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Design of a fluorescence aptaswitch based on the aptamer modulated nano-surface impact on the fluorescence particles

机译:基于适体调节纳米表面撞击对荧光颗粒的荧光Aptaswitch的设计

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摘要

The concept of DNA based stabilization of nanostructures to enhance the surface reactivity has been the focus of great interest in the design of colorimetric aptaswitches. Whereas, colorimetric methodologies have limited sensitivity, this concept is rarely considered for other sensing approaches such as those based on fluorescence detection. In this paper, we have investigated the impact of reversible assembly of a single strand DNA aptamer on nanoparticle surface chemistry, involving target tuneable electrostatic and steric repulsion phenomena for fluorescence based detection of molecular interactions. In the same context, literature reported fluorescence based aptamer assays are prone to certain limitations such as complicated labelling chemistry, low conjugation yield, low binding affinity and elevated cost per assay. Alternatively, our designed aptaswitch capitalizes on the surface chemistry of nanoparticles to quench the response of fluorescence particles, eliminating the need of bioconjugation with a fluorophore. As a proof of concept, the proposed methodology was used for the detection of ochratoxin A with TiO _(2) nanoparticles as a representative nanomaterial. We expect that this concept may pave a new way to probe aptamer-target binding events, since any nanomaterials with fluorescence quenching characteristics can be regulated in the same manner.
机译:基于DNA稳定的纳米结构的概念提高了表面反应性,是对比色APTaswitch的设计非常兴趣的焦点。然而,比色方法具有有限的灵敏度,这概念很少考虑其他感测方法,例如基于荧光检测的方法。在本文中,我们研究了可逆组装在纳米颗粒表面化学对纳米粒子表面化学的影响,涉及基于荧光的荧光检测的靶可调静电和空间排斥现象。在相同的情况下,文献报告的荧光基适体测定易于某些限制,例如复杂的标记化学,低缀合产率,低结合亲和力和每种测定的升高成本。或者,我们设计的Aptaswitch大写纳米颗粒的表面化学物质,以终止荧光颗粒的响应,从而消除了荧光团的生物缀合的需要。作为概念证明,所提出的方法用于检测与TiO _(2)纳米颗粒作为代表性纳米材料的核毒素A.我们期望该概念可以铺平探测适体靶结合事件的新方法,因为可以以相同的方式调节任何具有荧光猝灭特性的纳米材料。

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