Fluorescence correlation spectroscopy protein conformational studies

Applications of fluorescence correlation spectroscopy have included studies of sparse molecules on cell surfaces [264, 265], diffusion of Ugand-receptor complexes in cell membranes [266], conformational dynamics of DNA [150, 233], excited-state properties of flavins and flavoproteins [267], photodynamics of green- and red-fluorescent proteins [268,269], protein unfolding pathways [270] and lipid-protein interactions [271]. 

Fluorescence correlation spectroscopy (FCS) measures rates of diffusion, chemical reaction, and other dynamic processes of fluorescent molecules. These rates are deduced from measurements of fluorescence fluctuations that arise as molecules with specific fluorescence properties enter or leave an open sample volume by diffusion, by undergoing a chemical reaction, or by other transport or reaction processes. Studies of unfolded proteins benefit from the fact that FCS can provide information about rates of protein conformational change both by a direct readout from conformation-dependent fluorescence changes and by changes in diffusion coefficient. 

IV. Advantages and Disadvantages of Using Fluorescence Correlation Spectroscopy to Study Protein Conformational Changes... 

A number of macromolecular diffusion and conformational properties can be studied using fluorescence anisotropy, fluorescence correlation spectroscopy (ECS), and fluorescence recovery after photobleaching (FRAP). These techniques most commonly are applied to proteins labelled with highly fluorescent probes, but can exploit intrinsic fluorescence in some instances. In fluorescence anisotropy studies, polarized light is used to selectively excite molecules whose transition dipole moments are aligned with the electric field vector. Steady-state... 

The major reasons for using intrinsic fluorescence and phosphorescence to study conformation are that these spectroscopies are extremely sensitive, they provide many specific parameters to correlate with physical structure, and they cover a wide time range, from picoseconds to seconds, which allows the study of a variety of different processes. The time scale of tyrosine fluorescence extends from picoseconds to a few nanoseconds, which is a good time window to obtain information about rotational diffusion, intermolecular association reactions, and conformational relaxation in the presence and absence of cofactors and substrates. Moreover, the time dependence of the fluorescence intensity and anisotropy decay can be used to test predictions from molecular dynamics.(167) In using tyrosine to study the dynamics of protein structure, it is particularly important that we begin to understand the basis for the anisotropy decay of tyrosine in terms of the potential motions of the phenol ring.(221) For example, the frequency of flips about the C -C bond of tyrosine appears to cover a time range from milliseconds to nanoseconds.(222)... 

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