College of Chemistry, Sichuan University, Chengdu 610064, P. R. China.
Anal Chem. 2020 Jul 7;92(13):8867-8873. doi: 10.1021/acs.analchem.0c00575. Epub 2020 Jun 8.
With the aim of detecting low frequency of drug resistant mutation T790M against wild-type sequences, we reported a two-dimensional signal analysis strategy by combining a three locked nucleic acids (LNAs)-modified probe (LP15-3t) and an α-HL nanopore. The specific hybridization of the LP15-3t probe with the T790M generated unique long two-level signals, including characteristic blocking current and characteristic dwell time. Due to the significant dwell time difference (114.2-fold) and the blocking current difference ranging from 81% to 96%, this two-dimensional signal analysis strategy can simultaneously distinguish T790M sequences with a sensitivity of 0.0001% against wild-type sequences. The LOD of T790M was 0.1 pM. This high discrimination capability would have great potential in the detection of rare mutation sequences and the early monitoring of clinical outcome of NSCLC patients with TKI drug resistance.
为了检测针对野生型序列的低频耐药突变 T790M,我们报道了一种二维信号分析策略,该策略结合了三个锁核酸(LNA)修饰的探针(LP15-3t)和一个α-HL 纳米孔。LP15-3t 探针与 T790M 的特异性杂交产生了独特的长两级信号,包括特征阻断电流和特征停留时间。由于显著的停留时间差异(114.2 倍)和阻断电流差异范围为 81%至 96%,这种二维信号分析策略可以同时以 0.0001%的灵敏度区分 T790M 序列和野生型序列。T790M 的 LOD 为 0.1 pM。这种高分辨能力在检测罕见突变序列和早期监测 NSCLC 患者 TKI 耐药的临床结果方面具有巨大潜力。