生物
体内
点击化学
同种类的
分子成像
药物发现
癌症
细胞生物学
癌症治疗
癌症治疗
生物化学
癌症研究
癌细胞
临床前影像学
小分子
阿法替尼
化学生物学
抗癌药物
计算生物学
药物开发
药品
共价键
组织分布
生物信息学
生物物理学
抗癌药
药物输送
血浆蛋白结合
组织工程
癌症生物标志物
纳米技术
作者
Zhengyuan Pang,Verina H. Leung,Cailynn C. Wang,Ahmadreza Attarpour,Anthony Rinaldi,Hanbing Shen,Maria Dolores Moya-Garzon,Logan H. Sigua,Claire Rammel,Alexandra Selke,Christopher Glynn,Melaina Yender,Senhan Xu,Javid J. Moslehi,Peng Wu,Jonathan Z. Long,Maged Goubran,Benjamin F. Cravatt,Li Ye
出处
期刊:Cell
[Cell Press]
日期:2025-12-22
卷期号:189 (3): 725-738.e15
被引量:5
标识
DOI:10.1016/j.cell.2025.11.030
摘要
As our understanding of biological systems reaches single-cell and high spatial resolutions, it becomes imperative that pharmacological approaches match this precision to understand drug actions. This need is particularly urgent for the targeted covalent inhibitors that are currently re-entering the stage for cancer treatments. By leveraging the unique kinetics of click reactions, we developed volumetric clearing-assisted tissue click chemistry (vCATCH) to enable deep and homogeneous click labeling across the three-dimensional (3D) mammalian body. With simple and passive incubation steps, vCATCH offers cellular-resolution drug imaging in the entire adult mouse. We combined vCATCH with hydrogel-based reinforcement of three-dimensional imaging solvent-cleared organs (HYBRiD) imaging and virtual reality to visualize and quantify in vivo targets of two clinical cancer drugs, afatinib and ibrutinib, which recapitulated their known pharmacological distribution and revealed previously unreported tissue and cell-type engagement potentially linked to off-target effects. vCATCH provides a body-wide, unbiased platform to map covalent drug engagements at unprecedented scale and precision.
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