Abstract
A colorimetric method was developed using G-quadruplex and gold nanoparticles (AuNPs) for determination of Escherichia coli K88 (ETEC K88). It was composed of two modules: (1) an aptamer as biorecognizing element and (2) a capturing DNA (modified with AuNPs at 5′) as a transducer. In the absence of target bacteria, the aptamer can form stable double strands with capturing DNA, preventing the binding of capturing DNA to the G-quadruplex. However, the double strands of capturing DNA and aptamer are untied due to the stronger binding of aptamers to bacteria in the presence of target bacteria. As a result, the G-quadruplex binds to capture DNA and leads to the aggregation and color change of AuNPs, which can be monitored by a spectrophotometer or visualization. The quantitative determination was achieved by monitoring the optical density change of AuNPs solution at 524 nm after target addition. Under optimal conditions, the method has a low detection limit (1.35 × 102 CFU mL−1) and a linear response in the range 102 to 106 CFU mL−1.
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Funding
This work was supported by National Natural Science Foundation of China (31770109), the Opening Fund of Key Laboratory of Chemical Biology and Traditional Chinese Medicine Research (Hunan Normal University), Ministry of Education (KLCBTCMR18-03), project funded by China Postdoctoral Science Foundation (2018 M640753), and Hunan Provincial Innovation Foundation for Postgraduate (CX20190392).
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Wang, Z., Lu, Q., Xu, T. et al. G-quadruplex-based assay combined with aptamer and gold nanoparticles for Escherichia coli K88 determination. Microchim Acta 187, 308 (2020). https://doi.org/10.1007/s00604-020-04291-x
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DOI: https://doi.org/10.1007/s00604-020-04291-x