Lin Wenwei, Liu Jiuyu, Jeffries Cynthia, Yang Lei, Lu Yan, Lee Richard E, Chen Taosheng
Department of Chemical Biology and Therapeutics, St. Jude Children's Research Hospital , 262 Danny Thomas Place, Mail Stop 1000, Memphis, Tennessee 38105, United States.
Bioconjug Chem. 2014 Sep 17;25(9):1664-77. doi: 10.1021/bc5002856. Epub 2014 Aug 18.
The pregnane X receptor (PXR) regulates the metabolism and excretion of xenobiotics and endobiotics by regulating the expression of drug-metabolizing enzymes and transporters. The unique structure of PXR allows it to bind many drugs and drug leads, possibly causing undesired drug-drug interactions. Therefore, it is crucial to evaluate whether chemicals or drugs bind to PXR. Fluorescence-based assays are preferred because of their sensitivity and nonradioactive nature. On the basis of our previously characterized 4 (BODIPY FL vinblastine), a high-affinity PXR probe, we developed 20 (BODIPY FL vindoline) and showed that it is a novel and potent PXR fluorescent probe with Kd of 256 nM in a time-resolved fluorescence resonance energy transfer (TR-FRET) binding assay with PXR. By using 20 (BODIPY FL vindoline) in the PXR TR-FRET assay, we obtained a more than 7-fold signal-to-background ratio and high signal stability (signal was stable for at least 120 min, and Z'-factor > 0.85 from 30 to 240 min). The assay can tolerate DMSO up to 2%. This assay has been used to evaluate a panel of PXR ligands for their PXR-binding affinities. The performance of 20 (BODIPY FL vindoline) in the PXR TR-FRET assay makes it an ideal PXR fluorescent probe, and the newly developed PXR TR-FRET assay with 20 (BODIPY FL vindoline) as a fluorescent probe is suitable for high-throughput screening to identify PXR-binding ligands.
孕烷X受体(PXR)通过调节药物代谢酶和转运蛋白的表达来调控外源性物质和内源性物质的代谢及排泄。PXR的独特结构使其能够结合多种药物及潜在药物,这可能会导致不良的药物相互作用。因此,评估化学物质或药物是否与PXR结合至关重要。基于荧光的检测方法因其灵敏度高且无放射性而更受青睐。基于我们之前鉴定的4(硼二吡咯氟化物长春碱),一种高亲和力的PXR探针,我们开发了20(硼二吡咯氟化物长春多灵),并表明它是一种新型且高效的PXR荧光探针,在与PXR的时间分辨荧光共振能量转移(TR-FRET)结合检测中,其解离常数(Kd)为256 nM。通过在PXR的TR-FRET检测中使用20(硼二吡咯氟化物长春多灵),我们获得了超过7倍的信背比以及高信号稳定性(信号至少稳定120分钟,在30至240分钟内Z'因子> 0.85)。该检测可耐受高达2%的二甲基亚砜(DMSO)。此检测方法已用于评估一组PXR配体与PXR的结合亲和力。20(硼二吡咯氟化物长春多灵)在PXR的TR-FRET检测中的性能使其成为理想的PXR荧光探针,并且以20(硼二吡咯氟化物长春多灵)作为荧光探针新开发的PXR的TR-FRET检测适用于高通量筛选以鉴定与PXR结合的配体。