A Photoactivatable Botulinum Neurotoxin for Inducible Control of Neurotransmission

Regulated secretion is critical for diverse biological processes ranging from immune and endocrine signaling to synaptic transmission. Botulinum and tetanus neurotoxins, which specifically proteolyze vesicle fusion proteins involved in regulated secretion, have been widely used as experimental tools to block these processes. Genetic expression of these toxins in the nervous system has been a powerful approach for disrupting neurotransmitter release within defined circuitry, but their current utility in the brain and elsewhere remains limited by lack of spatial and temporal control. Here we engineered botulinum neurotoxin B so that it can be activated with blue light. We demonstrate the utility of this approach for inducibly disrupting excitatory neurotransmission, providing a first-in-class optogenetic tool for persistent, light-triggered synaptic inhibition. In addition to blocking neurotransmitter release, this approach will have broad utility for conditionally disrupting regulated secretion of diverse bioactive molecules, including neuropeptides, neuromodulators, hormones, and immune molecules. [Display omitted] •Few tools allow inhibition of neural activity for long time periods with light•We engineered botulinum neurotoxin B so that it can be activated with blue light•Photoactivated botulinum toxin efficiently cleaves the SNARE protein VAMP2•We demonstrate utility in diverse systems, from mammalian brain slices to worms Few tools in neuroscience allow long-term synapse inhibition with light. We engineered botulinum neurotoxin B so that it can be switched on with blue light. Light activation results in robust proteolysis of VAMP2, a SNARE protein universally required for neurotransmitter release.