Department of Materials Science & Engineering, Boise State University, Boise, ID 83725, United States.
Biosens Bioelectron. 2013 Dec 15;50:382-6. doi: 10.1016/j.bios.2013.06.063. Epub 2013 Jul 11.
A catalytic colorimetric detection scheme that incorporates a DNA-based hybridization chain reaction into gold nanoparticles was designed and tested. While direct aggregation forms an inter-particle linkage from only one target DNA strand, catalytic aggregation forms multiple linkages from a single target DNA strand. Gold nanoparticles were functionalized with thiol-modified DNA strands capable of undergoing hybridization chain reactions. The changes in their absorption spectra were measured at different times and target concentrations and compared against direct aggregation. Catalytic aggregation showed a multifold increase in sensitivity at low target concentrations when compared to direct aggregation. Gel electrophoresis was performed to compare DNA hybridization reactions in catalytic and direct aggregation schemes, and the product formation was confirmed in the catalytic aggregation scheme at low levels of target concentrations. The catalytic aggregation scheme also showed high target specificity. This application of a DNA reaction network to gold nanoparticle-based colorimetric detection enables highly-sensitive, field-deployable, colorimetric readout systems capable of detecting a variety of biomolecules.
设计并测试了一种将基于 DNA 的杂交链式反应纳入金纳米粒子的催化比色检测方案。直接聚集仅由一条靶 DNA 链形成粒子间连接,而催化聚集则由一条靶 DNA 链形成多个连接。金纳米粒子用经过巯基修饰的 DNA 链功能化,这些 DNA 链能够进行杂交链式反应。在不同时间和靶浓度下测量它们的吸收光谱变化,并与直接聚集进行比较。与直接聚集相比,催化聚集在低靶浓度下表现出灵敏度的多倍增加。进行凝胶电泳以比较催化和直接聚集方案中的 DNA 杂交反应,并在催化聚集方案中在低靶浓度水平下确认产物形成。催化聚集方案还表现出高的靶特异性。将 DNA 反应网络应用于基于金纳米粒子的比色检测中,能够实现高度灵敏、可现场部署、比色读出系统,能够检测多种生物分子。