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A novel exonuclease III-aided amplification assay based on a graphene platform for sensitive detection of adenosine triphosphate

机译:基于石墨烯平台的新型核酸外切酶III辅助扩增检测用于三磷酸腺苷的灵敏检测

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We have developed a novel exonuclease III (Exo III)-aided amplification assay based on a graphene platform for sensitive detection of adenosine triphosphate (ATP). This system consists of fluorescein isothiocyanate (FITC)-labeled ATP aptamers, graphene and Exo III. In the presence of target ATP, the target molecule binding the aptamer leads to the formation of aptamera€“target complexes. Subsequently, Exo III selectively catalyzes the stepwise removal of mononucleotides from aptamera€“target complexes, resulting in the removal of FITC and the release of target ATP. The released target ATP then binds with another FITC-labeled ATP aptamer probe, and the cycle starts anew, resulting in the continuous cleavage of aptamera€“target complexes. Consequently, each target ATP can initiate the cleavage of many FITC-labeled ATP aptamer probes, generating a concomitant increase in the fluorescence. Finally, graphene is added to quench the fluorescence of rudimental FITC-labeled aptamer probes, and the fluorescence from the free FITC is detected. With this approach, the fluorescence intensity of the system increases with the increase in the concentration of ATP over a range of 10a€“1000 nM with a detection limit of 5 nM. The present method was successfully applied for the detection of ATP in human serum.
机译:我们已经开发了一种基于石墨烯平台的新型核酸外切酶III(Exo III)辅助扩增测定法,用于三磷酸腺苷(ATP)的灵敏检测。该系统由荧光素异硫氰酸酯(FITC)标记的ATP适体,石墨烯和Exo III组成。在靶ATP的存在下,结合适体的靶分子导致形成适体靶复合物。随后,Exo III选择性催化从适体靶标复合物中逐步去除单核苷酸,从而去除FITC和释放靶标ATP。然后,释放的靶ATP与另一个FITC标记的ATP适体探针结合,并且该循环重新开始,从而导致适体靶复合物的连续裂解。因此,每种靶ATP均可引发许多FITC标记的ATP适体探针的裂解,从而伴随荧光的增加。最后,添加石墨烯以淬灭基本FITC标记的适体探针的荧光,并检测来自游离FITC的荧光。使用这种方法,系统的荧光强度随着ATP浓度的增加而增加,范围为10a” -1000 nM,检测极限为5 nM。本方法已成功应用于人血清中ATP的检测。

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