BRET is based on the energy derived from a luciferase reaction that can be used to excite a fluorescent protein if the latter is near the luciferase enzyme. The technology involves fusion of donor (luciferase) and acceptor (fluorescent) molecules to proteins of interest. Co-expression of fusion constructs in living cells enables their interaction to be studied in real time in a quantitative manner. Energy is transferred through nonradiative dipole–dipole coupling from the donor to the acceptor when in proximity (typically within 10 nm), resulting in fluorescence emission at a specific wavelength. The energy emitted by the acceptor relative to that emitted by the donor is termed the BRET signal. It is dependent upon the spectral properties, ratio, distance and relative orientation of the donor and acceptor molecules as well as the strength and stability of the interaction between the proteins of interest.
BRET is very similar tobut in FRET the donor is a fluorescent protein that has to be excited. As BRET does not require external light source to excite the donor it has very low background and does not suffer from issues often associated with FRET like autofluorescence, light scattering, or photobleaching. Other advantages of BRET are that it is a non-radioactive and homogeneous technology and that the ratio metric signal minimizes interferences from assay conditions.
Over the last years different BRET methods have been developed and all of them have their limitations and benefits. Various donor and acceptor pairs and their corresponding wavelengths can be found in the table below:
|Method||Donor||Substrate||Donor Emission [nm]||Acceptor||Acceptor Emission [nm]|
Coelenterazine 400a (Deep Blue C™)
Coelenterazine 400a (Deep Blue C™)
The original BRET method using Coelenterazine as substrate is nowadays called BRET 1 and is characterized by strong signals and long lifetime.
In comparison with BRET 1, BRET2 has a better separation between donor and acceptor emission peaks. This makes BRET 2 a better choice for assays where high signal to noise ratios are required. A clear limitation of BRET 2 is the low light emission and the short lifetime.
Enhanced BRET 2 (eBRET)
eBRET can have up to a 5-fold better signal as in the original BRET 2 version. eBRET uses a new Renilla luciferase mutant called Rluc8.
The Firefly luciferase in BRET 3 shows lower cellular autofluorescence at the emission wavelength (565 nm) but the disadvantages are weak signals and overlap between donor and acceptor emission peaks.
A brand-new BRET version is the Quantum Dot-BRET (QD-BRET). The emission peaks are clearly separated which makes QD-BRET ideal for screening applications. Disadvantages are the large size of the QD molecules (1.5 - 6 nm) and genetic coding of QD-proteins is not possible. QD proteins cannot be expressed in living cells and must be added.
NanoBRET™ uses a luciferase much brighter than conventional luciferases called NanoLuc®. There is very good separation between donor emission (460 nm) and acceptor emission (618 nm).
BRET can be measured in microplate readers to studyespecially in the field of G-protein coupled receptor research. The ability to study interactions in living mammalian cells circumvents many of the problems associated with techniques such as co-immunoprecipitation and yeast two-hybrid screening. The high sensitivity of BRET enables the study of proteins at physiological concentrations which is a significant advantage over techniques that require high levels of protein expression.
Especially in the field of G-protein coupled receptor research, BRET technology offers the opportunity to establish a homogeneous, universal and functional assay. Taking advantage of the fact that ß-arrestin which is naturally playing a role in the desensitization of the receptors; binds to the intracellular part of the activated receptor. G-protein coupled receptors are also referred to as 7-transmembrane (7TM) receptors and comprise the largest, most diverse superfamily of proteins known.
To get some idea of how important GPCRs are in drug discovery:
- Currently ~ 30 % of drugs are targeted against GPCRs
- Only 5 % of the known receptors are targeted with drugs
- To only 20 % of the rest the corresponding ligands are known
BRET publication compilation A compilation of scientific articles using Mithras or Tristar microplate readers for BRET.
PDF | 511.6 KB
NanoBRET™ with the TriStar² S Promega NanoBRET™ protein:protein interaction system with the TriStar² S Multimode Microplate Reader
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Comparison of filter sets for BRET1 using Mithras Comparison of filter sets for BRET1 assays: ß-arrestin2 (ßARR2) recruitment to the vasopressin V2 receptor using the Mithras LB 940 Multimode Microplate Reader
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Basic Considerations for BRET Assays with the Mithras Basic Considerations for Bioluminescence Resonance Energy Transfer (BRET) Assays for G-protein coupled receptor protein interactions in living cells
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BRET to monitor dynamic receptor-protein interactionswith the Mithras Bioluminescence Resonance Energy Transfer (BRET) as a means of monitoring dynamic receptor-protein interactions in living cells measured on LB 940 Mithras Multimode Microplate Reader
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BRET-based studies of receptor dynamics with Mithras Bioluminescence Resonance Energy Transfer (BRET)-based studies of receptor dynamics in living cells with Berthold’s Mithras Multimode Microplate Reader
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Aor capable of measuring luminescence with high-sensitivity using filters is the best combination for BRET; can also be used, but with reduced sensitivity. It is necessary to perform 2 measurements at different wavelengths, and hence a reader with at least 2 emission filters is required (this is not possible, for example, in readers using one single filter cube with 1 excitation filter + 1 emission filter). All microplate readers below are recommended for BRET.