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Self-Phosphorylating Deoxyribozyme Initiated Cascade Enzymatic Amplification for Guanosine-5'-triphosphate Detection

机译:自磷酸化脱氧核糖酶引发的级联酶促扩增的鸟苷-5'-三磷酸检测。

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摘要

The self-phosphorylating deoxyribozymes identified by in vitro selection can catalyze their own phosphorylation by utilizing phosphate donor guanosine-5'-triphosphate (GTP) which plays a critical role in a majority of cellular processes. On the basis of the unique properties of self-phosphorylating deoxyribozymes, we report a novel GTP sensor coupled with λ exonuclease cleavage reaction and nicking enzyme assisted fluorescence signal amplification process. The deoxyribozymes with special catalytic and structural characteristics display good stability compared to protein and RNA enzymes. We combined these properties with enzymatic recycling cleavage strategy to build a sensor which produced enhanced fluorescence signal. Sensitive and selective detection of GTP was successfully realized with the well-designed deoxyribozyme-based sensing platform by taking advantage of the self-phosphorylating ability of the kinase deoxyribozyme, efficient digestion capacity of λ exonuclease, and enzymatic recycling amplification of nicking enzyme. The method not only provides a platform for detecting GTP but also shows great potential in analyzing a variety of targets by combining deoxyribozymes with signal amplification strategy.
机译:通过体外选择鉴定出的自磷酸化脱氧核酶可以利用磷酸盐供体鸟苷5'-三磷酸(GTP)催化其自身的磷酸化,该物质在大多数细胞过程中起着至关重要的作用。基于自身磷酸化脱氧核酶的独特性质,我们报道了一种新型GTP传感器,结合λ核酸外切酶裂解反应和切口酶辅助的荧光信号放大过程。与蛋白质和RNA酶相比,具有特殊催化和结构特征的脱氧核酶显示出良好的稳定性。我们将这些特性与酶循环裂解策略相结合,构建了一种能够增强荧光信号的传感器。利用精心设计的基于脱氧核糖酶的传感平台,通过利用激酶脱氧核糖酶的自我磷酸化能力,λ外切核酸酶的有效消化能力以及切口酶的酶循环扩增,成功地实现了GTP的灵敏和选择性检测。该方法不仅提供了检测GTP的平台,而且通过结合脱氧核酶和信号放大策略在分析各种靶标方面显示出巨大的潜力。

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