Ultrasensitive SERS detection of Bacillus thuringiensis special gene based on Au@Ag NRs and magnetic beads

被引:55
|
作者
Wu, Long [1 ]
Xiao, Xiaoyan [1 ]
Chen, Kun [1 ]
Yin, Wenmin [1 ]
Li, Qin [1 ]
Wang, Pan [1 ]
Lu, Zhicheng [1 ]
Ma, Jing [1 ]
Han, Heyou [1 ]
机构
[1] Huazhong Agr Univ, Coll Food Sci & Technol, Coll Sci, State Key Lab Agr Microbiol, Wuhan 430070, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Surface Raman enhanced scatting; Magnetic beads; Bacillus thuringiensis transgene; Au-Ag core-shell nanorods; ENHANCED RAMAN-SPECTROSCOPY; SENSITIVE DETECTION; AMPLIFIED DETECTION; GOLD NANOPARTICLES; DNA SENSOR; SURFACE; SHELL; CORE; SCATTERING; NANORODS;
D O I
10.1016/j.bios.2016.11.005
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
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 0.1 pM to 1 nM with a detection limit of 0.14 pM (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.
引用
收藏
页码:321 / 327
页数:7
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