Abstract

Since mercury is one of the most toxic heavy metals in water, its detection is critical for environmental protection. Various biosensors based on T-Hg2+-T sensing strategies have been developed; however, their mechanisms are highly dependent on the buffer conditions and are not suitable for the rapid high-throughput analysis of many complex water samples. In this work, a self-assembled biosensor for the high-throughput detection of Hg2+ based on a cleavable PS-RNA-modified probe and homogeneous photochemical chemiluminescence assay was developed. In the presence of Hg2+, the probe was cleaved, and the singlet oxygen channel was destroyed, which decreased the fluorescence signal. This biosensor is highly selective for Hg2+, with a limit of detection of 1.4 nM (S/N = 3) in a linear range of 5 nM - 5 μM (R2 = 0.991). The recoveries of standard addition methods in different water samples indicate that this feasible, simple method is a promising tool to monitor mercury ions in environmental applications.

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