TY - JOUR
T1 - Photochemical activation of TRPA1 channels in neurons and animals
AU - Kokel, David
AU - Cheung, Chung Yan J.
AU - Mills, Robert
AU - Coutinho-Budd, Jaeda
AU - Huang, Liyi
AU - Setola, Vincent
AU - Sprague, Jared
AU - Jin, Shan
AU - Jin, Youngnam N.
AU - Huang, Xi Ping
AU - Bruni, Giancarlo
AU - Woolf, Clifford J.
AU - Roth, Bryan L.
AU - Hamblin, Michael R.
AU - Zylka, Mark J.
AU - Milan, David J.
AU - Peterson, Randall T.
PY - 2013/4
Y1 - 2013/4
N2 - Optogenetics is a powerful research tool because it enables high-resolution optical control of neuronal activity. However, current optogenetic approaches are limited to transgenic systems expressing microbial opsins and other exogenous photoreceptors. Here, we identify optovin, a small molecule that enables repeated photoactivation of motor behaviors in wild-type zebrafish and mice. To our surprise, optovin's behavioral effects are not visually mediated. Rather, photodetection is performed by sensory neurons expressing the cation channel TRPA1. TRPA1 is both necessary and sufficient for the optovin response. Optovin activates human TRPA1 via structure-dependent photochemical reactions with redox-sensitive cysteine residues. In animals with severed spinal cords, optovin treatment enables control of motor activity in the paralyzed extremities by localized illumination. These studies identify a light-based strategy for controlling endogenous TRPA1 receptors in vivo, with potential clinical and research applications in nontransgenic animals, including humans.
AB - Optogenetics is a powerful research tool because it enables high-resolution optical control of neuronal activity. However, current optogenetic approaches are limited to transgenic systems expressing microbial opsins and other exogenous photoreceptors. Here, we identify optovin, a small molecule that enables repeated photoactivation of motor behaviors in wild-type zebrafish and mice. To our surprise, optovin's behavioral effects are not visually mediated. Rather, photodetection is performed by sensory neurons expressing the cation channel TRPA1. TRPA1 is both necessary and sufficient for the optovin response. Optovin activates human TRPA1 via structure-dependent photochemical reactions with redox-sensitive cysteine residues. In animals with severed spinal cords, optovin treatment enables control of motor activity in the paralyzed extremities by localized illumination. These studies identify a light-based strategy for controlling endogenous TRPA1 receptors in vivo, with potential clinical and research applications in nontransgenic animals, including humans.
UR - http://www.scopus.com/inward/record.url?scp=84875457497&partnerID=8YFLogxK
U2 - 10.1038/nchembio.1183
DO - 10.1038/nchembio.1183
M3 - Article
C2 - 23396078
AN - SCOPUS:84875457497
SN - 1552-4450
VL - 9
SP - 257
EP - 263
JO - Nature Chemical Biology
JF - Nature Chemical Biology
IS - 4
ER -