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首页> 外文期刊>Analytical methods >Fluorescent detection of Mucin 1 protein based on aptamer functionalized biocompatible carbon dots and graphene oxide
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Fluorescent detection of Mucin 1 protein based on aptamer functionalized biocompatible carbon dots and graphene oxide

机译:基于适体功能化的生物相容性碳点和氧化石墨烯的Mucin 1蛋白荧光检测

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摘要

An ultrasensitive aptasensor for the detection of Mucin 1 (MUC1) protein based on fluorescence resonance energy transfer (FRET) between carbon dots (CDs) and graphene oxide (GO) is reported herein. Taking advantage of the strong fluorescence and good biocompatibility of CDs, the MUC1 aptamer was covalently conjugated to CDs (aptamer-CDs) to capture MUC1 protein through high affinity interaction between the aptamer and MUC1 protein. The FRET process between the aptamer-CDs and GO is easily achieved due to their efficient self-assembly through specific pi-pi interaction, in which the fluorescence of CDs was efficiently quenched. In the presence of the target MUC1 protein, the association constant between aptamer-CDs and MUC1 is bigger than that between aptamer-CDs and GO, leading to the release of the aptamer-CDs from GO, resulting in the recovery of the fluorescence of CDs. This aptamer was observed to detect MUC1 protein specifically and sensitively in a linear range from 20.0 to 804.0 nM with a detection limit of 17.1 nM. The developed aptasensor is highly biocompatible and nontoxic, which can be easily modified for the detection of other protein biomarker.
机译:本文报道了一种基于碳点(CD)和氧化石墨烯(GO)之间的荧光共振能量转移(FRET)用于检测粘蛋白1(MUC1)蛋白的超灵敏适体传感器。利用CD的强荧光和良好的生物相容性,将MUC1适体共价偶联到CD(适体CD)上,以通过适体与MUC1蛋白之间的高亲和力相互作用捕获MUC1蛋白。适体CD和GO之间的FRET过程很容易实现,这是因为它们通过特定的pi-pi相互作用实现了高效的自组装,从而有效地猝灭了CD的荧光。在目标MUC1蛋白存在下,适体-CD和MUC1之间的缔合常数大于适体-CD和GO之间的缔合常数,导致适体-CD从GO释放,导致CD的荧光恢复。观察到该适体可特异性和灵敏地在20.0至804.0 nM的线性范围内检测MUC1蛋白,检测限为17.1 nM。研发的适体传感器具有高度的生物相容性且无毒,可以轻松修改以检测其他蛋白质生物标志物。

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