Table 1.
Applications | FPs | Affinity Tag | SNAP-Tag | Notes |
---|---|---|---|---|
In vivo imaging | + a | + | ||
Substrate utilization | + | − | − | FPs do not need of any substrate for their fluorescence |
Emission spectra | ± | − | + | FPs are in a limited number with respect to chemical probes |
Time-resolved fluorescence | ± | − | + | |
Multi-colour fluorescence | ± | − | + | For FPs, multi-cloning and expression is necessary |
In vitro applications | ± | ± | + | |
Variety of chemical group labelling | − | − | + | |
Pulse-chase analysis | − | − | + | Fresh synthetized FPs cannot be efficiently quenched |
Anaerobic conditions | − | + | + | FPs’ fluorophore formation requires oxygen |
Protein purification | + | + | + | Utilization of the GFP-trap matrix |
Protein immobilization | + | + | + | Utilization of the GFP-trap matrix |
Pull-down experiments | + | + | + | Utilization of the GFP-trap matrix |
a +, fully applicable or advantageous; ±, limited applicability; -, not applicable or disadvantageous; FPs = fluorescent proteins.