The principle of fluorescence correlation spectroscopy is outlined. The tec
hnique has been applied to a mutant of the well-known green fluorescent pro
tein. A comparative study has been made with time-resolved fluorescence ani
sotropy. The latter experiment shows that the fluorophore is rigidly bound
inside the protein matrix follows the rotation of the whole protein and doe
s not show any fast restricted motion. It is evident from fluorescence corr
elation spectroscopy that some excited state reaction plays a role, since t
he autocorrelation traces show a significant effect on the incident laser p
ower. Other potential applications of fluorescence correlation spectroscopy
are presented as taken from very recent publications.