Molecular Recognition Research Center, Korea Institute of Science and Technology, Seoul 136-791, Republic of Korea.
J Chromatogr A. 2013 Nov 8;1315:195-9. doi: 10.1016/j.chroma.2013.09.048. Epub 2013 Sep 19.
MicroRNAs (miRNAs) are small, endogenous, single-stranded, noncoding RNAs. Circulating miRNAs are being considered as promising disease biomarkers. Indeed, single miRNAs have been associated with a wide variety of disease conditions and can target multiple mRNAs; therefore, several miRNAs may be simultaneously involved in disease progression and development. In this study, we developed a capillary electrophoresis with dual laser-induced fluorescence (CE with dual LIF) method using two color laser excitations for simultaneous determination of multiple miRNAs. Target miRNAs were hybridized with 6-FAM- or Cy5-labeled DNA probes for simultaneous determination of multiple miRNAs at excitation wavelengths of 488 and 635 nm. The hybridized miRNAs were separated using CE with dual LIF and detected within 13 min at excitation wavelengths of 488 and 635 nm without any interference or crosstalk. Additionally, the proposed approach was used successfully to detect and evaluate levels of several endogenous miRNAs from lung cancer cell lines. These results showed the potential of CE with dual LIF for fast, specific, simultaneous analysis of multiple miRNAs in cell extracts, biofluids, and tissues.
微 RNA(miRNAs)是小的、内源性的、单链的、非编码 RNA。循环 miRNA 被认为是有前途的疾病生物标志物。事实上,单一的 miRNA 与多种疾病状况有关,并且可以靶向多个 mRNA;因此,几种 miRNA 可能同时参与疾病的进展和发展。在这项研究中,我们开发了一种使用双激光激发的毛细管电泳与双激光诱导荧光(CE with dual LIF)方法,用于同时测定多种 miRNA。靶 miRNA 与 6-FAM 或 Cy5 标记的 DNA 探针杂交,用于在 488nm 和 635nm 的激发波长下同时测定多种 miRNA。使用 CE with dual LIF 分离杂交的 miRNA,并在没有任何干扰或串扰的情况下在 488nm 和 635nm 的激发波长下在 13 分钟内进行检测。此外,该方法还成功地用于检测和评估肺癌细胞系中几种内源性 miRNA 的水平。这些结果表明,CE with dual LIF 具有用于快速、特异性、同时分析细胞提取物、生物流体和组织中多种 miRNA 的潜力。