Vaasa Angela, Viil Indrek, Enkvist Erki, Viht Kaido, Raidaru Gerda, Lavogina Darja, Uri Asko
Institute of Chemistry, University of Tartu, 2 Jakobi St., 51014 Tartu, Estonia.
Anal Biochem. 2009 Feb 1;385(1):85-93. doi: 10.1016/j.ab.2008.10.030. Epub 2008 Oct 31.
The bisubstrate fluorescent probe ARC-583 (Adc-Ahx-(D-Arg)(6)-d-Lys(5-TAMRA)-NH2) and its application for the characterization of both ATP- and protein/peptide substrate-competitive inhibitors of protein kinases PKA (cyclic AMP-dependent protein kinase) and ROCK (rho kinase) in fluorescence polarization-based assay are described. High affinity of the probe (K(D)=0.48 nM toward PKA) enables its application for the characterization of inhibitors with nanomolar and micromolar potency and determination of the active concentration of the kinase in individual experiments as well as in the high-throughput screening format. The probe can be used for the assessment of protein-protein interactions (e.g., between regulatory and catalytic subunits of PKA) and as a cyclic AMP biosensor.
描述了双底物荧光探针ARC-583(Adc-Ahx-(D-Arg)(6)-d-Lys(5-TAMRA)-NH2)及其在基于荧光偏振分析中用于表征蛋白激酶PKA(环磷酸腺苷依赖性蛋白激酶)和ROCK(rho激酶)的ATP和蛋白质/肽底物竞争性抑制剂的应用。该探针具有高亲和力(对PKA的K(D)=0.48 nM),使其能够用于表征具有纳摩尔和微摩尔效力的抑制剂,并在单个实验以及高通量筛选形式中测定激酶的活性浓度。该探针可用于评估蛋白质-蛋白质相互作用(例如,PKA的调节亚基和催化亚基之间的相互作用),并用作环磷酸腺苷生物传感器。