Flash photolysis of caged IP3 to trigger intercellular Ca2+ waves
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Updated: Apr 16, 2026

Flash Photolysis of Caged Compounds in the Cilia of Olfactory Sensory Neurons
Published on: October 29, 2011
Elke Decrock1, Marijke De Bock1, Nan Wang1
1Department of Basic Medical Sciences, Physiology Group, Ghent University, 9000 Ghent, Belgium.
Abstract:
Caged IP3 is an inactive form of the second messenger IP3, consisting of the biologically active molecule linked to a cage group through a photolabile bond. This bond is cleaved by exposure to brief "flashes" of ultraviolet (UV) light, thereby releasing the active IP3 molecule. The protection of caged IP3 against metabolic transformation in combination with a defined time point of fast photoliberation of IP3 provides an efficient way to temporally and spatially control the cytosolic release of IP3 and subsequent increase of cytoplasmic Ca(2+). These properties make it an ideal method for kinetic studies and also a well-suited procedure to initiate intercellular Ca(2+) waves from a point source of IP3. This protocol describes cell loading with membrane impermeable caged IP3 and the UV flash illumination procedure.
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