Small molecule FP |
EOS |
Glutamate |
Glutamate binds of AMPA causes a fluorescence increase of small molecule dye; |
[40] |
|
PTMs |
H2O2
|
Based on the oxidation of boronate esters; |
[16,41] |
|
PFBS |
|
Based on C–S bond cleavage of perfluoro-benzyl sulfonates; |
[42] |
|
NBzF |
|
Based on oxidation-induced C–C bond cleavage of benzils; |
[43] |
|
SO3 H-APL |
|
Based on C–N bond cleavage of anilines; |
[44] |
|
DPPEA-HC |
|
Based on oxidation of phosphorous |
[45] |
|
ANRP |
CO |
Anchored to cell membrane and sense the CO by a metal palladium-catalysed reaction; |
[46] |
|
DAF |
NO |
Based on the reaction with NO to furnish fluorescent triazole derivatives; |
[47] |
Nanomaterial based FP |
C3N4 Nanoribbons |
Citrate |
Quenched by Cu2+ and then recovered by the addition of citrate; |
[48] |
Genetically encoded FP |
FICRhR |
cAMP |
Based on the dissociation of purified regulatory and catalytic subunits of PKA; |
[49–57] |
|
ICUE1 |
|
Form Epac1-cyan-YFP sandwich when it binds with cAMP; |
[58] |
|
cADDis |
|
cAMP binding of the regulatory region causes a large conformational change in EPAC 2; |
[59, 60] |
|
cdiA |
|
cdiA riboswitches fused with Spinach2 aptamer; |
[61] |
|
cGES |
cGMP |
cGMP binding domain from PDEs; |
[62, 63] |
|
cGi |
|
cGMP binding domains from PKG and from PDEs; |
[64] |
|
CGY |
|
cGMP binding of PKGs induced fluorescent change; |
[65] |
|
c-di-GMP-I |
c-di-GMP |
c-di-GMP riboswitches fused with Spinach aptamer |
[66–68] |
|
Bc RNA |
|
c-di-GMP riboswitches fused with two FP genes; |
[69] |
|
DNB sensor |
|
c-di-GMP binding aptamer fused into DNB, Broccoli as the; |
[70] |
|
Frex |
NADH |
NADH binds to Rex subunit causes the conformational change of cpFP; |
[71] |
|
Peredox |
[NAD+]/[NADH] |
The competition between NADH and NAD+ for binding to Rex subunit causes the conformational change of two FP; |
[72, 73] |
|
Rex YFP |
|
Different binding affinity of NAD+ and NADH to nucleotide-binding domains of each Rex subunit; |
[74] |
|
SoNar |
|
Binding of NAD+ or NADH to Rex subunit both induces changes in protein conformation and fluorescence; |
[75, 76] |
|
GluSnFR/FLIPE |
Glutamate |
Glutamate binds to GltI causes the conformational change of two FP; |
[77–82] |
|
FLIPQ-TV |
Glutamine |
Glutamate binds to GlnH causes the conformational change of two FP; |
[82] |
|
FLIP family |
Sugar |
Sugar binds to PBPs causes an increase in FRET between two FP; |
[83–89] |
|
roGFP/roGFP2 |
ROS |
ROS binds to the surface-exposed cysteine; |
[90] |
|
CY-RL5 |
Redox state |
Binds to redox linker 5 (RL5) causes an increase in FRET between two FP; |
[91] |
|
COSer |
CO |
CO binds to CO sensitive heme protein causes the conformational change of cpYFP; |
[92] |
|
sGC |
NO |
Combining endogenously expressed guanylate cyclase with a FRET-based cGMP indicator; |
[93] |
|
OGsor |
2OG |
Binds to 2OG-binding domain GAF causes an increase in FRET between two FP; |
[94] |
|
CIT |
Citrate |
Binds to citrate-binding domain CitA causes an increase in FRET between two FP; |
[95] |
|
Lactate sensor |
Lactate |
Binds to lactate-binding domain of bacterial transcription factor LldR causes an increase in FRET between two FP; |
[88] |
|
Lapronic |
Lactate/pyruvate |
Different binding affinity of lactate and pyruvate to the binding domains of transcriptional factor LutR subunit; |
[96] |