Department of Pharmacology, Jinling Hospital, Medical School of Nanjing University, Nanjing 210002, China.
Huadong Research Institute for Medicine and Biotechnics, Nanjing 210002, China.
Biosens Bioelectron. 2015 Apr 15;66:50-4. doi: 10.1016/j.bios.2014.10.077. Epub 2014 Nov 6.
Colorimetric DNA detection is preferable to methods in clinical molecular diagnostics, because no expensive equipment is required. Although many gold nanoparticle-based colorimetric DNA detection strategies have been developed to analyze DNA sequences of interest, few of them can detect somatic mutations due to their insufficient specificity. In this study, we proposed a colorimetric DNA detection method by coupling invasive reaction with nicking endonuclease-assisted nanoparticles amplification (IR-NEANA). A target DNA firstly produces many flaps by invasive reaction. Then the flaps are converted to targets of nicking reaction-assisted nanoparticles amplification by ligation reaction to produce the color change of AuNPs, which can be observed by naked eyes. The detection limit of IR-NEANA was determined as 1pM. Most importantly, the specificity of the method is high enough to pick up as low as 1% mutant from a large amount of wild-type DNA backgrounds. The EGFR gene mutated at c.2573 T>G in 9 tissue samples from non-small cell lung cancer patients were successfully detected by using IR-NEANA, suggesting that our proposed method can be used to detect somatic mutations in biological samples.
比色 DNA 检测优于临床分子诊断方法,因为它不需要昂贵的设备。尽管已经开发了许多基于金纳米粒子的比色 DNA 检测策略来分析感兴趣的 DNA 序列,但由于其特异性不足,很少有策略能够检测体细胞突变。在本研究中,我们提出了一种通过将侵入反应与缺口内切酶辅助的纳米粒子扩增(IR-NEANA)相结合的比色 DNA 检测方法。靶 DNA 首先通过侵入反应产生许多瓣。然后通过连接反应将瓣转化为缺口反应辅助的纳米粒子扩增的靶标,从而产生 AuNPs 的颜色变化,可通过肉眼观察到。IR-NEANA 的检测限为 1pM。最重要的是,该方法的特异性足够高,可以从大量野生型 DNA 背景中检测到低至 1%的突变体。通过使用 IR-NEANA,成功检测了来自非小细胞肺癌患者的 9 个组织样本中 EGFR 基因 c.2573 T>G 的突变,表明我们提出的方法可用于检测生物样本中的体细胞突变。