Journal of the American Chemical Society · 2009 · 103 citations · 17 references
Natural SciencesChemical BiologyMolecular BiologyBiomedical OpticsBiosensorsMolecular ImagingFluorescence ImagingFluorescence SpectroscopyMolecular Probe DevelopmentMolecular SensorsPhotophysics Of Fluorescent ProbesFluorescence BiosensingFluorescence ProbesFluorescent Chemical ProbesFluorescent ProbesMolecular Beacon ImagingNear-infrared Fluorescence ImagingSignal-to-background EnhancementSignal-to-background Ratio
Herein we demonstrate the use of a novel dimerization-based molecular beacon (MB) probe consisting of two metallo-phthalocyanine (Pc) fluorophores that use near-IR fluorescence, appropriate for highly specific and sensitive in vivo and/or in vitro DNA/RNA detection. Pc's possess a propensity to form nonfluorescent H-dimers that is utilized as the molecular "off" switch in the closed MB conformation. The "on" switch, which is generated when the solution target binds to the loop of the MB forming the open form, also provides two fluorophores for transduction resulting in a doubling of the extinction coefficient and improving the resulting fluorescence yield compared to a classical single-fluorophore/quencher MB system. In addition, the Pc-based MBs possess high thermal, photo, and chemical stabilities that are essential for many highly sensitive applications, such as molecular imaging. The dimer-based MBs were obtained using a simple single-step synthesis procedure and demonstrated excellent quenching efficiencies (98%) as well as a high signal-to-background ratio (approximately 60) exceeding the performance characteristics of many conventionally available MB probes.
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