生物
原位
体内
药物发现
细胞生物学
计算生物学
细胞
药品
鉴定(生物学)
亚细胞定位
生物物理学
生物化学
细胞质
遗传学
药理学
化学
有机化学
植物
作者
Zhengyuan Pang,Michael A. Schafroth,Daisuke Ogasawara,Yu Wang,Victoria Nudell,Neeraj K. Lal,Dong Uk Yang,Kristina Wang,Dylan M. Herbst,Jacquelyn Ha,Carlos Guijas,Jacqueline L. Blankman,Benjamin F. Cravatt,Ye Li
出处
期刊:Cell
[Elsevier]
日期:2022-05-01
卷期号:185 (10): 1793-1805.e17
被引量:29
标识
DOI:10.1016/j.cell.2022.03.040
摘要
The lack of tools to observe drug-target interactions at cellular resolution in intact tissue has been a major barrier to understanding in vivo drug actions. Here, we develop clearing-assisted tissue click chemistry (CATCH) to optically image covalent drug targets in intact mammalian tissues. CATCH permits specific and robust in situ fluorescence imaging of target-bound drug molecules at subcellular resolution and enables the identification of target cell types. Using well-established inhibitors of endocannabinoid hydrolases and monoamine oxidases, direct or competitive CATCH not only reveals distinct anatomical distributions and predominant cell targets of different drug compounds in the mouse brain but also uncovers unexpected differences in drug engagement across and within brain regions, reflecting rare cell types, as well as dose-dependent target shifts across tissue, cellular, and subcellular compartments that are not accessible by conventional methods. CATCH represents a valuable platform for visualizing in vivo interactions of small molecules in tissue.
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