School of Grain Science and Technology, Jiangsu University of Science and Technology, Zhenjiang, 212003, China.
Key Laboratory of Modern Agriculture Equipment and Technology, School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang, 212013, China.
Talanta. 2020 May 15;212:120764. doi: 10.1016/j.talanta.2020.120764. Epub 2020 Jan 20.
A magnetic-separation-dual-targets fluorescent biosensor was fabricated to detect terminator nopaline synthase (TNOS) and promoter of cauliflower mosaic virus 35s (P35S) in transgenic soybean based on incorporation of bicolor CdTe quantum dots carried by silica nanospheres. In this protocol, the fixed probes for TNOS or P35S were magnetized firstly with FeO@Au magnetic nanosphere by Au-S covalent bonding to achieve magnetized probes. Meanwhile, the capture probes for TNOS or P35S were functionalized with green or red fluorescent microspheres respectively to obtain fluorescently-labeled probes, which could emit relative strong green or red fluorescent signal. Two terminals of TNOS or P35S were recognized by magnetized probes and fluorescently-labeled probes respectively to form the sandwiched structures in the process of biosensor development subsequently, and it was separated by a magnet instantly. The fluorescence intensities of remnant supernatant were measured and analyzed accordingly to achieve simultaneous detection of TNOS and P35S. This biosensor exhibited a good dynamic range, low limit of detection and excellent selectivity in detecting transgenic soybean.
一种基于双靶向荧光磁分离生物传感器的构建方法,用于检测转大豆中终止子胭脂碱合成酶(TNOS)和花椰菜花叶病毒 35S 启动子(P35S)。该方法将双载色CdTe 量子点修饰到硅纳米球中,利用 Au-S 共价键将固定探针(TNOS 或 P35S)磁化为磁探针,同时将捕获探针(TNOS 或 P35S)分别功能化到绿色或红色荧光微球上,得到荧光标记探针,分别发出相对较强的绿色或红色荧光信号。TNOS 或 P35S 的两个末端分别被磁探针和荧光标记探针识别,从而在生物传感器的开发过程中形成夹心结构,随后立即用磁铁将其分离。测量并分析剩余上清液的荧光强度,从而实现 TNOS 和 P35S 的同时检测。该生物传感器在检测转大豆时表现出良好的动态范围、较低的检测限和优异的选择性。