Institute of Photonics and Electronics, Academy of Sciences of the Czech Republic, Chaberská 57, 18251 Prague, Czech Republic.
Anal Chem. 2010 Dec 15;82(24):10110-5. doi: 10.1021/ac102131s. Epub 2010 Nov 19.
Microribonucleic acids (miRNAs) have been linked with various regulatory functions and disorders, such as cancers and heart diseases. They, therefore, present an important target for detection technologies for future medical diagnostics. We report here a novel method for rapid and sensitive miRNA detection and quantitation using surface plasmon resonance (SPR) sensor technology and a DNARNA antibody-based assay. The approach takes advantage of a novel high-performance portable SPR sensor instrument for spectroscopy of surface plasmons based on a special diffraction grating called a surface plasmon coupler and disperser (SPRCD). The surface of the grating is functionalized with thiolated DNA oligonucleotides which specifically capture miRNA from a liquid sample without amplification. Subsequently, an antibody that recognizes DNARNA hybrids is introduced to bind to the DNA*RNA complex and enhance sensor response to the captured miRNA. This approach allows detection of miRNA in less than 30 min at concentrations down to 2 pM with an absolute amount at high attomoles. The methodology is evaluated for analysis of miRNA from mouse liver tissues and is found to yield results which agree well with those provided by the quantitative polymerase chain reaction (qPCR).
微小 RNA(miRNAs)与各种调节功能和疾病有关,如癌症和心脏病。因此,它们为未来医学诊断的检测技术提供了一个重要的目标。我们在这里报告了一种使用表面等离子体共振(SPR)传感器技术和基于 DNARNA 抗体的测定法进行快速和敏感的 miRNA 检测和定量的新方法。该方法利用了一种新型的高性能便携式 SPR 传感器仪器,用于基于称为表面等离子体耦合器和分散器(SPRCD)的特殊衍射光栅的表面等离子体的光谱学。光栅的表面用硫醇化的 DNA 寡核苷酸功能化,该寡核苷酸可以特异性地从液体样品中捕获 miRNA,而无需扩增。随后,引入一种识别 DNARNA 杂交体的抗体以与 DNA*RNA 复合物结合,并增强传感器对捕获的 miRNA 的响应。这种方法允许在不到 30 分钟的时间内以低至 2 pM 的浓度进行 miRNA 的检测,并且绝对量达到高 attomoles。该方法学用于分析来自小鼠肝脏组织的 miRNA,并发现其结果与定量聚合酶链反应(qPCR)提供的结果非常吻合。