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A genosensor for detection of HTLV-I based on photoluminescence quenching of fluorescent carbon dots in presence of iron magnetic nanoparticle-capped Au

机译:一种在铁磁性纳米粒子封端的Au存在下基于荧光碳点的光致发光猝灭检测HTLV-I的基因传感器

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Carbon dots and Fe3O4@Au were synthesized to develop a new biosensor to detect DNA target. We investigated the photoluminescence property of carbon dots (CDs) in the presence of Fe3O4-capped Au (Fe3O4@Au). Firstly, we designed two dedicated probes for unique long sequence region of human T-lymphotropic virus type 1 genome. One of the probes was covalently bound to the CDs. In the absence of target, CDs-probe was adsorbed on the surface of Fe3O4@Au through two possible mechanisms, leading to quenching the fluorescence emission of CDs. The fluorescence emission of CDs was recovered in the presence of target since double-stranded DNA cannot adsorb on the Fe3O4@Au. Also, Fe3O4@Au can adsorb the unhybridized oligonucleotides and improves the accuracy of detection. The specificity of the proposed biosensor was confirmed by BLAST search and assessed by exposing the biosensor to other virus targets. The experimental detection limit of the biosensor was below 10?nM with linear range from 10 to 320?nM.
机译:碳点和Fe3O4 @ Au被合成以开发一种新型生物传感器来检测DNA靶标。我们研究了在Fe3O4封端的Au(Fe3O4 @ Au)存在下碳点(CD)的光致发光特性。首先,我们设计了两种专用探针,用于人类T淋巴细胞病毒1型基因组的独特长序列区域。探针之一与CD共价结合。在没有靶标的情况下,CDs探针通过两种可能的机制吸附在Fe3O4 @ Au的表面上,从而导致CDs的荧光发射猝灭。由于双链DNA无法吸附在Fe3O4 @ Au上,因此在目标存在下可恢复CD的荧光发射。另外,Fe3O4 @ Au可以吸附未杂交的寡核苷酸,并提高检测精度。拟议的生物传感器的特异性通过BLAST搜索得到确认,并通过将生物传感器暴露于其他病毒靶标进行评估。生物传感器的实验检测极限低于10?nM,线性范围为10至320?nM。

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