catalytic beacon sensor for uranium with parts-per-trillion sensitivity and millionfold selectivity

Here, we report a catalytic beacon sensor for uranyl (UO[Formula: see text]) based on an in vitro-selected UO[Formula: see text]-specific DNAzyme. The sensor consists of a DNA enzyme strand with a 3' quencher and a DNA substrate with a ribonucleotide adenosine (rA) in the middle and a fluoropho...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 2007-02, Vol.104 (7), p.2056-2061
Hauptverfasser: Liu, Juewen, Brown, Andrea K, Meng, Xiangli, Cropek, Donald M, Istok, Jonathan D, Watson, David B, Lu, Yi
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Sprache:eng
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Zusammenfassung:Here, we report a catalytic beacon sensor for uranyl (UO[Formula: see text]) based on an in vitro-selected UO[Formula: see text]-specific DNAzyme. The sensor consists of a DNA enzyme strand with a 3' quencher and a DNA substrate with a ribonucleotide adenosine (rA) in the middle and a fluorophore and a quencher at the 5' and 3' ends, respectively. The presence of UO[Formula: see text] causes catalytic cleavage of the DNA substrate strand at the rA position and release of the fluorophore and thus dramatic increase of fluorescence intensity. The sensor has a detection limit of 11 parts per trillion (45 pM), a dynamic range up to 400 nM, and selectivity of >1-million-fold over other metal ions. The most interfering metal ion, Th(IV), interacts with the fluorescein fluorophore, causing slightly enhanced fluorescence intensity, with an apparent dissociation constant of [almost equal to]230 μM. This sensor rivals the most sensitive analytical instruments for uranium detection, and its application in detecting uranium in contaminated soil samples is also demonstrated. This work shows that simple, cost-effective, and portable metal sensors can be obtained with similar sensitivity and selectivity as much more expensive and sophisticated analytical instruments. Such a sensor will play an important role in environmental remediation of radionuclides such as uranium.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.0607875104