Duan Nuo, Wu Shijia, Ma Xiaoyuan, Xia Yu, Wang Zhouping
State Key Laboratory of Food Science and Technology, Synergetic Innovation Center of Food Safety and Nutrition, School of Food Science and Technology, Jiangnan University, Wuxi 214122, China.
State Key Laboratory of Food Science and Technology, Synergetic Innovation Center of Food Safety and Nutrition, School of Food Science and Technology, Jiangnan University, Wuxi 214122, China.
Anal Biochem. 2014 Jun 1;454:1-6. doi: 10.1016/j.ab.2014.03.005. Epub 2014 Mar 17.
We report a universal fluorescent aptasensor based on the AccuBlue dye, which is impermeant to cell membranes, for the detection of pathogenic bacteria. The sensor consists of AccuBlue, an aptamer strand, and its complementary strand (cDNA) that partially hybridizes to the aptamer strand. We have fabricated two models by changing the sequence of the reaction between the elements in the system. One is the "signal on" model in which the aptamer is first bound to the target, followed by the addition of cDNA and AccuBlue, at which time the cDNA hybridizes with the free unreacted aptamer and forms a double-stranded DNA (dsDNA) duplex. Such hybridization causes AccuBlue to insert into the dsDNA and exhibit significantly increased fluorescence intensity because of the specific intercalation of the AccuBlue into dsDNA rather than single-stranded DNA (ssDNA). The other model, "signal off," involves hybridization of the aptamer with cDNA first, resulting in high fluorescence intensity on the addition of AccuBlue. When the target is added, the aptamer binds the target, causing the cDNA to detach from the dsDNA duplex and resulting in low fluorescence as a result of the liberation of AccuBlue. Because this design is based purely on DNA hybridization, and AccuBlue is impermeant to cell membranes, it could potentially be adapted to a wide variety of analytes.
我们报道了一种基于AccuBlue染料的通用荧光适体传感器,用于检测病原菌,AccuBlue染料不能透过细胞膜。该传感器由AccuBlue、一条适体链及其互补链(cDNA)组成,互补链与适体链部分杂交。我们通过改变系统中各元素之间的反应顺序构建了两种模型。一种是“信号开启”模型,即适体首先与靶标结合,然后加入cDNA和AccuBlue,此时cDNA与游离的未反应适体杂交,形成双链DNA(dsDNA)双链体。这种杂交使AccuBlue插入dsDNA中,并由于AccuBlue特异性插入dsDNA而非单链DNA(ssDNA)而表现出显著增加的荧光强度。另一种模型“信号关闭”,首先是适体与cDNA杂交,加入AccuBlue后产生高荧光强度。当加入靶标时,适体与靶标结合,导致cDNA从dsDNA双链体上脱离,由于AccuBlue的释放而导致荧光强度降低。由于这种设计纯粹基于DNA杂交,且AccuBlue不能透过细胞膜,因此它有可能适用于多种分析物。