The role of dark states in the photodynamics of the green fluorescent protein examined with two-color fluorescence excitation spectroscopy

The green fluorescent protein (GFP) and its mutants are important fluoresce nt markers for the microscopy of biological specimens. Their photodynamics are governed by transitions between the neutral and anionic form of the lig ht emitting chromophore. We used two-color fluorescence excitation spectros copy to show that this is also true for mutants such as EGFP and E222Q, whi ch in their ground state do not show any absorption attributable to the neu tral chromophore. The photodynamics of E222Q are described within the frame work of a 4-level system comprising two dark states. Two-color fluorescence correlation spectroscopy (FCS) has been employed to determine the rate con stants for this system. The first of these states has a population rate of 3 x 10(5) s(-1) and a lifetime of 50 mu s, indicating that this is the trip let state. The second state, which we identified as the neutral chromophore , has a population rate of 4 x 10(5) s(-1) and a lifetime of 500 mu s Our d ata allude to the fact that, already at low intensities, a large fraction o f the molecules are in the dark states.