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A highly sensitive and selective fluorescent probe without quencher for detection of Pb(2+) ions based on aggregation-caused quenching phenomenon

Lead is a highly toxic heavy metal, and various functional nucleic acid (FNA)-based biosensors have been developed for the detection of Pb(2+) in environmental monitoring. However, most fluorescence biosensors that have been reported were designed on the basis of a double-labeled (fluorophore and qu...

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Detalles Bibliográficos
Autores principales: Li, Qianyun, Jia, Yongmei, Feng, Zongcai, Liu, Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9090614/
https://www.ncbi.nlm.nih.gov/pubmed/35558300
http://dx.doi.org/10.1039/c8ra07903j
Descripción
Sumario:Lead is a highly toxic heavy metal, and various functional nucleic acid (FNA)-based biosensors have been developed for the detection of Pb(2+) in environmental monitoring. However, most fluorescence biosensors that have been reported were designed on the basis of a double-labeled (fluorophore and quencher group) DNA sequence, which not only involved an inconvenient organic synthesis but also restricted their wider use in practical applications. Here, we utilized a G-rich DNA sequence as a recognition probe and conjugated fluorene (CF) to develop a fluorescence sensor without a quencher based on the aggregation-caused quenching (ACQ) effect. In the presence of Pb(2+), the degree of aggregation of CF was reduced because Pb(2+) induced the formation of a G-quadruplex structure of the CF-DNA probe, and the fluorescence signal increased with the concentration of Pb(2+) (0–1 μM), with a limit of detection of 0.36 nM. This fluorescent probe without a quencher enables the sensitive and selective detection of Pb(2+). On the basis of these advantages, the CF-DNA probe represents a promising analytical method for detecting Pb(2+).