Shandong Provincial Key Laboratory of Detection Technology for Tumor Makers, College of Chemistry and Chemical Engineering, Linyi University , Linyi, Shandong 276005, P. R. China.
College of Chemistry and Material Science, Shandong Agricultural University , Taian, Shandong 271018, P. R. China.
Anal Chem. 2018 Jan 2;90(1):1029-1034. doi: 10.1021/acs.analchem.7b04584. Epub 2017 Dec 19.
Sensitive detection of cancer cells at extremely low concentrations would greatly facilitate the screening and early diagnosis of cancer. Herein, we present a novel nanopore-based strategy for ultrasensitive detection of Ramos cells (human Burkitt's lymphoma cells), by combining the enzymatic signal amplification with an aerolysin nanopore sensor. In this assay, an aptamer for Ramos cells was prehybridized with a short complementary DNA. The presence of target cells causes the target-aptamer complex to unwind to free the complementary DNA, which would subsequently trigger the enzymatic cycling amplification. This process eventually generated a large number of output DNA, which could quantitatively produce characteristic current events when translocated through aerolysin. The proposed method exhibits excellent sensitivity, and as few as 5 Ramos cells could be detected. With good selectivity, the approach can allow for the determination of cancer cells in human serum, offering a powerful tool for biomedical research and clinical diagnosis.
在极低浓度下灵敏地检测癌细胞将极大地促进癌症的筛查和早期诊断。在此,我们提出了一种基于纳米孔的新策略,通过将酶信号放大与溶菌酶纳米孔传感器相结合,用于超灵敏检测 Ramos 细胞(人伯基特淋巴瘤细胞)。在该测定中,Ramos 细胞的适体与短互补 DNA 预先杂交。靶细胞的存在导致靶-适体复合物解链以释放互补 DNA,随后触发酶循环扩增。这个过程最终产生了大量的输出 DNA,当它们穿过溶菌酶时可以定量产生特征电流事件。所提出的方法表现出优异的灵敏度,可检测到低至 5 个 Ramos 细胞。该方法具有良好的选择性,可用于测定人血清中的癌细胞,为生物医学研究和临床诊断提供了有力工具。