High-throughput fluorescence polarization method for identification of FKBP12 ligands

被引:43
作者
Bollini, S
Herbst, JJ
Gaughan, GT
Verdoorn, TA
Ditta, J
Dubowchik, GM
Vinitsky, A
机构
[1] Bristol Myers Squibb Inc, Pharmaceut Res Inst, Dept Neurosci, Wallingford, CT USA
[2] Bristol Myers Squibb Inc, Pharmaceut Res Inst, Dept Lead Discovery, Wallingford, CT USA
[3] Bristol Myers Squibb Inc, Pharmaceut Res Inst, CNS Chem, Wallingford, CT USA
关键词
D O I
10.1177/1087057102238626
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
FKBP12 is best known as the target of the widely used immunosuppressive drug FK506 but may also play a role in neuronal survival. Noninummosuppressive ligands of FKBP12 have been shown to have neuroprotective and neuroregenerative activity both in vitro and in vivo, stimulating interest in the development of high-throughput screens to rapidly identify novel ligands. FKBP12 was expressed as a His(6)-fusion in bacteria and purified by metal ion affinity and gel filtration chromatography. A high-throughput fluorescence polarization assay was developed to identify novel ligands; of FKBP12. Dissociation constant values of known FKBP12 ligands measured by the new method agreed closely with K-i values obtained by assaying inhibition of the rotamase activity of the enzyme. The fluorescence polarization assay is rapid, robust, and inexpensive and does not generate radioactive waste. It is very well suited for high-throughput screening efforts.
引用
收藏
页码:526 / 530
页数:5
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