Table 1.
Method | Cellular resolution | Dynamics | False positives | False negatives | Applicability | Special features and characteristics |
---|---|---|---|---|---|---|
BiFC | ● | ○ | ● ● | ○ ● | ● ● | Suitable for weak/transient PPIs |
Split-Luc | ○ | ● | ● | ● | ● a | Dynamic assembly and disassembly of PPIs can be studied |
FRET-APB | ● | ● | ○ ● | ● | ● ● b | Fast data acquisition and analysis |
FRET-FLIM | ● ● | ● | ○ ● | ● | ○ ● c.d | High quality of acquired data |
BiFC and FRET | ● ● | ○ ● | ● ● | ● ● | ○ ● d,e | Analysis of trimeric complexes |
Triple FRET | ● ● | ○ ● | ○ ● | ● ● | ○ ● c,d,e | Analysis of trimeric complexes |
Homo-FRET | ● ● | ● ● | ○ ● | ● ● | ○ ● d | Analysis of higher order complexes Can be combined with FRET-FLIM |
FCCS | ○ ● | ● ● | ○ | ○ ● | ○d | Low concentration of POI needed Simultaneous detection of PPI and dynamics |
RICS and N&B | ○ ● | ● ● | ○ ● | ● | ● c | Simultaneous detection of PPI and dynamics |
KSP | ○ ● | ○ ● | ○ ● | ○ ● | ○ ● f | Analysis of higher order complexes. Inducible visualization of PPI. Can be added to other methods as intrinsic positive control |
‘○’ = ‘no or low’, ‘○ ●’ = ‘medium’, ‘●’ = ‘high’, ‘● ●’ = ‘very high’.
a Phosphorescence of chlorophyll can mask the signal of luciferase.
b Not suitable for moving proteins.
c Data acquisition and analysis can be time consuming.
d Special technical equipment might be needed,
e Appropriate controls needed.
f Rapamycin-induced effects must be considered.