Engineering of a light-gated potassium channel

被引:102
作者
Cosentino, Cristian [1 ]
Alberio, Laura [1 ]
Gazzarrini, Sabrina [1 ]
Aquila, Marco [1 ]
Romano, Edoardo [1 ]
Cermenati, Solei [1 ]
Zuccolini, Paolo [1 ]
Petersen, Jan [2 ]
Beltrame, Monica [1 ]
Van Etten, James L. [3 ,4 ]
Christie, John M. [2 ]
Thiel, Gerhard [5 ]
Moroni, Anna [1 ]
机构
[1] Univ Milan, Dept Biosci, I-20122 Milan, Italy
[2] Univ Glasgow, Inst Mol Cell & Syst Biol, Glasgow G12 8QQ, Lanark, Scotland
[3] Univ Nebraska Lincoln, Dept Plant Pathol, Lincoln, NE 68583 USA
[4] Univ Nebraska Lincoln, Nebraska Ctr Virol, Lincoln, NE 68583 USA
[5] Tech Univ Darmstadt, Membrane Biophys, Darmstadt, Germany
基金
英国生物技术与生命科学研究理事会; 美国国家科学基金会;
关键词
CHLORIDE CHANNEL; ION CHANNELS; K+ CHANNEL; CHANNELRHODOPSIN; DOMAIN; LOV;
D O I
10.1126/science.aaa2787
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The present palette of opsin-based optogenetic tools lacks a light-gated potassium (K+) channel desirable for silencing of excitable cells. Here, we describe the construction of a blue-light-induced K+ channel 1 (BLINK1) engineered by fusing the plant LOV2-J alpha photosensory module to the small viral K+ channel Kcv. BLINK1 exhibits biophysical features of Kcv, including K+ selectivity and high single-channel conductance, but reversibly photoactivates in blue light. Opening of BLINK1 channels hyperpolarizes the cell to the K+ equilibrium potential. Ectopic expression of BLINK1 reversibly inhibits the escape response in light-exposed zebrafish larvae. BLINK1 therefore provides a single-component optogenetic tool that can establish prolonged, physiological hyperpolarization of cells at low light intensities.
引用
收藏
页码:707 / 710
页数:4
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