Facile Synthesis of a Fluorescent Cyclosporin A Analogue To Study Cyclophilin 40 and Cyclophilin 18 Ligands

被引:11
作者
Gaali, Steffen [1 ]
Kozany, Christian [1 ]
Hoogeland, Bastiaan [1 ]
Klein, Marielle [1 ]
Hausch, Felix [1 ]
机构
[1] Max Planck Inst Psychiat, AG Chem Genom, D-80804 Munich, Germany
关键词
Cyclophilin; Cyp18; Cyp40; cyclosporin A; CsA; fluorescent analogue; fluorescence polarization assay; HEAT-SHOCK-PROTEIN; GLUCOCORTICOID-RECEPTOR; MAMMALIAN-CELLS; GENE-EXPRESSION; CANCER CELLS; IMMUNOPHILIN; FKBP52; FK506; ASSAY;
D O I
10.1021/ml1001272
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
There are strong indications for the involvement of cyclophilin 40 in diseases caused by misregulation of steroid hormone receptors, like prostate or breast cancer To identify novel inhibitors for this immunophilin, we developed a simplified fluorescence polarization assay based on the synthesis Of a fluorescein labeled tracer. This tracer was produced by a facile four-step synthesis involving Grubbs metathesis and standard amide bond coupling, to label cyclosporin A with fluorescein. We show the binding of this tracer to Cyp40 and Cyp18 with K-D values of 106 +/- 13 or 12 +/- 1 nM, respectively, by analyzing the anisotropy change and demonstrate its competition with cyclosporin A. Binding data obtained by fluorescence polarization were corroborated by an enzymatic activity assay. The described tracer allows for a robust assay in a high-throughput format to support the development of novel Cyp40 ligands.
引用
收藏
页码:536 / 539
页数:4
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