New photochemical tools for controlling neuronal activity

被引:126
作者
Kramer, Richard H. [1 ]
Fortin, Doris L. [1 ]
Trauner, Dirk [2 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[2] Univ Munich, Dept Chem, D-81377 Munich, Germany
基金
美国国家科学基金会;
关键词
ACETYLCHOLINE-RECEPTOR LIGAND; IN-VIVO CONTROL; GLUTAMATE RECEPTORS; ECTOPIC EXPRESSION; LIVING CELLS; PHOTORECEPTOR DEGENERATION; RETINAL DEGENERATION; 2-PHOTON PHOTOLYSIS; NEURAL CIRCUITRY; CAGED GLUTAMATE;
D O I
10.1016/j.conb.2009.09.004
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
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.
引用
收藏
页码:544 / 552
页数:9
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