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Gold nanocluster-DNase 1 hybrid materials for DNA contamination sensing

机译:金纳米簇-DNase 1杂合材料,用于DNA污染检测

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Protein encapsulated gold nanocluster (P-AuNC) synthesis was first demonstrated in 2009.[1] Initially these P-AuNCs were used as cellular imaging agents as the protein shell surrounding the AuNC made them highly biocompatible. However, recent studies have begun to show that these stabilizing proteins may also retain native biological function thus giving a dual functionality to these hybrid molecules. Here we present the synthesis of DNase 1 stabilized gold nanoclusters (DNase 1:AuNCs) with core sizes consisting either 8 or 25 atoms. The DNase 1:Au8NCs exhibit blue fluorescence whereas the DNase 1:AuNCs are red emitting. Moreover, in addition to the intense fluorescence emission; the synthesized DNase 1:AuNC hybrid retain the native functionality of the protein, allowing simultaneous detection and digestion of DNA with a detection limit of 2 μg/mL (Scheme 1). The DNase 1:AuNCs could be conveniently employed as efficient and fast sensors to augment the current inefficient and time consuming DNA contamination analysis techniques.
机译:蛋白质包封的金纳米簇(P-AuNC)的合成在2009年得到首次证明。[1]最初,这些P-AuNCs被用作细胞显像剂,因为AuNC周围的蛋白质外壳使它们具有高度的生物相容性。然而,最近的研究已经开始显示这些稳定蛋白也可以保留天然的生物学功能,从而使这些杂合分子具有双重功能。在这里,我们介绍了核酶大小为8或25个原子的DNase 1稳定金纳米簇(DNase 1:AuNCs)的合成。 DNase 1:Au8NCs发出蓝色荧光,而DNase 1:AuNCs发出红色荧光。而且,除了强烈的荧光发射外;合成的DNase 1:AuNC杂种保留了蛋白质的天然功能,允许同时检测和消化DNA,检测限为2μg/ mL(方案1)。 DNase 1:AuNCs可以方便地用作高效,快速的传感器,以增强当前效率低下且耗时的DNA污染分析技术。

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