School of Electrical and Electronic Engineering, Yonsei Institute of Medical Instruments Technology, Yonsei University, Seoul 120-749, Republic of Korea.
Biosens Bioelectron. 2014 Jan 15;51:401-7. doi: 10.1016/j.bios.2013.08.008. Epub 2013 Aug 17.
We report extremely sensitive plasmonic detection that was performed label-free based on the colocalization of target DNA molecules and electromagnetic hot spots excited at 3D nanogap arrays. The colocalization was self-aligned by oblique evaporation of a dielectric mask over the 3D nanopatterns, which creates nanogaps for spatially selective target binding. The feasibility was experimentally confirmed by measuring hybridization of 24-mer single-stranded DNA oligonucleotides on triangular and circular 3D nanogap arrays. We were able to achieve significantly amplified optical signatures that lead to sensitivity enhancement in terms of detectable binding capacity in reference to conventional thin film-based surface plasmon resonance detection on the order of 1 fg/mm(2).
我们报告了一种极其灵敏的等离子体检测方法,该方法基于目标 DNA 分子与在 3D 纳米缝隙阵列中激发的电磁热点的共定位,无需标记即可实现。通过在 3D 纳米图案上斜向蒸发介电掩模来实现共定位,该掩模会在纳米图案上产生纳米缝隙,用于空间选择性地结合目标物。实验通过测量三角形和圆形 3D 纳米缝隙阵列上 24 聚体单链 DNA 寡核苷酸的杂交,验证了这种方法的可行性。我们能够实现显著放大的光学信号,从而使检测能力得到增强,与传统的基于薄膜的表面等离子体共振检测相比,灵敏度提高了 1 fg/mm(2) 左右。