In vivo imaging of specific drug-target binding at subcellular resolution

被引:67
作者
Dubach, J. M. [1 ,2 ]
Vinegoni, C. [1 ,2 ]
Mazitschek, R. [1 ,2 ]
Fumene Feruglio, P. [1 ,2 ]
Cameron, L. A. [3 ]
Weissleder, R. [1 ,2 ]
机构
[1] Massachusetts Gen Hosp, Ctr Syst Biol, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Richard B Simches Res Ctr, Boston, MA 02114 USA
[3] Dana Farber Canc Inst, Dept Pediat Oncol, Boston, MA 02215 USA
基金
美国国家卫生研究院;
关键词
POLARIZED FLUORESCENCE MICROSCOPY; GPI-ANCHORED PROTEINS; LIVING CELLS; SINGLE-CELL; LIVE CELLS; ANISOTROPY; ENGAGEMENT; ORGANIZATION; INHIBITION; INSIGHTS;
D O I
10.1038/ncomms4946
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The possibility of measuring binding of small-molecule drugs to desired targets in live cells could provide a better understanding of drug action. However, current approaches mostly yield static data, require lysis or rely on indirect assays and thus often provide an incomplete understanding of drug action. Here, we present a multiphoton fluorescence anisotropy microscopy live cell imaging technique to measure and map drug-target interaction in real time at subcellular resolution. This approach is generally applicable using any fluorescently labelled drug and enables high-resolution spatial and temporal mapping of bound and unbound drug distribution. To illustrate our approach we measure intracellular target engagement of the chemotherapeutic Olaparib, a poly(ADP-ribose) polymerase inhibitor, in live cells and within a tumour in vivo. These results are the first generalizable approach to directly measure drug-target binding in vivo and present a promising tool to enhance understanding of drug activity.
引用
收藏
页数:9
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