Design and characterization of a DNA-encoded, voltage-sensitive fluorescent protein

  • R. Sakai
  • , V. Repunte-Canonigo
  • , Christopher D. Raj
  • , Thomas Knöpfel*
  • *Corresponding author for this work

Research output: Contribution to journalJournal articlepeer-review

199 Citations (Scopus)

Abstract

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.

Original languageEnglish
Pages (from-to)2314-2318
Number of pages5
JournalEuropean Journal of Neuroscience
Volume13
Issue number12
DOIs
Publication statusPublished - Jun 2001
Externally publishedYes

User-Defined Keywords

  • Green fluorescent protein
  • Membrane potential
  • Microfluometry
  • Potassium channel

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