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 versatile biosensing system for DNA-related enzyme activity assay via the synthesis of silver nanoclusters using enzymatically-generated DNA as template
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A versatile biosensing system for DNA-related enzyme activity assay via the synthesis of silver nanoclusters using enzymatically-generated DNA as template

机译:一种多功能的生物传感系统,用于通过使用酶促生成的DNA作为模板的银纳米团簇的合成来进行DNA相关的酶活性测定

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In the present day, oligonucleotide-encapsulated silver clusters (DNA-AgNCs) have been widely applied into bio-analysis as a signal producer. Herein, we developed a novel method to synthesize DNA-AgNCs encapsulated by long-chain cytosine (C)-rich DNA. Such DNA was polymerized in a template-free way by terminal deoxynucleotidyl transferase (TdT). We demonstrated that TdT-polymerized long chain C-rich DNA can serve as an excellent template for AgNCs synthesis. Based on this novel synthesis strategy, we developed a label-free and turn-on fluorescence assay to detect TdT activity with ultralow limit of detection (LOD) of 0.0318 U and ultrahigh signal to background (S/B) of 46.7. Furthermore, our proposed method was extended to a versatile biosensing strategy for turn-on nucleases activity assay based on the enzyme-activated TdT polymerization. Two nucleases, EcoRI and ExoIII as model of endonuclease and exonuclease, respectively, have been detected with high selectivity and competitive low LOD of 0.0629 U and 0.00867 U, respectively. Our work demonstrates the feasibility of TdT polymerization-based DNA- AgNCs synthesis strategy as a versatile and potent biosensing platform to detect the activity of DNA- related enzymes.
机译:如今,寡核苷酸包封的银簇(DNA-AgNCs)已作为信号产生剂被广泛应用于生物分析。在这里,我们开发了一种新颖的方法来合成由富含长链胞嘧啶(C)的DNA包裹的DNA-AgNCs。这样的DNA通过末端脱氧核苷酸转移酶(TdT)以无模板的方式聚合。我们证明了TdT聚合的长链富含C的DNA可以作为AgNCs合成的出色模板。基于这种新颖的合成策略,我们开发了一种无标记的开启荧光测定法来检测TdT活性,其超低检测限(LOD)为0.0318 U,超高背景信号(S / B)为46.7。此外,我们提出的方法已扩展到基于酶激活的TdT聚合的核酸酶活性测定的通用生物传感策略。已检测到两种核酸酶,分别为EcoRI和ExoIII,分别作为内切核酸酶和核酸外切酶的模型,具有高选择性和竞争性低LOD,分别为0.0629 U和0.00867U。我们的工作证明了基于TdT聚合的DNA-AgNCs合成策略作为检测DNA相关酶活性的通用且有效的生物传感平台的可行性。

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