| Literature DB >> 18442293 |
Florian Menacher1, Moritz Rubner, Sina Berndl, Hans-Achim Wagenknecht.
Abstract
Thiazole orange was synthetically incorporated into oligonucleotides by using the corresponding phosphoramidite as the building block for automated DNA synthesis. Due to the covalent fixation of the TO dye as a DNA base surrogate, the TO-modified oligonucleotides do not exhibit a significant increase of fluorescence upon hybridization with the counterstrand. However, if 5-nitroindole (NI) is present as a second artificial DNA base (two base pairs away from the TO dye) a fluorescence increase upon DNA hybridization can be observed. That suggests that a short-range photoinduced electron transfer causes the fluorescence quenching in the single strand. The latter result represents a concept that can be transferred to the commercially available Cy3 label. It enables the Cy3 fluorophore to display the DNA hybridization by a fluorescence increase that is normally not observed with this dye.Entities:
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Year: 2008 PMID: 18442293 DOI: 10.1021/jo8004793
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354