A long-wavelength quantum dot-concentric FRET configuration: characterization and application in a multiplexed hybridization assay. Issue 12 (6th April 2016)

• Record Type: Journal Article
• Authors: Li, Jia Jun; Algar, W. Russ
• Is Part Of: Analyst. Volume 141:Issue 12(2016)
• Page Start: 3636
• Page End: 3647
• Publication Date: 2016-04-06
• Subjects: Chemistry, Analytic -- Periodicals; 543
• DOI: 10.1039/c6an00492j
• Languages: English
• ISSNs: 0003-2654

Abstract

Abstract : Quantum dot-based concentric Förster resonance energy transfer (cFRET) is a promising modality for the development of multifunctional fluorescent probes for bioanalysis and bioimaging. A new long-wavelength configuration and multiplexed hybridization assay format expands the scope of cFRET. Abstract : Quantum dot-based concentric Förster resonance energy transfer (cFRET) is a promising modality for the development of multifunctional fluorescent probes for bioanalysis and bioimaging. To date, the scope of cFRET has been largely limited to a prototypical configuration with a particular combination of quantum dot (QD) and fluorescent dyes linked through peptides. Expansion of the scope of cFRET is critical for its further development. Here, we expand the scope of cFRET in two capacities. First, we design and characterize a new long-wavelength cFRET configuration that combines red- and deep-red fluorescent dyes, Alexa Fluor 633 and Alexa Fluor 680, with an orange-emitting QD. Sequential and competitive energy transfer pathways are characterized through a rate analysis, where the balance of these rates more strongly favours competitive energy transfer in the new long-wavelength configuration versus sequential energy transfer in the previous prototypical configuration. Although the new cFRET configuration is more susceptible to photobleaching, its superior brightness and longer-wavelength excitation and emission provide an order of magnitude higher signal-to-background ratios in biological matrices ( e.g., serum, blood) than the previous prototypical configuration. Second, we demonstrate that an oligonucleotide-linked, long-wavelength cFRET configuration has energy transfer similar to an analogous peptide-linked configuration, where the oligonucleotide-linked cFRET configuration can be combined with toehold-mediated strand displacement for the multiplexed detection of unlabeled nucleic acid targets as a single vector. Overall, this work establishes the general applicability of cFRET and introduces new strategies for its bioanalytical application.