| Literature DB >> 27839730 |
Long Wu1, Xiaoyan Xiao1, Kun Chen1, Wenmin Yin1, Qin Li1, Pan Wang1, Zhicheng Lu1, Jing Ma1, Heyou Han2.
Abstract
Highly sensitive and selective detection of specific DNA sequences is of great importance in clinical diagnosis, environmental and food monitoring, but it still remains challenges to develop a facile method for real sample detection in aqueous solution. Here, a simple and recyclable surface enhanced Raman scattering (SERS) sensor was constructed for Bacillus thuringiensis (Bt) special gene fragment detection by Fe3O4 magnetic beads (MBs) and Au-Ag core-shell nanorods (Au@Ag NRs). A hairpin DNA with sulfhydryl and biotin was attached to Au@Ag NRs as indicator, and MBs with streptavidin (SA) were acted as the capture probe. On the basis of the biotin-SA specific interaction, target sequences were first hybridized with the hairpin DNA and exposed the biotin. Subsequently, the Au@Ag NRs were captured by the streptavidin modified MBs, which reduced the suspended NRs and led to the change of Raman intensity. Under the optimal conditions, the SERS intensity revealed a good linearity with Bt transgene fragment ranging from 0.1pM to 1nM with a detection limit of 0.14pM (S/N=3). To demonstrate the specificity of the strategy, the single-base mismatch in DNA was discussed in the SERS assay. The results showed that the sensitivity and accuracy of the proposed method was acceptable in DNA detection, revealing a great potential in special gene detection.Entities:
Keywords: Au-Ag core-shell nanorods; Bacillus thuringiensis transgene; Magnetic beads; Surface Raman enhanced scatting
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Year: 2016 PMID: 27839730 DOI: 10.1016/j.bios.2016.11.005
Source DB: PubMed Journal: Biosens Bioelectron ISSN: 0956-5663 Impact factor: 10.618