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Programmable DNA Templates for Silver Nanoclusters Synthesis To Develop On-Demand FRET Aptasensor.
Liu, Yue; Hussain, Mustafa; Wang, Chengquan; Yang, Huiyuan; Wang, Kun; Wei, Jie; Long, Lingliang; Ding, Lijun; Qian, Jing.
Afiliación
  • Liu Y; School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang 212013, P. R. China.
  • Hussain M; School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang 212013, P. R. China.
  • Wang C; School of Food and Biological Engineering, Jiangsu University, Zhenjiang 212013, P. R. China.
  • Yang H; School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang 212013, P. R. China.
  • Wang K; School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang 212013, P. R. China.
  • Wei J; School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang 212013, P. R. China.
  • Long L; School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang 212013, P. R. China.
  • Ding L; School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang 212013, P. R. China.
  • Qian J; School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang 212013, P. R. China.
Anal Chem ; 96(25): 10391-10398, 2024 06 25.
Article en En | MEDLINE | ID: mdl-38844882
ABSTRACT
DNA-templated silver nanoclusters (AgNCs-DNA) can be synthesized via a one-pot method bypassing the tedious process of biomolecular labeling. Appending an aptamer to DNA templates results in dual-functionalized DNA strands that can be utilized for synthesizing aptamer-modified AgNCs, thereby enabling the development of label-free fluorescence aptasensors. However, a major challenge lies in the necessity to redesign the dual-functionalized DNA strand for each specific target, thus increasing the complexity and hindering widespread application of these aptasensors. To overcome this challenge, we designed six DNA strands (DNA1-DNA6) that incorporate the templates for AgNCs synthesis and A4-linker for further aptamer coupling. Among all the synthesized AgNCs-DNA samples, it was found that both AgNCs-DNA1 and AgNCs-DNA2 stood out for their excellent long-term stability. After capturing the T4-linker that connected with aptamer1 specific for aflatoxin B1 (AFB1), however, we found that only AgNCs-DNA1/aptamer1 maintained excellent long-term stability. This finding highlighted the potential of AgNCs-DNA1 as a versatile label-free fluorescence probe for the development of on-demand fluorescence aptasensors. To emphasize its benefits in aptasensing applications, we utilized AgNCs-DNA1/aptamer1 as the fluorescence probe and MoS2 nanosheets as the quencher to develop a FRET aptasensor for AFB1 detection. This aptasensor demonstrated remarkable sensitivity, enabling the detection of AFB1 within a wide concentration range of 0.03-120 ng/mL, with a limit of detection as low as 3.6 pg/mL (S/N = 3). The versatility of the aptasensor has been validated through the recognition of diverse targets, employing aptamer2 specific for ochratoxin A and aptamer3 specific for zearalenone, thereby showcasing its extensive applicability for on-demand detection. The universal applicability of this aptasensor holds great promise for future applications in diverse fields including food safety, environmental monitoring, and clinical diagnosis.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Técnicas Biosensibles Idioma: En Revista: Anal Chem Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Técnicas Biosensibles Idioma: En Revista: Anal Chem Año: 2024 Tipo del documento: Article