Development of luminescent probes for real‐time detection of the CDK/PP2A balance during the cell cycle.

From a biochemical viewpoint, the cell cycle is controlled by the phosphorylation of cyclin‐dependent kinase (CDK) substrates, and the phosphorylation level is determined by the enzymatic balance between CDK and protein phosphatase 2A (PP2A). However, the conventional techniques for analyzing protein phosphorylation using radioisotopes and antibodies involve many operational steps and take days before obtaining results, making them difficult to apply to high‐throughput screening and real‐time observations. In this study, we developed luminescent probes with a light intensity that changes depending on its phosphorylation state. We modified the Nano‐lantern probe (Renilla luciferase‐based Ca2+ probe) by introducing a CDK‐substrate peptide and a phosphopeptide‐binding domain into the luciferase. Our initial trial resulted in new probes that could report the CDK/PP2A balance in a purified system. Further modifications of these probes (replacing the phospho‐Ser with phospho‐Thr and randomly replacing its surrounding amino acids) improved the dynamic range by up to four‐fold, making them practical for use in the Xenopus egg extracts system, where many physiological events can be reproduced. Taken together, our new probes enabled the monitoring of the CDK/PP2A balance in real time, and are applicable to high‐throughput systems; the new probes thus appear promising for use in substrate and drug screening. [ABSTRACT FROM AUTHOR]