脱氧核酶
荧光团
铀酰
选择性
化学
水溶液中的金属离子
铀
检出限
荧光
光化学
基质(水族馆)
催化作用
金属
材料科学
离子
色谱法
生物化学
有机化学
物理
海洋学
量子力学
冶金
地质学
作者
Juewen Liu,Andrea K. Brown,Xiangli Meng,Donald M. Cropek,Jonathan D. Istok,David B. Watson,Yi Lu
标识
DOI:10.1073/pnas.0607875104
摘要
Here, we report a catalytic beacon sensor for uranyl (UO 2 2+ ) based on an in vitro -selected UO 2 2+ -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 2 2+ 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 ≈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.
科研通智能强力驱动
Strongly Powered by AbleSci AI