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Updated: Jan 20, 2026
cAMP-dependent Protein Kinase Pathways
Efficient photocaging of a tight-binding bisubstrate inhibitor of cAMP-dependent protein kinase
Tanel Sõrmus1, Darja Lavogina1, Erki Enkvist1
1Institute of Chemistry, University of Tartu, 14A Ravila St., 50411 Tartu, Estonia. kaido.viht@ut.ee.
Abstract:
Photocaging of a tight-binding bisubstrate inhibitor of cAMP-dependent protein kinase (PKA) with a nitrodibenzofuran-based group fully abolished its inhibitory potency. The affinity difference between the photocaged and the active inhibitor was over 5 orders of magnitude. The photocaged inhibitor disrupted the PKA holoenzyme in cell lysates upon photolysis under a 398 nm LED.
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