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OFF-to-ON type fluorescent probe for the detection of 8-oxo-dG in DNA by the Adap-masked ODN probe. | LitMetric

OFF-to-ON type fluorescent probe for the detection of 8-oxo-dG in DNA by the Adap-masked ODN probe.

Bioorg Med Chem Lett

Graduate School of Pharmaceutical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.

Published: January 2012

AI Article Synopsis

  • Researchers have developed a new fluorescence resonance energy transfer (FRET) probe using Adap, which is an artificial nucleoside that can specifically bond through multiple hydrogen bonds and is selectively quenched by 8-oxo-2'-deoxyguanosine (8-oxo-dG) in DNA.
  • The probe consists of two strands: one with Adap and the other with natural nucleotides, designed to create a less stable double strand that initially shows quenching of fluorescence due to FRET.
  • When 8-oxo-dG is present in the complementary DNA strand, it enhances the separation of the duplex probe, leading to fluorescence recovery and demonstrating the probe’s ability to distinguish between 8-oxo-dG and regular de

Article Abstract

We have recently reported that Adap (adenosine-1,3-diazaphenoxazine) is an artificial nucleoside analogue for the specific recognition by multiple hydrogen bonding and that its fluorescence is selectively quenched with 8-oxo-2'-deoxyguanosine (8-oxo-dG) in DNA. We now report the development of a new OFF-to-ON type FRET probe, in which one strand contains Adap and another contains natural nucleotides for the formation of a less stable double strand. Each strand was labeled with Cy3 or BHQ2 at the 5'-end or 3'-end, respectively. It was expected in this system that fluorescence of the duplex probe is first quenched by FRET, but the target DNA strand containing 8-oxo-dG at the complementary site of Adap would enhance the displacement reaction of the less stable duplex probe that results in the fluorescence recovery. The results showed that the duplex probe containing the Adap-T base pair exhibited a complete discrimination between 8-oxo-dG and dG in DNA by fluorescence enhancement.

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Source
http://dx.doi.org/10.1016/j.bmcl.2011.10.093DOI Listing

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