Fluorescence Resonance Energy Transfer (FRET) using peptides
Fluorescence resonance energy transfer (FRET) is a method that allows the distance-dependent interaction between the excited states of two distinct dye-linked molecules to be detected. The excitation is transferred from a donor to an acceptor without emitting a photon. The assay is rapid, highly sensitive, and straightforward to perform. Although it is possible to perform FRET using a single type of dye, the majority of applications require two.
FRET is used to measure the transfer of energy from the donor that is excited initially (dye 1) to an acceptor (dye 2). The wavelength at which a donor typically emits light, λd, generally overlaps with the absorption wavelength, λa, of the acceptor. The energy transfer occurs in one of two ways, depending on the chemical structure of the acceptor, if the donor and acceptor dyes are in close proximity (10–100?):
- a) If the acceptor is a dark quencher, the energy transferred energy could be converted into molecular vibrations
- b) If the acceptor is fluorescent, the transferred energy might be emitted as light with a longer wavelength
In this example, the donating (EDANS) and accepting groups (DABCYL) are attached to a natural substrate of HIV protease. In an uncleaved substrate, DABCYL quenches EDANS; therefore there is no detectable fluorescence. After the substrate has been cleaved by HIV-1 protease, DABCYL no longer quenches EDANS, allowing the EDANS fluorescence to be detected. Changes in the intensity of EDANS fluorescence can then be monitored to assess the efficiency of protease inhibitors.
FRET peptides can be used to study peptidase specificity because they allow reactions to be monitored continuously, allowing enzymatic activity to be determined rapidly. The peptide bonds between the donor/acceptor pair can be cleaved, which generates a fluorescent signal to allow nanomolar concentrations of enzyme activity to be measured. When intact, FRET peptides quench internal fluorescence; however, the cleavage of a peptide bond between the donor/acceptor pair releases a fluorescent signal that can be detected continuously, allowing enzyme activity to be quantified.
FRET peptides are used as suitable substrates in many different enzyme studies:
- Kinetic and functional characterization of peptidases, proteases, kinases, and phosphatases.
- Screening and detection of novel proteolytic enzymes.
- Conformational investigation of peptide folding.
Standard dye combinations used for FRET:
- Fluorescein and Dabcyl:FAM/Lys(DABCYL)
- Fluorescein and TAMRA: FAM/TAMRA
- Methoxy-coumarin-acetic-acid(MCA) and 2,4-Dinitrophenyl(DNP): MCA/Lys(Dnp).
- Ortho-aminobenzoic acid (Abz) and 2,4-dinitrophenyl (DNP) or N-(2,4-dinitrophenyl)ethylenediamine (EDDnp): ABZ/Tyr (NO2), ABZ/EDDnp
- DABCYL and Glu(EDANS)
Donor-acceptor pairs capable of quenching using resonance energy transfer in peptide substrates of proteolytic enzymes
|
Wavelengths (nm) |
Quencher |
Fluorophore |
Excitation |
Emission |
|
Dabcyl
Dansyl
DNP
Tyr (NO2) |
Edans
Trp
MCA
Abz |
336
336
328
320 |
490
350
393
420 |
The Forster Critical Distance for Common RET Donor-Acceptor Pairs
Donor |
Acceptor |
Forster Distance
(nm) |
|
Trp
Dansyl
Dansyl
Fluorescein
Cy3
|
Dansyl
FITC
Rhodamine
Tetramethylrhodamine
Cy5
|
2.1
3.3-4.1
4.3
4.9-5.5
>5.0
|
Reference:
An Angiotensin-(1-7) Endopeptidase in the Kidney Cortex, Proximal Tubules and Human HK-2 Epithelial Cells that is Distinct from Insulin Degrading Enzyme, American Journal of Physiology - Renal Physiology, 7 January 2015Vol. no. , DOI: 10.1152/ajprenal.00609.2014
Fluorescent peptide Angiotensin 1-7 (Ang-(1-7)) with FRET pair Abz/[Tyr7(NO2)] was synthesized by LifeTein. This FRET peptide was used to study the Ang-(1-7) endopeptidase in the renal renin angiotensin system. It was found that the endopeptidase is expressed within the renal proximal tubule. It may regulate Ang-(1-7) tone.
... 100 μM Abz-Ang-(1-7)- [Tyr7(NO2)],
an internally quenched fluorescent peptide (synthesized by LifeTein, South Plainfield, NJ, USA) for 20 hours or 0.5 nM 125I-(Ang-1-7) for 60 minutes at 37°C
...
FITC
Fluorescein isothiocyanate (FITC) is more reactive than carboxy ?uorescein, which must also be activated before use. FITC can react extensively with sulfhydryl groups， such as the side chains of reduced cysteine residues.
For many applications, ?uorescent labels can be introduced during chemical synthesis. After the selective unmasking of a protecting group, FITC might react with either lysine, an ornithine side chain, or with a primary amino group at the N-terminus of the growing peptide. In this latter case, an alkyl spacer such as aminohexanoic acid (Ahx) is introduced between the last amino acid and the thiourea linkage that is generated during the reaction between isothiocyanate and amine.
