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Water-soluble mercury ion sensing based on the thymine-Hg2+-thymine base pair using retroreflective Janus particle as an optical signaling probe
Biosensors and Bioelectronics ( IF 10.7 ) Pub Date : 2018-01-06 , DOI: 10.1016/j.bios.2018.01.008
Hyeong Jin Chun , Saemi Kim , Yong Duk Han , Dong Woo Kim , Ka Ram Kim , Hyo-Sop Kim , Jae-Ho Kim , Hyun C. Yoon

Herein, we report an optical sensing platform for mercury ions (Hg2+) in water based on the integration of Hg2+-mediated thymine-thymine (T-T) stabilization, a biotinylated stem-loop DNA probe, and a streptavidin-modified retroreflective Janus particle (SA-RJP). Two oligonucleotide probes, including a stem-loop DNA probe and an assistant DNA probe, were utilized. In the absence of Hg2+, the assistant DNA probe does not hybridize with the stem-loop probe due to their T-T mismatch, so the surface-immobilized stem-loop DNA probe remains a closed hairpin structure. In the presence of Hg2+, the DNA forms a double-stranded structure with the loop region via Hg2+-mediated T-T stabilization. This DNA hybridization induces stretching of the stem-loop DNA probe, exposing biotin. To translate these Hg2+-mediated structural changes in DNA probe into measurable signal, SA-RJP, an optical signaling label, is applied to recognize the exposed biotin. The number of biospecifically bound SA-RJPs is proportional to the concentration of Hg2+, so that the concentration of Hg2+ can be quantitatively analyzed by counting the number of RJPs. Using the system, a highly selective and sensitive measurement of Hg2+ was accomplished with a limit of detection of 0.027 nM. Considering the simplified optical instrumentation required for retroreflection-based RJP counting, RJP-assisted Hg2+ measurement can be accomplished in a much easier and inexpensive manner. Moreover, the detection of Hg2+ in real drinking water samples including tap and commercial bottled water was successfully carried out.



中文翻译:

基于胸腺嘧啶-Hg 2 +-胸腺嘧啶碱基对的水溶性汞离子感测,使用逆反射Janus粒子作为光信号探针

在此,我们报告了一个基于Hg 2+介导的胸腺嘧啶-胸腺嘧啶(TT)稳定化,生物素化茎环DNA探针和链霉亲和素修饰的逆向反射的集成的水中汞离子(Hg 2+)的光学传感平台。Janus粒子(SA-RJP)。使用了两个寡核苷酸探针,包括茎环DNA探针和辅助DNA探针。在没有Hg 2+的情况下,辅助DNA探针由于TT不匹配而不会与茎环探针杂交,因此表面固定的茎环DNA探针保持闭合的发夹结构。在存在Hg 2+的情况下,DNA通过Hg 2+与环区形成双链结构-介导的TT稳定化。这种DNA杂交诱导了茎环DNA探针的拉伸,从而暴露了生物素。为了将这些Hg 2+介导的DNA探针结构变化转化为可测量的信号,应用SA-RJP(一种光学信号标记)来识别暴露的生物素。生物特异性结合的SA-RJPs的数量与Hg 2+的浓度成正比,因此可以通过计算RJPs的数量来定量分析Hg 2+的浓度。使用该系统,可以以0.027 nM的检出限实现对Hg 2+的高度选择性和灵敏的测量。考虑到基于回反射的RJP计数所需的简化光学仪器,RJP辅助的Hg 2+可以以更容易和便宜的方式完成测量。此外,成功进行了包括自来水和商业瓶装水在内的实际饮用水样品中Hg 2+的检测。

更新日期:2018-01-06
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