Abstract
A surface-enhanced Raman scattering (SERS) method is proposed for the assay of microRNA 122 based on configuration change of DNA tetrahedron. Firstly, a DNA tetrahedron was self-assembled with one vertex labeled with toluidine blue (TB). Then, it was immobilized on the porous Ni/SiO2@PEI@Au as a SERS platform, which was characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD). At this time, the DNA tetrahedron was contracted; so, the TB is close to AuNPs and the Raman signal is high. When target microRNA 122 existed, with the nicking enzyme amplification strategy, a great deal of DNA signal chains (S5) was obtained, which can extend the contracted DNA tetrahedron and change it into a three-dimensional DNA tetrahedron. In this case, the TB was far from AuNPs, resulting in a lower Raman signal. Due to the configuration change of DNA tetrahedron, the Raman signal at 1624 cm−1 (with the excitation wavelength of 633 nm) has a linear relationship with the logarithm concentration of microRNA 122. This SERS assay has high sensitivity for microRNA 122 with a determination range from 0.01 aM to 10 fM and a detection limit of 0.009 aM. The recoveries from spiked samples were in the range 95 to 109%. This SERS strategy is designed based on the target-triggered configuration change of DNA tetrahedron, which can give new insight for DNA structures in bioanalysis.
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Acknowledgments
This work was supported by the Chongqing Research Program of Basic Research and Frontier Technology (cstc2019jcyj-msxmX0209), Fundamental Research Funds for the Central Universities (XDJK2019C077), Open Project Program of College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology (QUSTHX201804).
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The authors also thank Xia Zhong (Southwest University) for the Raman test technical support.
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Wang, S., Wu, C., Luo, J. et al. Target-triggered configuration change of DNA tetrahedron for SERS assay of microRNA 122. Microchim Acta 187, 460 (2020). https://doi.org/10.1007/s00604-020-04449-7
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DOI: https://doi.org/10.1007/s00604-020-04449-7