Lin Wenwei, 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.
ACS Med Chem Lett. 2024 Oct 28;15(11):1987-1996. doi: 10.1021/acsmedchemlett.4c00416. eCollection 2024 Nov 14.
Human constitutive androstane receptor (hCAR) regulates xenobiotic metabolism. Its large and flexible ligand binding pocket can accommodate structurally diverse compounds. An assay for characterizing the binding of ligands to hCAR is needed but has not been reported. Here, we first discovered the promiscuous kinase inhibitor SNS-032 and its derivative THAL-SNS-032 as binders of hCAR, then developed BODIPY FL SNS 032 () as a high-affinity hCAR fluorescent probe ( : 300 ± 30 nM) in a TR-FRET binding assay and used it to characterize hCAR ligands for their competitive binding activities. BODIPY FL SNS 032 also displayed high binding affinities to multiple kinases, such as hGSK3A ( : 4.5 ± 0.2 nM), hCDK9/CycT1 ( : 5.1 ± 0.6 nM), hMAPK15 ( : 340 ± 20 nM), hCASK ( : 550 ± 30 nM), and hCAMKK2 ( : 530 ± 40 nM). BODIPY FL SNS 032 is therefore a versatile probe for hCAR and multiple kinases.
人组成型雄甾烷受体(hCAR)调节外源性物质的代谢。其大而灵活的配体结合口袋可以容纳结构多样的化合物。目前需要一种用于表征配体与hCAR结合的分析方法,但尚未见报道。在此,我们首先发现了多激酶抑制剂SNS - 032及其衍生物THAL - SNS - 032作为hCAR的结合剂,然后在时间分辨荧光共振能量转移(TR - FRET)结合分析中开发了BODIPY FL SNS 032(解离常数:300±30 nM)作为一种高亲和力的hCAR荧光探针,并使用它来表征hCAR配体的竞争结合活性。BODIPY FL SNS 032对多种激酶也表现出高结合亲和力,如人糖原合成酶激酶3A(hGSK3A,解离常数:4.5±0.2 nM)、人周期蛋白依赖性激酶9/细胞周期蛋白T1(hCDK9/CycT1,解离常数:5.1±0.6 nM)、人丝裂原活化蛋白激酶15(hMAPK15,解离常数:340±20 nM)、人钙/钙调蛋白依赖性丝氨酸蛋白激酶(hCASK,解离常数:550±30 nM)和人钙调蛋白依赖性蛋白激酶激酶2(hCAMKK2,解离常数:530±40 nM)。因此,BODIPY FL SNS 032是一种用于hCAR和多种激酶的通用探针。