TY - JOUR
T1 - Design and characterization of a DNA-encoded, voltage-sensitive fluorescent protein
AU - Sakai, R.
AU - Repunte-Canonigo, V.
AU - Raj, Christopher D.
AU - Knöpfel, Thomas
N1 - Publisher Copyright:
© Federation of European Neuroscience Societies
PY - 2001/6
Y1 - 2001/6
N2 - Optical imaging of electrical activity has been suggested as a promising approach to investigate the multineuronal representation of information processing in brain tissue. While considerable progress has been made in the development of instrumentation suitable for high-speed imaging, intrinsic or extrinsic dye-mediated optical signals are often of limited use due to their slow response dynamics, low effective sensitivity, toxicity or undefined cellular origin. Protein-based and DNA-encoded voltage sensors could overcome these limitations. Here we report the design and generation of a voltage-sensitive fluorescent protein (VSFP) consisting of a voltage sensing domain of a potassium channel and a pair of cyan and yellow emitting mutants of green fluorescent protein (GFP). In response to a change in transmembrane voltage, the voltage sensor alters the amount of fluorescence resonance energy transfer (FRET) between the pair of GFP mutants. The optical signals respond in the millisecond time-scale of fast electrical signalling and are large enough to allow monitoring of voltage changes at the single cell level.
AB - Optical imaging of electrical activity has been suggested as a promising approach to investigate the multineuronal representation of information processing in brain tissue. While considerable progress has been made in the development of instrumentation suitable for high-speed imaging, intrinsic or extrinsic dye-mediated optical signals are often of limited use due to their slow response dynamics, low effective sensitivity, toxicity or undefined cellular origin. Protein-based and DNA-encoded voltage sensors could overcome these limitations. Here we report the design and generation of a voltage-sensitive fluorescent protein (VSFP) consisting of a voltage sensing domain of a potassium channel and a pair of cyan and yellow emitting mutants of green fluorescent protein (GFP). In response to a change in transmembrane voltage, the voltage sensor alters the amount of fluorescence resonance energy transfer (FRET) between the pair of GFP mutants. The optical signals respond in the millisecond time-scale of fast electrical signalling and are large enough to allow monitoring of voltage changes at the single cell level.
KW - Green fluorescent protein
KW - Membrane potential
KW - Microfluometry
KW - Potassium channel
UR - https://www.scopus.com/pages/publications/0034912282
UR - https://onlinelibrary.wiley.com/doi/10.1046/j.0953-816x.2001.01617.x
U2 - 10.1046/j.0953-816X.2001.01617.x
DO - 10.1046/j.0953-816X.2001.01617.x
M3 - Journal article
C2 - 11454036
AN - SCOPUS:0034912282
SN - 0953-816X
VL - 13
SP - 2314
EP - 2318
JO - European Journal of Neuroscience
JF - European Journal of Neuroscience
IS - 12
ER -