TABLE 1.
Key characteristics of red fluorescent proteins with excitation peak at 580–590 nm.
| Crimson | mCherry | mKate2 | FusionRed | |
|---|---|---|---|---|
| Ex peak (nm) | 588 | 587 | 588 | 580 |
| Em peak (nm) | 617 | 610 | 633 | 608 |
| EC (mM−1cm−1) | 77 | 72 | 63 | 95 |
| QY | 0.42 | 0.22 | 0.4 | 0.19 |
| Brightness a | 32 | 16 | 25 | 18 |
| Photostability (s) b | 49 | 68 | 58 | 131 |
| Maturation half-time (min) c | 14 | 15 | < 20 | 130 |
| Maturation efficiency d | 50% | 44% | 49% | 24% |
| pKa | 4.2 | < 4.5 | 5.4 | 4.6 |
| Oligomerization | dimer | monomer | dimer | monomer |
Calculated as the product of QY at peak excitation and EC in units of mM−1 cm−1.
Predicted time for fluorescence to photobleach by 50% under arc-lamp illumination with excitation intensity adjusted to produce 1,000 emission photons per molecule per second.
Time for fluorescence to obtain half-maximal value after exposure to oxygen.
Functional chromophore concentration divided by total protein concentration. Functional chromophore is determined using the base-denaturation method as EC measurement. This excludes unfolded and broken-chromophore (backbone cleavage before the first residue of chromophore) components. Total protein is determined by absorbance at 280 nm.