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利用 Poly-Guanine-介导的原位合成构建多价 DNA 功能化各向异性金纳米粒子用于基于 LSPR 的分析:以 OncomiR-155 为例

Building Polyvalent DNA-Functionalized Anisotropic AuNPs using Poly-Guanine-Mediated In-Situ Synthesis for LSPR-Based Assays: Case Study on OncomiR-155.

机构信息

Department of Nanobiotechnology, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran.

Department of Biochemistry, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran.

出版信息

Photochem Photobiol. 2022 Sep;98(5):1043-1049. doi: 10.1111/php.13586. Epub 2022 Feb 1.

Abstract

DNA-functionalized gold nanoparticles (DNA-AuNPs) hold great promise for numerous biomedical applications, especially the building of well-defined nanosystems. Previously reported methods for the preparation of DNA-AuNPs all rely on the use of DNA-bearing free thiol or disulfide groups at their 3'/5' ends. But here we report a novel polyvalent DNA-AuNPs conjugation approach by in-situ fast synthesis of AuNPs at the polyguanine (G ) strands. As confirmed by both TEM images and gel electrophoresis analysis, many poly G strand can form an individual anisotropic AuNP and so each AuNP functionalized with a dense layer of DNA, resulting in the formation of polyvalent (p)DNA-AuNPs. The general applicability of this novel approach was further verified in hybridization test and UV-Vis spectroscopy results show that pDNA-AuNPs conjugation is more attractive in biomedical diagnosis and specific sequence detection like microRNA-155 by using an extra-strand poly G with "sticky end" that are complementary to the target sequence.

摘要

DNA 功能化金纳米粒子(DNA-AuNPs)在众多生物医学应用中具有广阔的应用前景,特别是在构建具有明确定义的纳米系统方面。以前报道的制备 DNA-AuNPs 的方法都依赖于在其 3'/5' 末端使用带有游离巯基或二硫键的 DNA。但在这里,我们通过在聚鸟嘌呤 (G) 链上原位快速合成 AuNPs,报道了一种新颖的多价 DNA-AuNPs 偶联方法。正如 TEM 图像和凝胶电泳分析所证实的那样,许多聚 G 链可以形成单个各向异性的 AuNP,因此每个 AuNP 都被一层密集的 DNA 功能化,从而形成多价 (p)DNA-AuNPs。该新方法的通用性在杂交试验中得到了进一步验证,UV-Vis 光谱结果表明,通过使用与靶序列互补的带有“粘性末端”的额外聚 G 链,pDNA-AuNPs 偶联在生物医学诊断和特定序列检测(如 microRNA-155)中更具吸引力。

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