Bright and stable luminescent probes for target engagement profiling in live cells

被引:38
作者
Payne, N. Connor [1 ,2 ]
Kalyakina, Alena S. [1 ,3 ]
Singh, Kritika [1 ,4 ]
Tye, Mark A. [1 ,5 ]
Mazitschek, Ralph [1 ,6 ,7 ]
机构
[1] Massachusetts Gen Hosp, Ctr Syst Biol, Boston, MA 02114 USA
[2] Harvard Univ, Dept Chem & Chem Biol, Cambridge, MA 02138 USA
[3] Karlsruhe Inst Technol, Inst Organ Chem, Karlsruhe, Germany
[4] Northeastern Univ, Dept Bioengn, Boston, MA 02115 USA
[5] Harvard Grad Sch Arts & Sci, Cambridge, MA USA
[6] Harvard TH Chan Sch Publ Hlth, Boston, MA 02115 USA
[7] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
FRET; LIGAND; TERBIUM; DEGRADATION; INHIBITORS; COMPLEXES; EUROPIUM; ASSAYS;
D O I
10.1038/s41589-021-00877-5
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
CoraFluors, a class of macrocyclic terbium complexes for use in time-resolved FRET, exhibit physicochemical properties desirable for biological studies, including characterization of Keap1 ligands and HDAC1 target engagement profiling in live cells. The pace of progress in biomedical research directly depends on techniques that enable the quantitative interrogation of interactions between proteins and other biopolymers, or with their small-molecule ligands. Time-resolved Forster resonance energy transfer (TR-FRET) assay platforms offer high sensitivity and specificity. However, the paucity of accessible and biocompatible luminescent lanthanide complexes, which are essential reagents for TR-FRET-based approaches, and their poor cellular permeability have limited broader adaptation of TR-FRET beyond homogeneous and extracellular assay applications. Here, we report the development of CoraFluors, a new class of macrotricyclic terbium complexes, which are synthetically readily accessible, stable in biological media and exhibit photophysical and physicochemical properties that are desirable for biological studies. We validate the performance of CoraFluors in cell-free systems, identify cell-permeable analogs and demonstrate their utility in the quantitative domain-selective characterization of Keap1 ligands, as well as in isoform-selective target engagement profiling of HDAC1 inhibitors in live cells.
引用
收藏
页码:1168 / 1177
页数:10
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