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A label-free and enzyme-free aptasensor for visual Cd2+ detection based on split DNAzyme fragments

机译:基于标记的DNAzyme片段的无标记和无酶适体传感器,用于视觉Cd2 +检测

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A label-free and enzyme-free three-way junction sensing system has been proposed for the amplified detection of Cd2+ based on split G-quadruplex DNAzyme fragments. Three hairpin structures were designed as the building blocks (hairpins 1, 2, and 3) to construct the three-way G-quadruplex junction. In the presence of Cd2+, the combination of Cd2+ and the aptamer initiated branch migration of hairpins to form an unstable complex. Then Cd2+–aptamer dissociated from the complex, acting as a catalyst to trigger the hybridization of additional branched junctions. Thus, the 3?:?1 split G-quadruplex fragments of those hairpins were brought into close-enough proximity to form a G-quadruplex. After addition of hemin, numerous intact G-quadruplex/hemin DNAzymes were generated, leading to an intensified color change observed by the naked eye. The biosensor exhibits excellent selectivity and high sensitivity for Cd2+ with a detection limit as low as 10 pM. The biosensor is simple and convenient in operation without labeling, washing, and modification, which makes it suitable for routine monitoring of Cd2+.
机译:已经提出了一种无标记和无酶的三向连接感应系统,用于基于分裂的G-四链体DNA酶片段的Cd2 +扩增检测。设计了三个发夹结构作为构建块(发夹1、2和3),以构造三向G-四联体连接。在Cd2 +存在下,Cd2 +和适体的结合会引发发夹的分支迁移,从而形成不稳定的复合物。然后,Cd2 +-适体从复合物中解离,充当催化剂来触发其他分支连接的杂交。因此,将这些发夹的3′∶13的分裂的G-四链体片段紧密接近以形成G-四链体。加入血红素后,产生了许多完整的G-四链体/血红素DNA酶,导致肉眼观察到颜色增强。该生物传感器对Cd2 +表现出出色的选择性和高灵敏度,检测限低至10 pM。该生物传感器操作简单方便,无需标记,清洗和修饰,因此适用于Cd2 +的常规监测。

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