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首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >A TdT-mediated cascade signal amplification strategy based on dendritic DNA matrix for label-free multifunctional electrochemical biosensing
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A TdT-mediated cascade signal amplification strategy based on dendritic DNA matrix for label-free multifunctional electrochemical biosensing

机译:基于树突状DNA基质的TdT介导的级联信号放大策略,用于无标记的多功能电化学生物传感

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摘要

We describe a novel label-free amplified multifunctional strategy of dendritic electrochemical DNA sensor based on terminal deoxynucleotidyl transferase (TdT). We have found that the sequence composition of TdT-yielded DNA is largely dependent on the constitution of substrate deoxynucleotides (dNTPs) pool. After rational design of dNTPs pool and controllable TdT polymerization, dendritic protocol has been developed involving two-type amplification strategies; one is the formation of "trunk" and "branch" of the dendritic electrochemical sensor by TdT amplification; the other is the introduction of nucleic acid functionalized Au nanoparticles (DNA-AuNPs) for multiple branching. The results indicate that the G-rich ssDNA, which is synthesized under the condition of 40% deoxyadenosine triphosphate (dATP) and 60% deoxyguanosine triphosphate (dGTP), can be induced to form a long signal strand to G-quadruples (G4) in the presence of Pb2+. The electrochemical sensing platform is employed for sequence-specific DNA detection and the detection limit is as low as 1 fM. Our multifunctional strategy is further extended to Pb2+ detection and thrombin aptasensor. This proposed sensor displays excellent sensitivity and selectivity, and is applied for detection in complicated samples successfully. (C) 2014 Elsevier B.V. All rights reserved.
机译:我们描述了一种基于末端脱氧核苷酸转移酶(TdT)的树突状电化学DNA传感器的新型无标记扩增多功能策略。我们发现,TdT产生的DNA的序列组成在很大程度上取决于底物脱氧核苷酸(dNTPs)库的组成。在合理设计dNTPs库并控制TdT聚合后,已经开发出涉及两种扩增策略的树突方案。一种是通过TdT扩增形成树枝状电化学传感器的“主体”和“分支”。另一种是引入核酸功能化的金纳米颗粒(DNA-AuNPs)进行多分支。结果表明,在40%的脱氧腺苷三磷酸(dATP)和60%的脱氧鸟苷三磷酸(dGTP)的条件下合成的富含G的ssDNA可以形成长信号链到G-四联体(G4)。 Pb2 +的存在。电化学传感平台用于序列特异性DNA检测,检测限低至1 fM。我们的多功能策略进一步扩展到Pb2 +检测和凝血酶适体传感器。该传感器具有极好的灵敏度和选择性,可成功用于复杂样品的检测。 (C)2014 Elsevier B.V.保留所有权利。

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