GEVIBench › All sensors › Archer2

Archer2

Archaerhodopsin variant that further suppresses photocurrents (~99× vs Arch WT, producing no peak current) at the expense of slower kinetics and lower sensitivity (60% ΔF/F per 100 mV) than its sibling Archer1 (~55×).

Headline values (as shown in the GEVIBench table)

MetricValueDefinition
Brightness (B/B_EGFP)0.0016× EGFPMolecular brightness relative to EGFP (extinction coefficient × quantum yield, or a measured ratio). Sensors not measured against EGFP directly are placed through a chain of pairwise brightness comparisons, combined by geometric mean.
Kinetics τ_on / τ_off (ms)—Activation / decay time constants in ms (amplitude-weighted mean τ for multi-exponential fits). The value shown averages the measurements made at physiological temperature (≥33 °C); if there are none, it is the measurement closest to 33 °C.
ΔF/F per 100 mV+60%Steady-state fluorescence change for a 100 mV depolarization step (−70 → +30 mV); the sign gives the polarity. The table shows the first listed measurement; the median across measurements (one-photon preferred) is used for sorting.
ΔF/F per mV0.45% (estimated from the F–V curve)Subthreshold sensitivity: fluorescence change per mV near rest (−90 to −50 mV). Where no value is reported directly, it is estimated from the F–V curve.
ΔF/F per AP—Fluorescence change per single action potential in neurons. The table shows the first listed measurement; the median across measurements (one-photon preferred) is used for sorting.
AP width (FWHM, ms)—Full width at half maximum of the optical spike waveform.
Photostability t75% @ 100 mW/mm²—Time for fluorescence to fall to 75% of its initial value under one-photon illumination, linearly dose-scaled to 100 mW/mm² (t50% is used where the 75% crossing falls inside a fast initial transient). Two-photon curves are not dose-scaled and are excluded.
Papers using it (N_used)3Number of published research papers, tracked by GEVIBench, that used the sensor for an experiment (a popularity / track-record measure).

Measurements and sources

ΔF/F per 100 mV

Brightness comparisons

Fluorescence–voltage (F–V) curve

ΔF/F (%) at each membrane potential, normalized to 0 at −70 mV: -100 mV: -15%; -80 mV: -4%; -70 mV: 0%; -60 mV: 5%; -50 mV: 11%; -40 mV: 18%; -20 mV: 30%; 0 mV: 42%; 20 mV: 54%; 30 mV: 58%; 50 mV: 70% — Flytzanis 2014, Fig. 1d

Research papers using Archer2 (3)

Data and citation

Cite GEVIBench as: Adam E. Cohen and Daozheng Gong (2026). Voltage imaging: A practical guide. Neuron. https://doi.org/10.1016/j.neuron.2026.08.002

Generated from the GEVIBench database on 2026-10-12.