Department of Biochemistry, Yeungnam University, 280 Daehak-ro, Gyeongsan-si, Gyeongsangbuk-do, 38541, Republic of Korea.
Mikrochim Acta. 2021 Dec 23;189(1):34. doi: 10.1007/s00604-021-05138-9.
DNA is recognized as a powerful biomarker for clinical diagnostics because its specific sequences are closely related to the cause and development of diseases. However, achieving rapid, low-cost, and sensitive detection of short-length target DNA still remains a considerable challenge. Herein, we successfully combine the catalytic hairpin assembly (CHA) technique with capillary action to develop a new and cost-effective method, a target DNA- and pH-responsive DNA hydrogel-based capillary assay, for the naked eye detection of 24 nt short single-stranded target DNA. Upon contact of target DNA, three individual hairpin DNAs hybridize with each other to sufficiently amplify Y-shaped DNA nanostructures (Y-DNA) until they are completely consumed via CHA cycling reactions. Each arm of the resultant Y-DNA contains sticky ends with i-motif DNA structure-forming sequences that can be self-assembled in an acidic environment (pH 5.0) to form target DNA- and pH-responsive DNA hydrogels by means of i-motif DNA-driven crosslinking. When inserting a capillary tube in the resultant solution, the liquid level inside clearly reduces due to the decrease in capillary force induced by the gels. In this way, the developed assay demonstrates sensitive and quantitative detection, with a detection limit of approximately 10 pM of 24 nt short complementary DNA (cDNA) targeting SARS-CoV-2 RNA genes at room temperature within 1 h. The assay is further shown to successfully detect target cDNA in serum, and it is also applied to detect several types of target sequences. Requiring no analytic equipment, precise temperature control, or enzymatic reactions, the developed DNA hydrogel-based capillary assay has potential as a promising naked eye detection platform for target DNA in resource-limited clinical settings.
DNA 被认为是临床诊断的有力生物标志物,因为其特定序列与疾病的发生和发展密切相关。然而,实现短长度靶 DNA 的快速、低成本和灵敏检测仍然是一个相当大的挑战。在此,我们成功地将催化发夹组装(CHA)技术与毛细作用相结合,开发了一种新的、具有成本效益的方法,即基于靶 DNA 和 pH 响应的 DNA 水凝胶的毛细管检测法,用于裸眼检测 24 nt 短单链靶 DNA。当与靶 DNA 接触时,三个单独的发夹 DNA 彼此杂交,以充分扩增 Y 型 DNA 纳米结构(Y-DNA),直到它们通过 CHA 循环反应完全消耗。所得 Y-DNA 的每个臂都含有粘性末端,带有 i-motif DNA 结构形成序列,在酸性环境(pH 5.0)中可以自组装,通过 i-motif DNA 驱动的交联形成靶 DNA 和 pH 响应的 DNA 水凝胶。当将毛细管管插入所得溶液中时,由于凝胶引起的毛细作用力降低,内部的液位明显降低。通过这种方式,开发的检测方法具有敏感和定量检测的能力,在室温下,对靶向 SARS-CoV-2 RNA 基因的 24 nt 短互补 DNA(cDNA)的检测限约为 10 pM,检测时间为 1 小时。该检测方法还被证明可以成功地在血清中检测到靶 cDNA,并且还可以应用于检测几种类型的靶序列。该基于 DNA 水凝胶的毛细管检测法不需要分析设备、精确的温度控制或酶反应,具有作为在资源有限的临床环境中用于靶 DNA 的有前途的裸眼检测平台的潜力。