Multi-Pulse Fluorescence (MPF) is a new CFS core project, currently under development.
The basic idea of MPF is to perturb the sample with one light pulse and to start the time-resolved measurement at a delay time t with a second excitation pulse. The time-resolved data will be correlated with time-dependent structural changes in the protein following the perturbation pulse. This approach will be applied to proteins which undergo conformational changes in response to light, including hempglobin, rhodopsin and phytochromes. Both steady state and time-resolved measurements will be performed.
- Experimental arrangement for two-pulse
fluorescence measurements. L are lenses, P
are polarizers, D are diaphragms, R are
polarization rotators, and F are optical
filters. Long delay line DL1 is placed in the UV
and a fine delay line DL2 in the visible beam,
DF is a coated optical plate (dichroic filter) and
PD is a reference photodiode, used in time-