Table I.
Timea | Tryptophanb |
Green chromophorec |
|||||
---|---|---|---|---|---|---|---|
λmax (nm) | Parameter Ad | 〈τ〉e (ns) | λmax (nm) | Imax | 〈τ〉f (ns) | ||
EGFP | 1,2 | 336 | 1.49 | 4.0 ± 0.2 | 512 | 1 | 2.6 ± 0.3 |
EGFP/Arg96Cys | 1,2 | 340 | 1.18 | 4.2 ± 0.2 | 512 | 0.2 | 2.5 ± 0.3 |
EGFP/Arg96Ser | 1 | 324 | 2.07 | –– | –– | –– | |
2 | 323 | 2.08 | 2.7 ± 0.3 | 500 | 0.02 | 1.8 ± 0.4 | |
EGFP/Arg96Ala | 1 | 323 | 2.34 | –– | –– | –– | |
2 | 320 | 2.52 | 2.2 ± 0.3 | 502 | 0.02 | 2.8 ± 0.4 |
In column “time” 1 indicates that experiment was performed just after purification, 2 indicates that experiment was performed after samples incubation for one year.
Tryptophan fluorescence was excited at 297 nm.
Green chromophore fluorescence was excited at 365 nm.
A = (I320/I365)297, where I320 and I365 are fluorescence intensities at λem 320 and 365 nm, respectively, and λex 297 nm.
The lifetime of tryptophan fluorescence decay was determined upon fluorescence recording at 340 nm.
The lifetime of green chromophore fluorescence decay was determined upon recording fluorescence at wavelength corresponding to maximum of emission spectrum.