Detection of Hg ²⁺ Using a Dual-Mode Biosensing Probe Constructed Using Ratiometric Fluorescent Copper Nanoclusters@Zirconia Metal-Organic Framework/ N -Methyl Mesoporphyrin IX and Colorimetry G-Quadruplex/Hemin Peroxidase-Mimicking G-Quadruplex DNAzyme

Abstract

Mercury (Hg 2+ ) has been recognized as a global pollutant with a toxic, mobile, and persistent nature. It adversely affects the ecosystem and human health. Already developed biosensors for Hg 2+ detection majorly suffer from poor sensitivity and specificity. Herein, a colorimetric/fluorimetric dual-mode sensing approach is designed for the quantitative detection of Hg 2+ . This novel sensing approach utilizes nanofluorophores, i.e., fluorescent copper nanoclusters-doped zirconia metal-organic framework (CuNCs@Zr-MOF) nanoconjugate (blue color) and N -methyl mesoporphyrin IX (NMM) (red color) in combination with peroxidase-mimicking G-quadruplex DNAzyme (PMDNAzyme). In the presence of Hg 2+ , dabcyl conjugated complementary DNA with T–T mismatches form the stable duplex with the CuNCs@Zr-MOF@G-quadruplex structure through T–Hg 2+ –T base pairing. It causes the quenching of fluorescence of CuNCs@Zr-MOF (463 nm) due to the Förster resonance energy transfer (FRET) system. Moreover, the G-quadruplex (G4) structure of the aptamer enhances the fluorescence emission of NMM (610 nm). Besides this, the peroxidase-like activity of G4/hemin DNAzyme offers the colorimetric detection of Hg 2+ . The formation of duplex with PMDNAzyme increases the catalytic activity. This novel biosensing probe quantitatively detected Hg 2+ using both fluorimetry and colorimetry approaches with a low detection limit of 0.59 and 36.3 nM, respectively. It was also observed that the presence of interfering metal ions in case of real aqueous samples does not affect the performance of this novel biosensing probe. These findings confirm the considerable potential of the proposed biosensing probe to screen the concentration of Hg 2+ in aquatic products.