A Bright and Fast Red Fluorescent Protein Voltage Indicator That Reports Neuronal Activity in Organotypic Brain Slices

被引:113
作者
Abdelfattah, Ahmed S. [1 ]
Farhi, Samouil L. [2 ]
Zhao, Yongxin [1 ]
Brinks, Daan [2 ]
Zou, Peng [2 ]
Ruangkittisakul, Araya [3 ]
Platisa, Jelena [4 ,5 ]
Pieribone, Vincent A. [4 ,5 ,6 ]
Ballanyi, Klaus [3 ]
Cohen, Adam E. [2 ,7 ,8 ]
Campbell, Robert E. [1 ]
机构
[1] Univ Alberta, Dept Chem, 11227 Saskatchewan Dr, Edmonton, AB T6G 2G2, Canada
[2] Harvard Univ, Dept Chem & Chem Biol, Cambridge, MA 02138 USA
[3] Univ Alberta, Dept Physiol, Edmonton, AB T6G 2H7, Canada
[4] John B Pierce Fdn Lab Inc, New Haven, CT 06519 USA
[5] Yale Univ, Sch Med, Cellular & Mol Physiol, 333 Cedar St, New Haven, CT 06520 USA
[6] Yale Univ, Sch Med, Neurobiol, 333 Cedar St, New Haven, CT 06510 USA
[7] Harvard Univ, Dept Phys, Cambridge, MA 02138 USA
[8] Harvard Univ, Howard Hughes Med Inst, Cambridge, MA 02138 USA
基金
加拿大自然科学与工程研究理事会; 美国国家科学基金会; 加拿大健康研究院; 美国国家卫生研究院;
关键词
biosensors; fluorescence imaging; fluorescent proteins; genetically encoded indicators; protein engineering; voltage imaging; CALCIUM INDICATORS; ACTION-POTENTIALS; ESCHERICHIA-COLI; GREEN; PROBE; EXPRESSION; 2-PHOTON; SPIKING; CIRCUIT;
D O I
10.1523/JNEUROSCI.3484-15.2016
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Optical imaging of voltage indicators based on green fluorescent proteins (FPs) or archaerhodopsin has emerged as a powerful approach for detecting the activity of many individual neurons with high spatial and temporal resolution. Relative to green FP-based voltage indicators, a bright red-shifted FP-based voltage indicator has the intrinsic advantages of lower phototoxicity, lower autofluorescent background, and compatibility with blue-light-excitable channelrhodopsins. Here, we report a bright red fluorescent voltage indicator (fluorescent indicator for voltage imaging red; FlicR1) with properties that are comparable to the best available green indicators. To develop FlicR1, we used directed protein evolution and rational engineering to screen libraries of thousands of variants. FlicR1 faithfully reports single action potentials (similar to 3% Delta F/F) and tracks electrically driven voltage oscillations at 100 Hz in dissociated Sprague Dawley rat hippocampal neurons in single trial recordings. Furthermore, FlicR1 can be easily imaged with wide-field fluorescence microscopy. We demonstrate that FlicR1 can be used in conjunction with a blue-shifted channelrhodopsin for all-optical electrophysiology, although blue light photoactivation of the FlicR1 chromophore presents a challenge for applications that require spatially overlapping yellow and blue excitation.
引用
收藏
页码:2458 / 2472
页数:15
相关论文
共 53 条
[1]   Imaging neural circuit dynamics with a voltage-sensitive fluorescent protein [J].
Akemann, Walther ;
Mutoh, Hiroki ;
Perron, Amelie ;
Park, Yun Kyung ;
Iwamoto, Yuka ;
Knoepfel, Thomas .
JOURNAL OF NEUROPHYSIOLOGY, 2012, 108 (08) :2323-2337
[2]   Genetically encoded calcium indicators for multi-color neural activity imaging and combination with optogenetics [J].
Akerboom, Jasper ;
Calderon, Nicole Carreras ;
Tian, Lin ;
Wabnig, Sebastian ;
Prigge, Matthias ;
Tolo, Johan ;
Gordus, Andrew ;
Orger, Michael B. ;
Severi, Kristen E. ;
Macklin, John J. ;
Patel, Ronak ;
Pulver, Stefan R. ;
Wardill, Trevor J. ;
Fischer, Elisabeth ;
Schueler, Christina ;
Chen, Tsai-Wen ;
Sarkisyan, Karen S. ;
Marvin, Jonathan S. ;
Bargmann, Cornelia I. ;
Kim, Douglas S. ;
Kugler, Sebastian ;
Lagnado, Leon ;
Hegemann, Peter ;
Gottschalk, Alexander ;
Schreiter, Eric R. ;
Looger, Loren L. .
FRONTIERS IN MOLECULAR NEUROSCIENCE, 2013, 6
[3]   Optogenetic reporters [J].
Alford, Spencer C. ;
Wu, Jiahui ;
Zhao, Yongxin ;
Campbell, Robert E. ;
Knoepfel, Thomas .
BIOLOGY OF THE CELL, 2013, 105 (01) :14-29
[4]   A genetically targetable fluorescent probe of channel gating with rapid kinetics [J].
Ataka, K ;
Pieribone, VA .
BIOPHYSICAL JOURNAL, 2002, 82 (01) :509-516
[5]   Circular permutation and receptor insertion within green fluorescent proteins [J].
Baird, GS ;
Zacharias, DA ;
Tsien, RY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (20) :11241-11246
[6]  
Banker G., 1998, CULTURING NERVE CELL
[7]   A Fluorescent, Genetically-Encoded Voltage Probe Capable of Resolving Action Potentials [J].
Barnett, Lauren ;
Platisa, Jelena ;
Popovic, Marko ;
Pieribone, Vincent A. ;
Hughes, Thomas .
PLOS ONE, 2012, 7 (09)
[8]   Two-Photon Lifetime Imaging of Voltage Indicating Proteins as a Probe of Absolute Membrane Voltage [J].
Brinks, Daan ;
Klein, Aaron J. ;
Cohen, Adam E. .
BIOPHYSICAL JOURNAL, 2015, 109 (05) :914-921
[9]   RAPID CHANGES OF INTRACELLULAR FREE CALCIUM CONCENTRATION - DETECTION BY METALLOCHROMIC INDICATOR DYES IN SQUID GIANT-AXON [J].
BROWN, JE ;
COHEN, LB ;
DEWEER, P ;
PINTO, LH ;
ROSS, WN ;
SALZBERG, BM .
BIOPHYSICAL JOURNAL, 1975, 15 (11) :1155-1160
[10]  
Cai D, 2013, NAT METHODS, V10, P540, DOI [10.1038/NMETH.2450, 10.1038/nmeth.2450]