受体
生物正交化学
神经递质受体
内生
神经科学
神经递质
生物
谷氨酸受体
生物化学
化学
细胞生物学
组合化学
点击化学
作者
Hiroshi Nonaka,Seiji Sakamoto,Kazuki Shiraiwa,Mamoru Ishikawa,Tomonori Tamura,Kyohei Okuno,Takumi Kondo,Shigeki Kiyonaka,Etsuo A. Susaki,Chika Shimizu,Hiroki R. Ueda,Wataru Kakegawa,Itaru Arai,Michisuke Yuzaki,Itaru Hamachi
标识
DOI:10.1073/pnas.2313887121
摘要
Neurotransmitter receptors are essential components of synapses for communication between neurons in the brain. Because the spatiotemporal expression profiles and dynamics of neurotransmitter receptors involved in many functions are delicately governed in the brain, in vivo research tools with high spatiotemporal resolution for receptors in intact brains are highly desirable. Covalent labeling by chemical reaction (chemical labeling) of proteins without genetic manipulation is now a powerful method for analyzing receptors in vitro. However, selective target receptor labeling in the brain has not yet been achieved. This study shows that ligand-directed alkoxyacylimidazole (LDAI) chemistry can be used to selectively tether synthetic probes to target endogenous receptors in living mouse brains. The reactive LDAI reagents with negative charges were found to diffuse well over the whole brain and could selectively label target endogenous receptors, including AMPAR, NMDAR, mGlu1, and GABA A R. This simple and robust labeling protocol was then used for various applications: three-dimensional spatial mapping of endogenous receptors in the brains of healthy and disease-model mice; multi-color receptor imaging; and pulse–chase analysis of the receptor dynamics in postnatal mouse brains. Here, results demonstrated that bioorthogonal receptor modification in living animal brains may provide innovative molecular tools that contribute to the in-depth understanding of complicated brain functions.
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