Fluorescence Cross Correlation Spectroscopy (FCCS) / Fluorescence Lifetime Cross Correlation Spectroscopy (FLCCS)

This employs the same principle as FCS except that the fluorescence signal from two different fluorescence species is measured in two separate channels simultaneously. A correlation analysis is performed between the intensity time trace from the two channels (as opposed to an auto-correlation analysis in the case of FCS). This will yield information on any correlated motion of the two-fluorescence species, such that if they are bound one observes a strong (cross-) correlation.

Unlike FLIM-FRET which may also be used to measure binding dynamics, there is no constraint on the relative orientations or distances between the two molecules (i.e. they may be separated by >10nm), not on there being any spectral overlap in the emission and absorption spectra of the two fluorescent species being studied.

 

Examples of use:

  • Binding (dynamics) or colocalization of two fluorescently-labelled molecules separated (especially by more >10nm).

 

Microscope used: Rig 1

 

Useful references:

 

Example from VBCF Advanced Microscopy facility:

  • coming soon

 

Expected Specs:

  • coming soon