMINE; CIRCUIT; PKA; ACTIVATION; PLASTICITY; RECEPTORS; NEURONS; STATE;
D O I
10.1038/s41589-020-00660-y
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Protein kinases control nearly every facet of cellular function. These key signaling nodes integrate diverse pathway inputs to regulate complex physiological processes, and aberrant kinase signaling is linked to numerous pathologies. While fluorescent protein-based biosensors have revolutionized the study of kinase signaling by allowing direct, spatiotemporally precise kinase activity measurements in living cells, powerful new molecular tools capable of robustly tracking kinase activity dynamics across diverse experimental contexts are needed to fully dissect the role of kinase signaling in physiology and disease. Here, we report the development of an ultrasensitive, second-generation excitation-ratiometric protein kinase A (PKA) activity reporter (ExRai-AKAR2), obtained via high-throughput linker library screening, that enables sensitive and rapid monitoring of live-cell PKA activity across multiple fluorescence detection modalities, including plate reading, cell sorting and one- or two-photon imaging. Notably, in vivo visual cortex imaging in awake mice reveals highly dynamic neuronal PKA activity rapidly recruited by forced locomotion.
引用
收藏
页码:39 / 46
页数:24
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