Issue 10, 2006

Combinatorial fluorescence energy transfer molecular beacons for probing nucleic acid sequences

Abstract

We report the design, synthesis, and characterization of molecular beacons (MB) consisting of three distinct fluorophores, 6-carboxyfluorescein (Fam), N,N,N′,N′-tetramethyl-6-carboxyrhodamine (Tam), and Cyanine-5 (Cy5). The primary light absorber/energy donor (Fam) is located on one terminus of the MB, whereas the primary energy acceptor/secondary donor (Tam) and secondary acceptor (Cy5) are located at the other terminus of the MB. In the absence of target DNA or RNA, the MB exists in the stem-closed form. Excitation of Fam initiates an energy transfer cascade from Fam to Tam and further to Cy5 generating unique fluorescence signatures defined as the ratio of the emission from each of the three fluorophores. This energy transfer cascade was investigated in detail by steady-state and time-resolved fluorescence spectroscopy, as well as fluorescence depolarization studies. In the presence of the complementary target DNA, the MB opened efficiently and hybridized with the target separating Fam and Tam by a large distance, so that energy transfer from Fam to Tam was blocked in the stem-open form. This opening of the MB generates a “bar code” fluorescence signature, which is different from the signature of the stem-closed MB. The fluorescence signature of this combinatorial fluorescence energy transfer MB can be tuned by variation of the spacer length between the individual fluorophores.

Graphical abstract: Combinatorial fluorescence energy transfer molecular beacons for probing nucleic acid sequences

Article information

Article type
Paper
Submitted
26 Apr 2006
Accepted
28 Jun 2006
First published
12 Jul 2006

Photochem. Photobiol. Sci., 2006,5, 896-902

Combinatorial fluorescence energy transfer molecular beacons for probing nucleic acid sequences

X. Li, Z. Li, A. A. Martí, S. Jockusch, N. Stevens, D. L. Akins, N. J. Turro and J. Ju, Photochem. Photobiol. Sci., 2006, 5, 896 DOI: 10.1039/B605936H

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