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Universal Ratiometric Photoelectrochemical Bioassay with Target-Nucleotide Transduction-Amplification and Electron-Transfer Tunneling Distance Regulation Strategies for Ultrasensitive Determination of microRNA in Cells

机译:具有靶核苷酸转导的通用比例光电化学生物测定和电子转移隧道距离调节细胞微小瘤超细瘤测定

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摘要

A universal ratiometric photoelectrochemical (PEC) bioassay, which could be readily expanded for ultrasensitive determination of various targets in complex biological matrixes, was established by coupling a target-nucleotide transduction-amplification with DNA nanomachine mediated electron-transfer tunneling distance regulation strategies. With the help of target nucleotide transduction-amplification strategy, the one input target signal could be transducted to corresponding multiple output DNA signals by nucleotide specific recognition technology, simultaneously leading to an efficient signal amplification for target. Then the output DNA could initiate the formation of four-way junction DNA nanomachine through binding-induced combination, by which the electron-transfer tunneling distance between photoactive materials and sensing interface could be regulated, simultaneously resulting an enhanced photocurrent signal from SiO2@methylene blue (SiO2@MB) as wavelength selective photoactive material in close proximity to sensing interface and a reduced photocurrent signal from another wavelength selective photoactive, material CdS quantum dots (CdS QDs) away from sensing interface for photocurrent signal ratio calculation. Using microRNA-141 (miRNA-141) as target model, the constructed biosensor demonstrated favorable accuracy and excellent sensitivity down to the femtomolar level. Impressively, the proposed assay overcame the heavy dependence of target on photoactive materials in current ratiometric PEC assay and demonstrated admirably universal applicability for determination of various targets such as metal ions, miRNAs, DNAs, and proteins by merely two different photoactive materials (SiO2@MB and CdS QDs), paving the way to application of universal ratiometric PEC assay in environmental tests, clinical diagnosis, and other related subjects.
机译:通过偶联具有DNA纳米机介导的电子转移隧道距离调节策略的靶核苷酸转导扩增,建立了可以容易地扩增用于超细生物学基质中各种靶标的各种靶标的不同靶标的通用的比率光电化学(PEC)生物测定。借助于靶核苷酸转导扩增策略,可以通过核苷酸特异性识别技术转换为对应的多输出DNA信号,同时导致目标的有效信号放大。然后,输出DNA可以通过结合诱导的组合开始形成四通路连接DNA纳米机,通过该组合可以调节光活性材料和传感界面之间的电子转移隧道距离,同时产生来自SiO 2的增强的光电流信号@亚甲基蓝色(SiO2 @ MB)作为波长选择性的光活性物质,其靠近感测界面和来自另一波长选择性光电动物的减小的光电流信号,材料CDS量子点(CDS QD)远离感测光电流信号比计算。使用MicroRNA-141(miRNA-141)作为靶模型,构造的生物传感器展示了良好的准确性和低于毫微微摩尔水平的敏感性。令人印象深刻地,所提出的测定克服了靶标在当前比例PEC测定中的光活性物质的重依赖性,并通过仅两种不同的光活性物质(SiO 2 @ MB,令人钦佩地普遍适用于测定金属离子,miRNA,DNA和蛋白质等各种靶标(SiO 2 @ MB和CDS QDS),铺平了在环境试验,临床诊断和其他相关科目中应用通用比率PEC测定的方式。

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  • 来源
    《Analytical chemistry》 |2017年第17期|共7页
  • 作者单位

    Southwest Univ Coll Chem &

    Chem Engn Key Lab Luminescent &

    Real Time Analyt Chem Minist Educ Chongqing 400715 Peoples R China;

    Southwest Univ Coll Chem &

    Chem Engn Key Lab Luminescent &

    Real Time Analyt Chem Minist Educ Chongqing 400715 Peoples R China;

    Southwest Univ Coll Chem &

    Chem Engn Key Lab Luminescent &

    Real Time Analyt Chem Minist Educ Chongqing 400715 Peoples R China;

    Southwest Univ Coll Chem &

    Chem Engn Key Lab Luminescent &

    Real Time Analyt Chem Minist Educ Chongqing 400715 Peoples R China;

    Southwest Univ Coll Chem &

    Chem Engn Key Lab Luminescent &

    Real Time Analyt Chem Minist Educ Chongqing 400715 Peoples R China;

    Southwest Univ Coll Chem &

    Chem Engn Key Lab Luminescent &

    Real Time Analyt Chem Minist Educ Chongqing 400715 Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分析化学;
  • 关键词

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