Program for Nanomedical Science and Technology, Yonsei University, Seoul, 120-749, Republic of Korea.
Biosens Bioelectron. 2012 Feb 15;32(1):141-7. doi: 10.1016/j.bios.2011.11.047. Epub 2011 Dec 6.
In this report, we have investigated enhanced surface plasmon resonance (SPR) detection of DNA hybridization using gold core - silica shell nanoparticles in localized plasmonic fields. The plasmonic fields were localized by periodic linear gratings. Experimental results measured for hybridization of 24-mer single-stranded DNA oligomers suggest that core-shell nanoparticles (CSNPs) on gratings of 400 nm period provide enhanced optical signatures by 36 times over conventional thin film-based SPR detection. CSNP-mediated DNA hybridization produced 3 times larger angular shift compared to gold nanoparticles of the same core size. We have also analyzed the effect of structural variation. The enhancement using CSNPs was associated with increased surface area and index contrast that is combined by improved plasmon coupling with localized fields on gratings. The combined approach for conjugated measurement of a biomolecular interaction on grating structures is expected to lower the limit of detection to the order of a few tens of fg/mm(2).
在本报告中,我们研究了利用金核- 硅壳纳米粒子在局域等离子体场中增强的 DNA 杂交表面等离子体共振(SPR)检测。等离子体场通过周期性线性光栅进行局域化。实验结果表明,对于 24 -mer 单链 DNA 寡聚物的杂交,400nm 周期光栅上的核壳纳米粒子(CSNP)提供了比传统基于薄膜 SPR 检测高 36 倍的光学特征。与相同核心尺寸的金纳米粒子相比,CSNP 介导的 DNA 杂交产生了 3 倍更大的角度位移。我们还分析了结构变化的影响。使用 CSNP 的增强与表面积和折射率对比度的增加有关,这是通过在光栅上与局域场的改进等离子体耦合来实现的。这种在光栅结构上共轭测量生物分子相互作用的组合方法有望将检测限降低到几十 fg/mm(2)的数量级。