Light-gated integrator for highlighting kinase activity in living cells

Protein kinases are key signaling nodes that regulate fundamental biological and disease processes. Illuminating kinase signaling from multiple angles can provide deeper insights into disease mechanisms and improve therapeutic targeting. While fluorescent biosensors are powerful tools for visualizin...

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Veröffentlicht in:Nature communications 2024-09, Vol.15 (1), p.7804-13, Article 7804
Hauptverfasser: Lin, Wei, Phatarphekar, Abhishek, Zhong, Yanghao, Liu, Longwei, Kwon, Hyung-Bae, Gerwick, William H., Wang, Yingxiao, Mehta, Sohum, Zhang, Jin
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Sprache:eng
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Zusammenfassung:Protein kinases are key signaling nodes that regulate fundamental biological and disease processes. Illuminating kinase signaling from multiple angles can provide deeper insights into disease mechanisms and improve therapeutic targeting. While fluorescent biosensors are powerful tools for visualizing live-cell kinase activity dynamics in real time, new molecular tools are needed that enable recording of transient signaling activities for post hoc analysis and targeted manipulation. Here, we develop a light-gated kinase activity coupled transcriptional integrator (KINACT) that converts dynamic kinase signals into “permanent” fluorescent marks. KINACT enables robust monitoring of kinase activity across scales, accurately recording subcellular PKA activity, highlighting PKA activity distribution in 3D cultures, and identifying PKA activators and inhibitors in high-throughput screens. We further leverage the ability of KINACT to drive signaling effector expression to allow feedback manipulation of the balance of Gα s R201C -induced PKA and ERK activation and dissect the mechanisms of oncogenic G protein signaling. Real-time biosensors have been developed for visualizing kinase activity dynamics, but they are confronted with many challenges. Here, the authors develop a light-gated KINACT integrator for post hoc analysis of transient kinase activity and signalling manipulation.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-024-51270-4