TY - JOUR
T1 - New photochemical tools for controlling neuronal activity
AU - Kramer, Richard H.
AU - Fortin, Doris L.
AU - Trauner, Dirk
N1 - Funding Information:
We thank the entire Kramer Lab for helpful discussions. This work was supported by grant EY018957 from the National Eye Institute (RHK), grant MH088484 from the National Institute of Mental Health (RHK), grant CHE0724214 from the National Science Foundation ((DT), and the Nanomedicine Development Center for the Optical Control of Biological Function (grant PN2EY018241 to RHK and DT).
PY - 2009/10
Y1 - 2009/10
N2 - Neurobiology has entered a new era in which optical methods are challenging electrophysiological techniques for their value in measuring and manipulating neuronal activity. This change is occurring largely because of the development of new photochemical tools, some synthesized by chemists and some provided by nature. This review is focused on the three types of photochemical tools for neuronal control that have emerged in recent years. Caged neurotransmitters, including caged glutamate, are synthetic molecules that enable highly localized activation of neurotransmitter receptors in response to light. Natural photosensitive proteins, including channelrhodopsin-2 and halorhodopsin, can be exogenously expressed in neurons and enable rapid photocontrol of action potential firing. Synthetic small molecule photoswitches can bestow light-sensitivity on native or exogenously expressed proteins, including K+ channels and glutamate receptors, allowing photocontrol of action potential firing and synaptic events. At a rapid pace, these tools are being improved and new tools are being introduced, thanks to molecular biology and synthetic chemistry. The three families of photochemical tools have different capabilities and uses, but they all share in enabling precise and noninvasive exploration of neural function with light.
AB - Neurobiology has entered a new era in which optical methods are challenging electrophysiological techniques for their value in measuring and manipulating neuronal activity. This change is occurring largely because of the development of new photochemical tools, some synthesized by chemists and some provided by nature. This review is focused on the three types of photochemical tools for neuronal control that have emerged in recent years. Caged neurotransmitters, including caged glutamate, are synthetic molecules that enable highly localized activation of neurotransmitter receptors in response to light. Natural photosensitive proteins, including channelrhodopsin-2 and halorhodopsin, can be exogenously expressed in neurons and enable rapid photocontrol of action potential firing. Synthetic small molecule photoswitches can bestow light-sensitivity on native or exogenously expressed proteins, including K+ channels and glutamate receptors, allowing photocontrol of action potential firing and synaptic events. At a rapid pace, these tools are being improved and new tools are being introduced, thanks to molecular biology and synthetic chemistry. The three families of photochemical tools have different capabilities and uses, but they all share in enabling precise and noninvasive exploration of neural function with light.
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U2 - 10.1016/j.conb.2009.09.004
DO - 10.1016/j.conb.2009.09.004
M3 - Review article
C2 - 19828309
AN - SCOPUS:70450207816
SN - 0959-4388
VL - 19
SP - 544
EP - 552
JO - Current Opinion in Neurobiology
JF - Current Opinion in Neurobiology
IS - 5
ER -