Under the acidic conditions required for linker cleavage, N-terminal FITC-labeled peptides undergo a cyclization step, which leads to the formation of ?uorescein with the subsequent removal of the last amino acid. This can be avoided when a spacer such as amino hexanoic acid is used, or if the targeted peptide is released from the resin via non-acidic cleavage.
Steric hindrance, which sometimes is the main reason for using Ahx, is no barrier to directly coupling FITC and the peptide. Ahx or b-Ala can be used successfully as spacers to generate FITC-labeled peptides.
An additional reactive fluorophore, tetramethylrhodamine (TAMRA), also exhibits properties that are not ideal for intracellular reactions. TAMRA-based probes result in the most uniform intracellular distribution of all common FRET probes and have the most efficient diffusion through the cytoplasm. Nevertheless, TAMRA chromophores offer multiple advantages compared with fluorescein. For example, TAMRA exhibits increased resistance to photobleaching than does fluorescein. Fluorescein is typically excited at 494 nm and emits fluorescence at 520 nm. In contrast, the maximum absorbance and emission of TAMRA occurs at 546 nm and 580 nm, respectively. Importantly, TAMRA contains one extra positive charge compared with, which might increase the interaction between TAMRA and target compounds, and also facilitate binding between the probe and the compound. Similar to Cy3, TAMRA is very stable and bright; therefore, it is an excellent flourochrome. Importantly, the combination of FITC and TAMRA can be used because of the separation between their respective excitation and emission maxima and because they do not quench each other.
Fluorescent dyes such as biotin and FITC can generally be added to either the N- or C-terminus of a peptide. Nevertheless, we recommend adding such modifications to the N terminus because it results in a shorter turnaround time, is more likely to be successful, and does not require additional coupling steps. Because peptides are synthesized from the C- to the N-terminus, the addition of an N-terminal modification is the final step in the SPPS protocol.
The majority of commonly used dyes are large aromatic compounds; therefore, the incorporation of these bulky molecules could prevent interactions between the peptide and the dye. This helps retention of the appropriate peptide conformation and biological activities. We also recommended that clients include a flexible spacer, such as the six-carbon linker Ahx, in their synthetic peptide projects because it increased the stability of the fluorescent label. FITC can also be linked readily to the thiol of a cysteine or to any amino group of lysine.
| Probe |
Ex (nm) |
Em (nm) |
MW |
Notes |
| Methoxycoumarin (MCA) |
360 |
410 |
317 |
Succinimidyl ester |
| Fluorescein (FITC) |
495 |
519 |
389 |
pH sensitive |
| X-Rhodamine |
570 |
576 |
548 |
|
| Rhodamine B |
570 |
590 |
|
|
Frequently Asked Questions: Peptide Synthesis
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Is a spacer required for fluorescent modification?
How should I dissolve peptides?
How do I choose the best level of peptide purity for my research?
Case Study 1
This case study shows the most commonly used approach for FRET assays. The fluorescent dye MCA (methoxycoumarine acetic acid) is incorporated at the N-terminus of a peptide, which was synthesized as a substrate for stromelysin, a matrix metalloprotease. The quencher N-3-(2, 4-dinitrophenyl)-L-2,3-diaminopropionyl (DPA) was then incorporated after the enzymatic hydrolysis of the scissile Gly-Leu peptide bond (Knight el al., 1992).
The sequence of the peptide used is as follows:
MCA-Pro-Leu-Gly-Leu-DPA-Ala-Arg-NH2
The peak absorbance and peak fluorescence of MCA occur at 328 nm and 393 nm, respectively. The DPA group exhibits strong absorption at 363 nm with a prominent shoulder at 410 nm. DPA can quench the fluorescence of MCA because this shoulder overlaps with the fluorescence peak of MCA.
A previous study demonstrated that a 1-μm solution of MCA-Pro-Leu (the product of enzymatic hydrolysis) showed excitation and emission at 328 nm and 393 nm, respectively, and was 130-fold more fluorescent than a comparable solution of MCA-Pro-Leu-Gly-Leu-DPA-Ala-Arg-NH2 (Knight el al., 1992).
Enzymatic hydrolysis of this peptide cause separation of the MCA and DPA groups and a large increase in MCA fluorescence. This increase in fluorescence can serve as an indicator of the speed of the reaction. This has allowed investigators to establish the values of Kcat/Km of this substrate for several members of the matrix metalloprotease family. This assay was recently used to determine the potency of potential inhibitors of stromelysin through measurement of the effects of the inhibitors on the initial velocity of the enzymatic reaction (Copeland et al., 1995)
Case Study 2
The client requested a very hydrophobic peptide 68 amino acid in length (85% purity) with FITC modification at the N-terminus. The peptide was successfully synthesized in 4 weeks.
HPLC Results:
MS Results:
