Journal Article

Mechanistic Studies of the Genetically Encoded Fluorescent Protein Voltage Probe ArcLight

Cohen, Lawrence B., Pieribone, Vincent A., Chen, Fuyi, Loturco, Joseph J., Bondar, Alexey, Lazar, Josef, Jin, Lei, Han, Zhou

2014

Overview

ArcLight, a genetically encoded fluorescent protein voltage probe with a large ΔF/ΔV, is a fusion between the voltage sensing domain of the Ciona instestinalis voltage sensitive phosphatase and super ecliptic pHluorin carrying a single mutation (A227D in the fluorescent protein). Without this mutation the probe produces only a very small change in fluorescence in response to voltage deflections (∼ 1%). The large signal afforded by this mutation allows optical detection of action potentials and sub-threshold electrical events in single-trials in vitro and in vivo. However, it is unclear how this single mutation produces a probe with such a large modulation of its fluorescence output with changes in membrane potential. In this study, we identified which residues in super ecliptic pHluorin (vs eGFP) are critical for the ArcLight response, as a similarly constructed probe based on eGFP also exhibits large response amplitude if it carries these critical residues. We found that D147 is responsible for determining the pH sensitivity of the fluorescent protein used in these probes but by itself does not result in a voltage probe with a large signal. We also provide evidence that the voltage dependent signal of ArcLight is not simply sensing environmental pH changes. A two-photon polarization microscopy study showed that ArcLight's response to changes in membrane potential includes a reorientation of the super ecliptic pHluorin. We also explored different changes including modification of linker length, deletion of non-essential amino acids in the super ecliptic pHluorin, adding a farnesylation site, using tandem fluorescent proteins and other pH sensitive fluorescent proteins.

• Publisher: Public Library of Science,Public Library of Science (PLoS)
• Subject: Action Potentials / Amino acids / Amino Acids - chemistry / Amino Acids - genetics / Amino Acids - metabolism / Animals / Biology and Life Sciences / Cells, Cultured / Ciona / Coding / Ecliptic / Electric potential / Environmental changes / Fluorescence / Fluorescent Dyes - chemistry / Fluorescent Dyes - metabolism / Fluorescent indicators / Genetic code / Green Fluorescent Proteins - chemistry / Green Fluorescent Proteins - genetics / Green Fluorescent Proteins - metabolism / HEK293 Cells / Humans / Hydrogen ions / Hydrogen-Ion Concentration / Investigations / John B / Kinetics / Laboratories / Localization / Luminescent Proteins - chemistry / Luminescent Proteins - genetics / Luminescent Proteins - metabolism / Mammals / Medicine / Membrane potential / Membrane Potentials / Microscopy / Microscopy, Confocal / Molecular biology / Mutation / Mutation, Missense / Neurobiology / Neurons - metabolism / Neurons - physiology / Neurosciences / Patch-Clamp Techniques / pH effects / Phosphatase / Physiology / Prenylation / Proteins / Rats / Recombinant Fusion Proteins - chemistry / Recombinant Fusion Proteins - genetics / Recombinant Fusion Proteins - metabolism / Residues / Science / Sensors / Spectrometry, Fluorescence / Voltage