Spectral properties of PhoCl variantsa.
Protein | Extinction coefficientsb,c (mM−1 cm−1) | Quantum yieldb 488 nm | Brightness 488 nm (mM−1 cm−1) | Dissociation half times (s) | Dissociation efficiencyd (%) | Reference | |
---|---|---|---|---|---|---|---|
ε (488 nm) | ε (405 nm) | ||||||
mMaple | 22 ± 0 | 11 ± 2 | 0.89 | 20 | NA | NA | 34 |
PhoCl1 | 34 ± 0 | 8.9 ± 0.8 | 0.73 | 25 | 570 | 71 | 5 |
PhoCl2c | 24 ± 3 | 11 ± 1 | 0.48 | 12 | 700 | 92 | This work |
PhoCl2f | 26 ± 2 | 12 ± 1 | 0.50 | 13 | 76 | 88 | This work |
PhoCl1.5f-MV | 30 ± 4 | 12 ± 2 | 0.53 | 16 | 130 | 90 | This work |
PhoCl1.5f-L | 26 ± 2 | 12 ± 0 | 0.45 | 12 | 140 | 79 | This work |
PhoCl1.5f-MVS | 25 ± 0 | 13 ± 0 | 0.29 | 7.3 | 30 | 93 | This work |
PhoCl1.5f-LS | 22 ± 3 | 13 ± 3 | 0.36 | 7.9 | 21 | 85 | This work |
PhoCl1.5f-MVLS | NA | NA | NA | NA | 14 | NA | This work |
All measurement were performed with purified proteins in PBS solution (pH 7.4).
EGFP extinction coefficient of 56 mM−1 cm−1 (ref. 36) and quantum yield of 0.6 (ref. 37) at 488 nm were used as reference standards.
Mean ± SD for each protein was determined via alkali denaturation method from two independent protein preparations.
Dissociation efficiencies listed in this table were characterized by gel filtration chromatography (GFC) assay.