Bio-X Institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Shanghai Jiao Tong University, Shanghai, China.
PLoS One. 2013 Aug 21;8(8):e69856. doi: 10.1371/journal.pone.0069856. eCollection 2013.
DNA origami is an emerging technology that assembles hundreds of staple strands and one single-strand DNA into certain nanopattern. It has been widely used in various fields including detection of biological molecules such as DNA, RNA and proteins. MicroRNAs (miRNAs) play important roles in post-transcriptional gene repression as well as many other biological processes such as cell growth and differentiation. Alterations of miRNAs' expression contribute to many human diseases. However, it is still a challenge to quantitatively detect miRNAs by origami technology. In this study, we developed a novel approach based on streptavidin and quantum dots binding complex (STV-QDs) labeled single strand displacement reaction on DNA origami to quantitatively detect the concentration of miRNAs. We illustrated a linear relationship between the concentration of an exemplary miRNA as miRNA-133 and the STV-QDs hybridization efficiency; the results demonstrated that it is an accurate nano-scale miRNA quantifier motif. In addition, both symmetrical rectangular motif and asymmetrical China-map motif were tested. With significant linearity in both motifs, our experiments suggested that DNA Origami motif with arbitrary shape can be utilized in this method. Since this DNA origami-based method we developed owns the unique advantages of simple, time-and-material-saving, potentially multi-targets testing in one motif and relatively accurate for certain impurity samples as counted directly by atomic force microscopy rather than fluorescence signal detection, it may be widely used in quantification of miRNAs.
DNA 折纸术是一种新兴的技术,它可以将数百个订书钉和一条单链 DNA 组装成特定的纳米图案。它已广泛应用于各个领域,包括检测生物分子如 DNA、RNA 和蛋白质。MicroRNAs(miRNAs)在转录后基因沉默以及细胞生长和分化等许多其他生物学过程中发挥重要作用。miRNAs 表达的改变与许多人类疾病有关。然而,通过折纸技术定量检测 miRNAs 仍然是一个挑战。在本研究中,我们开发了一种基于链霉亲和素和量子点结合复合物(STV-QDs)标记单链置换反应的新型方法,用于定量检测 miRNAs 的浓度。我们说明了示例性 miRNA(miRNA-133)的浓度与 STV-QDs 杂交效率之间的线性关系;结果表明,它是一种准确的纳米级 miRNA 定量分子。此外,还测试了对称矩形图案和不对称中国地图图案。在这两种图案中都具有显著的线性关系,我们的实验表明,具有任意形状的 DNA 折纸图案都可以应用于这种方法。由于我们开发的这种基于 DNA 折纸术的方法具有独特的优势,例如简单、省时省力、在一个图案中可以进行多靶点测试,并且对于某些杂质样品相对准确,因为可以直接通过原子力显微镜而不是荧光信号检测进行计数,因此它可能广泛应用于 miRNAs 的定量检测。