Midelet Johanna, El-Sagheer Afaf H, Brown Tom, Kanaras Antonios G, Débarre Anne, Werts Martinus H V
Physics and Astronomy, University of Southampton, Southampton, SO17 1BJ, United Kingdom.
Department of Chemistry, University of Oxford, 12 Mansfield Road, Oxford, OX1 3TA, United Kingdom.
Chemphyschem. 2018 Apr 5;19(7):827-836. doi: 10.1002/cphc.201701228. Epub 2018 Feb 21.
Two-photon photoluminescence (TPPL) emission spectra of DNA-gold nanoparticle (AuNP) monoconjugates and the corresponding DNA-linked AuNP dimers are obtained by photon time-of-flight spectroscopy. This technique is combined with two-photon photoluminescence fluctuation correlation spectroscopy (TPPL-FCS) to simultaneously monitor the optical and hydrodynamic behaviour of these nano-assemblies in solution, with single-particle sensitivity and microsecond temporal resolution. In this study, the AuNPs have an average core diameter of 12 nm, which renders their dark-field plasmonic light scattering too weak for single-particle imaging. Moreover, as a result of the lack of plasmonic coupling in the dimers, the optical extinction, scattering and photoluminescence spectra of the DNA-AuNP complexes are not sufficiently different to distinguish between monomers and dimers. The use of TPPL-FCS successfully addresses these bottlenecks and enables the distinction between AuNP monomers and AuNP dimers in solution by measurement of their hydrodynamic rotational and translational diffusion.
通过光子飞行时间光谱法获得了DNA-金纳米颗粒(AuNP)单共轭物以及相应的DNA连接的AuNP二聚体的双光子光致发光(TPPL)发射光谱。该技术与双光子光致发光涨落相关光谱法(TPPL-FCS)相结合,以单粒子灵敏度和微秒级时间分辨率同时监测这些纳米组装体在溶液中的光学和流体动力学行为。在本研究中,AuNP的平均核心直径为12 nm,这使得它们的暗场等离子体光散射对于单粒子成像来说太弱。此外,由于二聚体中缺乏等离子体耦合,DNA-AuNP复合物的光学消光、散射和光致发光光谱差异不足,无法区分单体和二聚体。TPPL-FCS的使用成功解决了这些瓶颈问题,并通过测量AuNP单体和AuNP二聚体在溶液中的流体动力学旋转和平动扩散来区分它们。