The Rowland Institute at Harvard, Harvard University, Cambridge, Massachusetts 02142, USA.
Nature. 2009 Dec 24;462(7276):1075-8. doi: 10.1038/nature08626. Epub 2009 Dec 13.
Techniques to detect and quantify DNA and RNA molecules in biological samples have had a central role in genomics research. Over the past decade, several techniques have been developed to improve detection performance and reduce the cost of genetic analysis. In particular, significant advances in label-free methods have been reported. Yet detection of DNA molecules at concentrations below the femtomolar level requires amplified detection schemes. Here we report a unique nanomechanical response of hybridized DNA and RNA molecules that serves as an intrinsic molecular label. Nanomechanical measurements on a microarray surface have sufficient background signal rejection to allow direct detection and counting of hybridized molecules. The digital response of the sensor provides a large dynamic range that is critical for gene expression profiling. We have measured differential expressions of microRNAs in tumour samples; such measurements have been shown to help discriminate between the tissue origins of metastatic tumours. Two hundred picograms of total RNA is found to be sufficient for this analysis. In addition, the limit of detection in pure samples is found to be one attomolar. These results suggest that nanomechanical read-out of microarrays promises attomolar-level sensitivity and large dynamic range for the analysis of gene expression, while eliminating biochemical manipulations, amplification and labelling.
在基因组学研究中,用于检测和定量生物样本中 DNA 和 RNA 分子的技术一直起着核心作用。在过去的十年中,已经开发出了几种技术来提高检测性能和降低基因分析成本。特别是,已经报道了在无标记方法方面的重大进展。然而,要在纳摩尔以下的浓度检测 DNA 分子,则需要放大检测方案。在这里,我们报告了杂交 DNA 和 RNA 分子的独特纳米力学响应,它可作为内在的分子标记。在微阵列表面上进行的纳米力学测量具有足够的背景信号抑制能力,可允许对杂交分子进行直接检测和计数。传感器的数字响应提供了一个关键的动态范围,这对于基因表达谱分析至关重要。我们已经测量了肿瘤样本中的 microRNA 的差异表达;这种测量被证明有助于区分转移性肿瘤的组织起源。发现 200 皮克的总 RNA 就足以进行这种分析。此外,在纯样品中的检测限被发现为 1 飞摩尔。这些结果表明,微阵列的纳米力学读出有望在分析基因表达时实现纳摩尔级的灵敏度和大动态范围,同时消除生化操作、放大和标记。