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High-speed recording of neural spikes in awake mice and flies with a fluorescent voltage sensor.
Gong, Yiyang; Huang, Cheng; Li, Jin Zhong; Grewe, Benjamin F; Zhang, Yanping; Eismann, Stephan; Schnitzer, Mark J.
Afiliação
  • Gong Y; James H. Clark Center, Stanford University, Stanford, CA 94305, USA. CNC Program, Stanford University, Stanford, CA 94305, USA. Department of Biomedical Engineering, Duke University, Durham, NC 27708, USA. yiyang.gong@duke.edu mschnitz@stanford.edu.
  • Huang C; James H. Clark Center, Stanford University, Stanford, CA 94305, USA.
  • Li JZ; James H. Clark Center, Stanford University, Stanford, CA 94305, USA. CNC Program, Stanford University, Stanford, CA 94305, USA.
  • Grewe BF; James H. Clark Center, Stanford University, Stanford, CA 94305, USA. CNC Program, Stanford University, Stanford, CA 94305, USA.
  • Zhang Y; James H. Clark Center, Stanford University, Stanford, CA 94305, USA. CNC Program, Stanford University, Stanford, CA 94305, USA. Howard Hughes Medical Institute, Stanford University, Stanford, CA, USA.
  • Eismann S; James H. Clark Center, Stanford University, Stanford, CA 94305, USA. CNC Program, Stanford University, Stanford, CA 94305, USA.
  • Schnitzer MJ; James H. Clark Center, Stanford University, Stanford, CA 94305, USA. CNC Program, Stanford University, Stanford, CA 94305, USA. Howard Hughes Medical Institute, Stanford University, Stanford, CA, USA. yiyang.gong@duke.edu mschnitz@stanford.edu.
Science ; 350(6266): 1361-6, 2015 Dec 11.
Article em En | MEDLINE | ID: mdl-26586188
ABSTRACT
Genetically encoded voltage indicators (GEVIs) are a promising technology for fluorescence readout of millisecond-scale neuronal dynamics. Previous GEVIs had insufficient signaling speed and dynamic range to resolve action potentials in live animals. We coupled fast voltage-sensing domains from a rhodopsin protein to bright fluorophores through resonance energy transfer. The resulting GEVIs are sufficiently bright and fast to report neuronal action potentials and membrane voltage dynamics in awake mice and flies, resolving fast spike trains with 0.2-millisecond timing precision at spike detection error rates orders of magnitude better than previous GEVIs. In vivo imaging revealed sensory-evoked responses, including somatic spiking, dendritic dynamics, and intracellular voltage propagation. These results empower in vivo optical studies of neuronal electrophysiology and coding and motivate further advancements in high-speed microscopy.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Potenciais de Ação / Técnicas Biossensoriais / Transferência Ressonante de Energia de Fluorescência / Potenciais Somatossensoriais Evocados / Técnicas de Transferência de Energia por Ressonância de Bioluminescência / Neurônios Limite: Animals Idioma: En Revista: Science Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Potenciais de Ação / Técnicas Biossensoriais / Transferência Ressonante de Energia de Fluorescência / Potenciais Somatossensoriais Evocados / Técnicas de Transferência de Energia por Ressonância de Bioluminescência / Neurônios Limite: Animals Idioma: En Revista: Science Ano de publicação: 2015 Tipo de documento: Article