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利用 DNA-金纳米粒子探针进行绝对和直接的 microRNA 定量分析。

Absolute and direct microRNA quantification using DNA-gold nanoparticle probes.

机构信息

Center for Biomolecular Nanotechnologies@UniLe, Istituto Italiano di Tecnologia (IIT) ,Via Barsanti, 73010 Arnesano, Lecce, Italy.

出版信息

J Am Chem Soc. 2014 Feb 12;136(6):2264-7. doi: 10.1021/ja412152x. Epub 2014 Feb 3.

Abstract

DNA-gold nanoparticle probes are implemented in a simple strategy for direct microRNA (miRNA) quantification. Fluorescently labeled DNA-probe strands are immobilized on PEGylated gold nanoparticles (AuNPs). In the presence of target miRNA, DNA-RNA heteroduplexes are formed and become substrate for the endonuclease DSN (duplex-specific nuclease). Enzymatic hydrolysis of the DNA strands yields a fluorescence signal due to diffusion of the fluorophores away from the gold surface. We show that the molecular design of our DNA-AuNP probes, with the DNA strands immobilized on top of the PEG-based passivation layer, results in nearly unaltered enzymatic activity toward immobilized heteroduplexes compared to substrates free in solution. The assay, developed in a real-time format, allows absolute quantification of as little as 0.2 fmol of miR-203. We also show the application of the assay for direct quantification of cancer-related miR-203 and miR-21 in samples of extracted total RNA from cell cultures. The possibility of direct and absolute quantification may significantly advance the use of microRNAs as biomarkers in the clinical praxis.

摘要

DNA-金纳米粒子探针被应用于一种简单的策略,用于直接定量检测 microRNA(miRNA)。荧光标记的 DNA 探针链被固定在聚乙二醇化的金纳米粒子(AuNPs)上。在靶 miRNA 的存在下,形成 DNA-RNA 异源双链体,并成为内切酶 DSN(双链特异性核酸内切酶)的底物。由于荧光团从金表面扩散,DNA 链的酶促水解产生荧光信号。我们表明,我们的 DNA-AuNP 探针的分子设计,其中 DNA 链固定在基于 PEG 的钝化层的顶部,与游离在溶液中的底物相比,对固定化异源双链体的酶活性几乎没有改变。该测定法以实时格式开发,允许对低至 0.2 fmol 的 miR-203 进行绝对定量。我们还展示了该测定法在直接定量检测细胞培养物中提取的总 RNA 样品中的癌症相关 miR-203 和 miR-21 的应用。直接和绝对定量的可能性可能会极大地推动 miRNA 作为临床实践中的生物标志物的应用。

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