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首页> 外文期刊>Analytical Biochemistry: An International Journal of Analytical and Preparative Methods >DNA-silver nanocluster probe for norovirus RNA detection based on changes in secondary structure of nucleic acids
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DNA-silver nanocluster probe for norovirus RNA detection based on changes in secondary structure of nucleic acids

机译:基于核酸二次结构的变化,DNA-银纳米粉探针用于诺病毒RNA检测

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摘要

DNA-templated silver nanoclusters (DNA-AgNCs) is a kind of fluorescent nanoclusters in-situ synthesized on DNA, thereby giving the DNA probe an inherent function of label-free signal output. Herein, the DNA-AgNCs with a GCC-loop-structure which has a quantum field of 51.6% was firstly proposed. It was proved that the addition of the double-stranded structure on the GCC-loop drastically enhanced the fluorescence intensity of the AgNCs. Through the further studies of the relationship between DNA secondary structure and AgNCs, a kind of DNA-AgNCs-probe was designed based on the change of the secondary structure which was induced by the target strand. By this, the fluorescence signal of probe was in "turn on" mode. The probe system could be directly used for the detection of Norovirus RNA, which had a linearity of 20 nM to 1.8 mu M with a detection limit of 18 nM. Moreover, this detection platform was also selective to differentiate mismatched RNA. It was expected to be a universal method for different RNA detection by changing the recognition sequence of the probe.
机译:DNA模板化银纳米蛋白(DNA-AGNC)是在DNA上合成的原位原位的一种荧光纳米团簇,从而使DNA探测无标记信号输出的固有函数。在此,首先提出了具有51.6%的量子场的GCC环结构的DNA-AGNC。事实证明,在GCC环上加入双链结构大大提高了AGNC的荧光强度。通过进一步研究DNA二级结构与AGNC之间的关系,基于由靶链诱导的二级结构的变化设计了一种DNA-AGNCS探针。由此,探针的荧光信号在“开启”模式下。探针系统可以直接用于检测诺病毒RNA,其线性度为20nm至1.8μm,检测限为18nm。此外,该检测平台也选择性以区分不匹配的RNA。预计通过改变探针的识别序列来成为不同RNA检测的普遍方法。

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