State Key Laboratory of Analytical Chemistry for Life Science and Collaborative Innovation Center of Chemistry for Life Science, School of Chemistry and Chemical Engineering , Nanjing University , Nanjing 210023 , China.
Department of Urology, Nanjing Drum Tower Hospital, Medical School of Nanjing University, Institute of Urology , Nanjing University , Nanjing 210008 , China.
Anal Chem. 2018 Oct 16;90(20):11892-11898. doi: 10.1021/acs.analchem.8b01966. Epub 2018 Sep 28.
Highly stable circulating microRNAs (miRNAs) are currently recognized as a novel potential biomarker for clinical cancer diagnosis in the early stage. However, limited by its low concentration, high sequence similarity, as well as the numerous interferences in body fluids, detection of miRNA in whole blood with sufficient selectivity and sensitivity is still challenging. Herein, we reported the integration of entropy-driven toehold-mediated DNA strand displacement (ETSD) reaction with magnetic beads (MB) toward the energy-transfer-based photoelectrochemical (PEC) detection of the prostate carcinoma (PCa) biomarker miRNA-141 in a real blood sample. In this protocol, the ETSD reaction was divided into two steps, and cooperated with magnetic separation, target extraction and amplification could be realized in a single test and ultrasensitive detection of miRNA-141 could be achieved in undiluted whole blood sample. This work proposed a new solution for sensitive biomolecular detection in a complex biological milieu and exhibited great promise for future clinical cancer diagnosis.
高度稳定的循环 microRNAs(miRNAs)目前被认为是一种新型的潜在生物标志物,可用于临床癌症的早期诊断。然而,由于 miRNA 在血液中的浓度低、序列相似性高以及体液中存在大量干扰,因此用足够的选择性和灵敏度来检测全血中的 miRNA 仍然具有挑战性。在此,我们报道了熵驱动引发的 DNA 链置换(ETSD)反应与磁珠(MB)的整合,用于基于能量转移的光电化学(PEC)检测前列腺癌(PCa)生物标志物 miRNA-141 在真实的血液样本中。在本方案中,将 ETSD 反应分为两步进行,通过磁分离,可在单次测试中实现目标提取和扩增,并可在未稀释的全血样本中实现对 miRNA-141 的超灵敏检测。这项工作为复杂生物环境中的敏感生物分子检测提出了一种新的解决方案,为未来的临床癌症诊断展示了广阔的前景。