Intracellular fluorescence competition assay for inhibitor engagement of histone deacetylase

被引:2
|
作者
Padilla-Coley, Sasha [1 ]
Rudebeck, Elley E. [2 ]
Smith, Bradley D. [1 ]
Pfeffer, Frederick M. [2 ]
机构
[1] Univ Notre Dame, Dept Chem & Biochem, 251 Nieuwland Sci Hall, Notre Dame, IN 46556 USA
[2] Deakin Univ, Sch Life & Environm Sci, Waurn Ponds, Vic 3216, Australia
基金
美国国家科学基金会;
关键词
Naphthalimide; Histone deacetylase; Inhibitor; Scriptaid; Fluorescence cell microscopy; Fluorescent molecular probe; PROBES; VORINOSTAT; DISCOVERY; BINDING; CANCER;
D O I
10.1016/j.bmcl.2021.128207
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
An intracellular fluorescence competition assay was developed to assess the capability of inhibitor candidates to engage histone deacetylase (HDAC) inside living cells and thus diminish cell uptake and staining by the HDACtargeted fluorescent probe APS. Fluorescence cell microscopy and flow cytometry showed that pre-incubation of living cells with candidate inhibitors led to diminished cell uptake of the fluorescent probe. The assay was effective because the fluorescent probe (APS) possessed the required performance properties, including bright fluorescence, ready membrane diffusion, selective intracellular HDAC affinity, and negligible acute cytotoxicity. The concept of an intracellular fluorescence competition assay is generalizable and has broad applicability since it obviates the requirement to use the isolated biomacromolecule target for screening of molecular candidates with target affinity.
引用
收藏
页数:6
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