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Sensitive detection of prion protein through long range resonance energy transfer between graphene oxide and molecular aptamer beacon

机译:通过氧化石墨烯和分子适体信标之间的长距离共振能量转移灵敏地检测病毒蛋白

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摘要

The traditional molecular aptamer beacon (MAB) is designed by combining an aptamer to a molecular beacon, and its two terminals are labelled with a fluorescent moiety (donor) and quenching moiety (acceptor), respectively. However, it usually has a high background because of the low energy transfer efficiency between the donor and the acceptor. In order to overcome these drawbacks, we have developed a novel MAB with just one fluorescently labelled end, which acts as the donor, and graphene oxide (GO) introduced as the acceptor for target detection by employing long range resonance energy transfer (LrRET) as the signal-transduction mechanism from GO to MAB. To test the validity of the designed MAB system, cellular prion protein (PrP~c) has been used as the model target. It was found that the fluorescence of the designed MAB is completely quenched by GO, supplying a very low background. Conversely, the quenched fluorescence is recovered significantly with the addition of PrP~c, so that PrP~c can be detected over a wide range of 10.2-78.8 ng mL~(-1) with a detection limit as low as 0.309 u.g mL~(-1) and with high selectivity. This GO-based MAB approach is a successful application of LrRET for the detection of PrP~c, with advantages such as low costs, high quenching efficiency and good specificity, and it opens up new opportunities for the sensitive detection of biorecognition events.
机译:传统的分子适体信标(MAB)是通过将适体与分子信标结合而设计的,其两个末端分别标记有荧光部分(供体)和猝灭部分(受体)。但是,由于供体和受体之间的能量转移效率低,因此通常具有较高的本底。为了克服这些缺点,我们开发了一种新型的MAB,它只有一个荧光标记的末端作为供体,通过引入长距离共振能量转移(LrRET)作为目标检测的受体引入了氧化石墨烯(GO)。从GO到MAB的信号传导机制。为了测试设计的MAB系统的有效性,已将细胞病毒蛋白(PrP〜c)用作模型目标。发现所设计的MAB的荧光被GO完全淬灭,提供了非常低的背景。相反,加入PrP〜c可以显着回收猝灭的荧光,因此可以在10.2-78.8 ng mL〜(-1)的宽范围内检测到PrP〜c,检出限低至0.309 ug mL〜。 (-1)且具有高选择性。这种基于GO的MAB方法是LrRET在PrP〜c检测中的成功应用,具有成本低,淬灭效率高和特异性好等优点,为灵敏地检测生物识别事件开辟了新的机会。

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