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Exonuclease III assisted aptasensor for adenosine detection with gold nanoparticle probes

机译:核酸外切酶III辅助的适体传感器与金纳米颗粒探针一起检测腺苷

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Herein, a gold nanoparticle (GNP)-based colorimetric aptasensor has been developed for detecting adenosine with exonuclease III (Exo III) assisted recycling amplification. In this aptasensor, two kinds of single-stranded oligonucleotide functionalized GNP probes (Oligo 1-GNPs and Oligo 2-GNPs) are firstly hybridized with one complementary single-stranded oligonucleotide (linker) with the motif of adenosine aptamer, resulting in the formation of GNP aggregates (cross-linked GNPs). In the presence of adenosine, the linker would form a double-stranded DNA (dsDNA) with a recessed 3a€2-terminus due to its structural switching property, which would lead to disassembly of the cross-linked GNPs. However, upon the addition of Exo III, the dsDNA is enzymatically digested from the 3a€2-hydroxyl termini, liberating the adenosine. The released adenosine can then interact with another linker and a new round of enzymatic digestion is started. Therefore, remarkable signal amplification is achieved because the disassembly of cross-linked GNPs is strongly dependent on the free adenosine in the reaction mixture. The experimental results demonstrate that the Exo III-assisted GNP-based colorimetric aptasensor is more sensitive (ca. 10 times) than that without Exo III amplification. The Exo III-assisted GNP-based colorimetric aptasensor detects adenosine downs to 5.6 nM, with a linear relationship from 10 nM to 1 mM. Moreover, the Exo III-assisted GNP-based colorimetric aptasensor has been successfully applied to detect Jinshuibao capsule (JSBC) containing adenosine in both a buffer solution and a diluted human serum, demonstrating that this assay has great potential to be employed for detecting adenosine in real samples.
机译:本文中,已经开发了基于金纳米颗粒(GNP)的比色适体传感器,用于利用核酸外切酶III(Exo III)辅助循环扩增检测腺苷。在这种适体传感器中,首先将两种单链寡核苷酸功能化的GNP探针(Oligo 1-GNP和Oligo 2-GNP)与一个带有腺苷适体的互补单链寡核苷酸(接头)杂交,从而形成GNP聚集体(交联的GNP)。在存在腺苷的情况下,由于其结构转换特性,接头将形成带有凹入的3a€2-末端的双链DNA(dsDNA),这将导致交联的GNP分解。但是,添加Exo III后,会从3a€2-羟基末端酶切消化dsDNA,从而释放出腺苷。然后,释放的腺苷可以与另一个接头相互作用,并开始新一轮的酶消化。因此,由于交联的GNP的分解强烈依赖于反应混合物中的游离腺苷,因此可实现显着的信号放大。实验结果表明,Exo III辅助的基于GNP的比色适体传感器比没有Exo III扩增的传感器更灵敏(约10倍)。 Exo III辅助的基于GNP的比色适体传感器检测到腺苷降到5.6 nM,线性关系从10 nM到1 mM。此外,Exo III辅助的基于GNP的比色适体传感器已成功应用于检测缓冲液和稀释的人血清中均含有腺苷的金水宝胶囊(JSBC),表明该测定法具有很大的潜力可用于检测人体中的腺苷。真实样本。

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