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首页> 外文期刊>Chemistry - A European Journal >Multiplex Detection of Endonucleases by Using a Multicolor Gold Nanobeacon
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Multiplex Detection of Endonucleases by Using a Multicolor Gold Nanobeacon

机译:使用多色金纳米信标多重检测内切核酸酶

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A highly sensitive and selective assay based on a novel enzyme-responsive multicolor gold nanobeacon has been developed for the multiplex detection of endonucleases, a group of very important nucleases. The nanobeacon takes advantage of the high specificity of DNA cleavage reactions combined with the unique fluorescence-quenching property of gold nanoparticles (AuNPs). To prepare the nanobeacon, three hairpin DNA reporters, each labeled at the 5′ terminus with a fluorescent dye (i.e., fluorescein amidite (FAM), carboxy-X-rhodamine (ROX), cyanine dye (Cy5)), that respond to one of three different endonucleases are co-assembled at the surface of AuNPs (15 nm). This assembly brings the dyes into very close proximity with the AuNP, which leads to significant quenching of the fluorescence due to the nanosurface energy-transfer (NSET) effect. When the nanobeacon is exposed to the targeted endonucleases, specific DNA cleavage occurs and pieces of DNA fragments are released from the AuNP surface along with the fluorescent dye, which results in the fluorescence recovery that provides the basis for a quantitative measurement of endonuclease activity. Three endonucleases, namely HaeIII, EcoRI, and EcoRV, were studied as the proof-of-concept analytes. These endonucleases in homogeneous mixture solutions were simultaneously quantified by the proposed assay with high sensitivity and specificity. The limits of detection obtained were in the range of 5.0×10−4 U mL−1 to 1.0×10−3 U mL−1 of endonuclease; these limits are at least 100 times more sensitive than the previously reported endonuclease assays. Endonuclease inhibitors impair the DNA cleavage, so it is anticipated that the present method has great potential for screening inhibitors of endonucleases. To demonstrate this application, the inhibitory effects of certain anticancer drugs on HaeIII, EcoRI, and EcoRV activities were studied. The present protocol proved to be sensitive, reliable, and easy to carry out.
机译:已经开发了一种基于新型酶反应性多色金纳米信标的高度灵敏和选择性的测定方法,用于多重检测内切核酸酶(一组非常重要的核酸酶)。纳米信标利用了DNA裂解反应的高特异性以及金纳米颗粒(AuNPs)独特的荧光猝灭特性。为了制备纳米信标,需要三个发夹DNA报道分子,每个在5'末端标记有荧光染料(即,荧光素亚酰胺(FAM),羧基-X-罗丹明(ROX),花青染料(Cy5))在AuNPs(15asenm)的表面共组装了三种不同的核酸内切酶。这种组装使染料与AuNP非常接近,由于纳米表面能量转移(NSET)效应,导致荧光显着猝灭。当纳米信标暴露于目标核酸内切酶时,发生特定的DNA切割,DNA片段与荧光染料一起从AuNP表面释放,这导致荧光回收,为定量测定核酸内切酶活性提供了基础。研究了三种核酸内切酶,即HaeIII,EcoRI和EcoRV,作为概念验证的分析物。通过提出的测定法同时定量均相混合溶液中的这些核酸内切酶,具有很高的灵敏度和特异性。获得的检出限在5.0×10 -4 U mL -1 到1.0×10 -3 U mL -1 ;这些限制的灵敏度至少比以前报道的核酸内切酶测定高100倍。核酸内切酶抑制剂损害DNA切割,因此预期本方法具有筛选核酸内切酶抑制剂的巨大潜力。为了证明该应用,研究了某些抗癌药物对HaeIII,EcoRI和EcoRV活性的抑制作用。本协议被证明是敏感,可靠并且易于执行的。

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