GEVIBench › All sensors › PROPS
PROPS
First microbial opsin-based voltage indicator, though only functional in bacteria and extremely dim.
- Category: Opsin GEVI
- Published: 2011-07-15 — Science 2011
- Response polarity: positive-going (fluorescence increases on depolarization)
- Spectrum: excitation peak 555 nm, emission peak 710 nm (PROPS)
- Plasmid: Addgene #33780
- Tags: NIR FP, Microbial, Bacteria-only
Headline values (as shown in the GEVIBench table)
| Metric | Value | Definition |
|---|---|---|
| Brightness (B/B_EGFP) | — | Molecular 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) | 4.7 / 4.7 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 | +150% | 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 mV | 0.8% (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) | 4 | Number of published research papers, tracked by GEVIBench, that used the sensor for an experiment (a popularity / track-record measure). |
Measurements and sources
Kinetics
- τ_on 4.7 ms, τ_off 4.7 ms at 25°C — Kralj 2011, Fig. 1D
ΔF/F per 100 mV
- +150%, 1P — Kralj 2011, Fig. 1C
Fluorescence–voltage (F–V) curve
ΔF/F (%) at each membrane potential, normalized to 0 at −70 mV: -150 mV: -47%; -130 mV: -41%; -110 mV: -29%; -90 mV: -13%; -70 mV: 0%; -50 mV: 19%; -30 mV: 42%; -10 mV: 55%; 10 mV: 75%; 30 mV: 91%; 50 mV: 100%; 70 mV: 112% — Kralj 2011, Fig. 1C
Research papers using PROPS (4)
- Electrical spiking in Escherichia coli probed with a fluorescent voltage-indicating protein — Kralj JM, Hochbaum DR, Douglass AD, Cohen AE, Science 2011 (E. coli (BW25113 and other strains), in vitro)
- Initial photophysical characterization of the proteorhodopsin optical proton sensor (PROPS) — Nadeau JL, Frontiers in Neuroscience 2015 (E. coli, in vitro)
- Voltage-gated calcium flux mediates Escherichia coli mechanosensation — Bruni GN, Weekley RA, Dodd BJT, Kralj JM, Proceedings of the National Academy of Sciences 2017 (E. coli, in vitro)
- Membrane voltage dysregulation driven by metabolic dysfunction underlies bactericidal activity of aminoglycosides — Bruni GN, Kralj JM, eLife 2020 (E. coli, in vitro)
Data and citation
- llms.txt — summary for language models
- llms-full.txt — every sensor in full (Markdown)
- gevis.json — all values and measurements with sources (JSON)
- gevis.csv — one row per sensor (CSV)
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.