Abstract

Bioluminescence resonance energy transfer (BRET) is the non-radiative transfer of energy from a bioluminescent protein donor to a fluorophore acceptor. It shares all the formalism of Förster resonance energy transfer (FRET) but differs in one key aspect: that the excited donor here is produced by biochemical means and not by an external illumination. Often the choice of BRET source is the bioluminescent protein Renilla luciferase, which catalyzes the oxidation of a substrate, typically coelenterazine, producing an oxidized product in its electronic excited state that, in turn, couples with a proximal fluorophore resulting in a fluorescence emission from the acceptor. The acceptors pertinent to this discussion are semiconductor quantum dots (QDs), which offer some unrivalled photophysical properties. Amongst other advantages, the QD’s large Stokes shift is particularly advantageous as it allows easy and accurate deconstruction of acceptor signal, which is difficult to attain using organic dyes or fluorescent proteins. QD-BRET systems are gaining popularity in non-invasive bioimaging and as probes for biosensing as they don’t require external optical illumination, which dramatically improves the signal-to-noise ratio by avoiding background auto-fluorescence. Despite the additional advantages such systems offer, there are challenges lying ahead that need to be addressed before they are utilized for translational types of research.

Highlights

  • The ‘cold’ flashing light of fireflies has fascinated and intrigued people for centuries

  • Newly introduced NanoLuc is another mutant luciferase that has less frequently been fused with quantum dots (QDs)

  • The examples described above clearly imply the potential of QD–Luc system as a powerful imaging tool, the same may be true for their employment as a sensing probe

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Summary

Introduction

The ‘cold’ flashing light of fireflies has fascinated and intrigued people for centuries. They are qualified as an acceptor only when the associated donor has a comparable radiative lifetime, which is observed in lanthanide phosphorescence or processes like bio or chemiluminescence but not among most of the available conventional organic fluorophore dyes [14,15,16,17]. Their broad absorption spectra allow them to be excited at a wavelength far away from the discrete PL, contributing to their large effective Stokes shift.

System Design and Ligation Strategy
Schematic
Images
Biosensing
Application
Therapeutics
Anisotropic-QD–FLuc Constructs
BRET-Multistep FRET Constructs
Conclusions and Outlook
Full Text
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