4.5 Article

High-affinity bisubstrate probe for fluorescence anisotropy binding/displacement assays with protein kinases PKA and ROCK

Journal

ANALYTICAL BIOCHEMISTRY
Volume 385, Issue 1, Pages 85-93

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ab.2008.10.030

Keywords

FP assay; Fluorescence anisotropy; cAMP-dependent protein kinase (PKA); Rho kinase (ROCK); Bisubstrate inhibitor; Biosensor

Funding

  1. Estonian Science Foundation [6710]
  2. Estonian Ministry of Education and Sciences [SF0180121s08]

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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. (C) 2008 Elsevier Inc. All rights reserved.

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