GEVIBench › All sensors › HVI+
HVI+
Positive-going variant of chemigenetic voltage indicator HVI.
- Category: Chemigenetic GEVI
- Published: 2025-08-08 — Science Advances 2025
- Derived from: HVI
- Response polarity: positive-going (fluorescence increases on depolarization)
- Spectrum: excitation peak 556 nm, emission peak 571 nm (HVI+ (Cy3b))
- Tags: Ace opsin, Cy3b, Positive-going
Headline values (as shown in the GEVIBench table)
| Metric | Value | Definition |
|---|---|---|
| Brightness (B/B_EGFP) | 1.11× 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) | 6.8 / 5.5 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 | +55% | 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 | 0.22% | 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 | 22.3% | 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) | 9.5 ms | Full width at half maximum of the optical spike waveform. |
| Photostability t75% @ 100 mW/mm² | 3.2 min | 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) | 1 | 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 6.77 ms, τ_off 5.48 ms at 25°C — Liu 2025, Table S2
ΔF/F per 100 mV
- +55%, 1P, dye Cy3b — Liu 2025, Fig. 2E
ΔF/F per mV (subthreshold)
- 0.22%/mV — Liu 2025, Fig. 2G
ΔF/F per action potential
- 22.3%, 1P, dye Cy3b — Liu 2025, Fig. 2C
AP width (FWHM)
- 5 ms at 1000 Hz sampling, Rat, cultured hippocampal neurons, in vitro, 1P, 25°C — Liu 2025, Fig. 3B
- 14 ms at 200 Hz sampling, Mouse, pancreatic islet β cells, ex vivo, 1P, 37°C — Liu 2025, Fig. 6F
Brightness comparisons
- 0.53× the brightness of HVI — Liu 2025, Fig. S5C
Photobleaching
- t75% = 381 s at 50 mW/mm², 1P — Liu 2025, Fig. S7
Fluorescence–voltage (F–V) curve
ΔF/F (%) at each membrane potential, normalized to 0 at −70 mV: -100 mV: -10%; -80 mV: -5%; -70 mV: 0%; -60 mV: 6%; -40 mV: 15%; -20 mV: 25%; 0 mV: 37%; 20 mV: 47%; 40 mV: 57%; 60 mV: 67%; 80 mV: 78%; 100 mV: 88% — Liu 2025, Fig. 2E
Research papers using HVI+ (1)
- Positive-going hybrid indicators for voltage imaging in excitable cells and tissues — Liu S, et al., Science Advances 2025 (Rat, hippocampal neurons, in vitro; rat, cardiomyocytes, in vitro; mouse, pancreatic islets, ex vivo)
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.