Department of Mechanical Engineering, Johns Hopkins University, Baltimore, MD, 21218, USA.
Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA.
Adv Mater. 2021 Feb;33(7):e2005133. doi: 10.1002/adma.202005133. Epub 2021 Jan 18.
Plasmonic nanocavities are highly desirable for optical sensing because of their singular ability to confine light into deep subwavelength volumes. Yet, it remains profoundly challenging to fabricate structurally resilient nanocavities with high fidelity, and to obtain direct, noninvasive visualization of the plasmonic hotspots within such constructs. Herein, highly precise and robust nanocavities, entitled DNA-silicified template for Raman optical beacon (DNA-STROBE), are engineered by using silicified DNA scaffolds for spatial organization of discrete plasmonic nanoparticles. In addition to substantially enhancing structural stability and chemical inertness, DNA silicification significantly improves nanogap control, resulting simultaneously in large and controlled local electromagnetic field enhancement. The ultrasmall mode volume of the DNA-STROBE constructs promotes single-molecule occupancy enabling surface-enhanced Raman spectroscopy (SERS) observations of single-molecule activity even at elevated background concentration, significantly relaxing the restrictive pico- to nanomolar molecular concentration condition typically required for such investigations. Additionally, leveraging super-resolution SERS measurements allows noninvasive and diffraction-unlimited spatial profiling of otherwise unresolvable plasmonic hotspots. The highly programmable and reproducible nature of the DNA-STROBE, coupled with its quantitative label-free molecular readouts, provides a versatile platform with applications across the spectrum of nanophotonics and biomedical sciences.
等离子体纳米腔因其将光限制在深亚波长体积的独特能力而在光学传感中非常理想。然而,制造具有高保真度的结构弹性纳米腔,并获得此类结构中等离子体热点的直接、非侵入式可视化仍然极具挑战性。在此,通过使用硅化 DNA 支架来对离散等离子体纳米颗粒进行空间组织,设计出了高度精确和稳健的纳米腔,命名为 DNA-硅化模板用于喇曼光学信标 (DNA-STROBE)。除了显著提高结构稳定性和化学惰性外,DNA 硅化还显著改善了纳米间隙控制,从而同时实现了大的和受控的局部电磁场增强。DNA-STROBE 结构的超小模式体积促进了单分子占据,使得即使在背景浓度升高的情况下,也能够进行单分子活性的表面增强拉曼光谱 (SERS) 观察,这显著放宽了通常用于此类研究的皮摩尔至纳摩尔分子浓度条件的限制。此外,利用超分辨率 SERS 测量可以对原本不可分辨的等离子体热点进行非侵入式和无衍射限制的空间剖析。DNA-STROBE 的高度可编程和可重现性,加上其定量无标记分子读出,为跨越纳米光子学和生物医学科学光谱的应用提供了一个多功能平台。