Department of Biological Engineering, Inha University, Incheon 22212, Korea.
Nanoscale. 2018 Jul 5;10(25):11955-11961. doi: 10.1039/c8nr03168a.
A versatile nanopore sensing platform to detect any aptamer using nanopores by designing DNA hairpins that are complementary to the aptamer is described. This platform can detect the presence of aptamer binding targets regardless of their size, which has been a major hurdle for nanopore detection systems. Moreover, the signal-to-noise ratio is increased by eliminating most of the unwanted substances from the sample via simple sample preparation steps. To detect Bacillus thuringiensis HD-73 spores using this sensing platform, DNA hairpins complementary to the target-specific aptamers were designed, and the hairpins were characterized using alpha-hemolysin nanopores after the reaction of spores and aptamers and subsequent reaction with the complementary DNA hairpins. The platform exhibited a detection limit as low as 1.2 × 101 CFU mL-1 and was compatible with a wide range of spore concentrations from 1.2 × 101 CFU mL-1 to 1.2 × 106 CFU mL-1 while it is still expandable to higher spore concentrations.
一种通用的纳米孔传感平台,用于通过设计与适体互补的 DNA 发夹来检测任何适体的纳米孔。该平台可以检测到适体结合靶标的存在,而不受其大小的限制,这一直是纳米孔检测系统的主要障碍。此外,通过简单的样品制备步骤,可以从样品中去除大多数不需要的物质,从而提高信号与噪声的比值。为了使用这种传感平台检测苏云金芽孢杆菌 HD-73 孢子,设计了与靶标特异性适体互补的 DNA 发夹,并且在孢子和适体反应以及随后与互补 DNA 发夹反应后,使用α-溶血素纳米孔对发夹进行了表征。该平台的检测限低至 1.2×101 CFU mL-1,与 1.2×101 CFU mL-1 至 1.2×106 CFU mL-1 范围内的各种孢子浓度兼容,同时还可以扩展到更高的孢子浓度。