Steady State and Time‐Dependent Fluorescent Peptide Assays for Protein Kinases

Abstract

AbstractProtein kinases catalyze the phosphorylation of proteins most commonly on Ser, Thr, and Tyr residues and regulate many cellular events in eukaryotic cells, such as cell cycle progression, transcription, metabolism, and apoptosis. Protein kinases each have a conserved ATP‐binding site and one or more substrate‐binding site(s) that exhibit recognition features for different protein substrates. By bringing ATP and a substrate into proximity, each protein kinase can transfer the γ phosphate of the ATP molecule to a hydroxyl group of the target residue on the substrate. In such a way, signaling pathways downstream from the substrate can be regulated based on the phosphorylated versus dephosphorylated status of the substrate. Although there are a number of ways to assay the activity of protein kinases, most of them are technically cumbersome and/or are indirect or based on quenched reactions. This protocol describes an assay employing a fluorescent peptide substrate to detect phosphorylation by protein kinases in real time. The assay is based on the principle that the phosphorylation of the peptide substrate leads to an increase in the fluorescence emission intensity of an appended fluorophore. We extend the application of this assay to an example of how to assess time‐dependent covalent inhibition of kinases as well. © 2024 Wiley Periodicals LLC.Basic Protocol 1: Measuring protein kinase activity using fluorescent peptidesAlternate Protocol: Measuring protein kinase activity using a fluorescence plate readerSupport Protocol: Labeling peptides with sox fluorophoreBasic Protocol 2: Measuring time‐dependent ATP‐competitive inhibition of protein kinases using fluorescent peptides