Author:
Crespo Emmanuel L.,Pal Akash,Prakash Mansi,Silvagnoli Alexander D.,Zaidi Zohair,Gomez-Ramirez Manuel,Tree Maya O.,Shaner Nathan C.,Lipscombe Diane,Moore Christopher,Hochgeschwender Ute
Abstract
AbstractWe developed a platform that utilizes a calcium-dependent luciferase to convert neuronal activity into activation of light sensing domains within the same cell. The platform is based on aGaussialuciferase variant with high light emission split by calmodulin-M13 sequences that depends on influx of calcium ions (Ca2+) for functional reconstitution. In the presence of its luciferin, coelenterazine (CTZ), Ca2+influx results in light emission that drives activation of photoreceptors, including optogenetic channels and LOV domains. Critical features of the converter luciferase are light emission low enough to not activate photoreceptors under baseline condition and high enough to activate photosensing elements in the presence of Ca2+and luciferin. We demonstrate performance of this activity-dependent sensor and integrator for changing membrane potential and driving transcription in individual and populations of neuronsin vitroandin vivo.
Publisher
Cold Spring Harbor Laboratory
Cited by
1 articles.
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