Center of Medical Physics and Technology, Hefei Institutes of Physical Science, Chinese Academy of Sciences, Hefei, Anhui 230031, China.
School of Life Science, Anhui University, Hefei, Anhui 230601, China.
Nucleic Acids Res. 2020 Mar 18;48(5):2220-2231. doi: 10.1093/nar/gkaa016.
Hybridization chain reaction (HCR) was a significant discovery for the development of nanoscale materials and devices. One key challenge for HCR is the vulnerability to background leakage in the absence of the initiator. Here, we systematically analyze the sources of leakage and refine leak-resistant rule by using molecular thermodynamics and dynamics, biochemical and biophysical methods. Transient melting of DNA hairpin is revealed to be the underlying cause of leakage and that this can be mitigated through careful consideration of the sequence thermodynamics. The transition threshold of the energy barrier is proposed as a testing benchmark of leak-resistance DNA hairpins. The universal design of DNA hairpins is illustrated by the analysis of hsa-miR-21-5p as biomarker when used in conjunction with surface-enhanced Raman spectroscopy. We further extend the strategy for specific signal amplification of miRNA homologs. Significantly, it possibly provides a practical route to improve the accuracy of DNA self-assembly for signal amplification, and that could facilitate the development of sensors for the sensitive detection of interest molecules in biotechnology and clinical medicine.
杂交链式反应(HCR)是纳米材料和器件发展的重大发现。HCR 的一个关键挑战是在没有引发剂的情况下容易受到背景泄漏的影响。在这里,我们使用分子热力学和动力学、生化和生物物理方法系统地分析了泄漏的来源,并通过仔细考虑序列热力学来改进抗泄漏规则。揭示了 DNA 发夹的瞬时熔化是泄漏的根本原因,通过仔细考虑序列热力学可以减轻这种情况。提出了能量势垒的跃迁阈值作为抗泄漏 DNA 发夹的测试基准。通过结合表面增强拉曼光谱分析 hsa-miR-21-5p 作为生物标志物,说明了 DNA 发夹的通用设计。我们进一步扩展了用于 miRNA 同源物的特定信号放大的策略。值得注意的是,它可能为提高 DNA 自组装信号放大的准确性提供了一条实用途径,从而有助于开发用于生物技术和临床医学中感兴趣分子的灵敏检测的传感器。