论文标题
金纳米棒上的异常DNA杂交动力学通过双重单分子成像和opopoprasmonic传感平台揭示
Anomalous DNA hybridisation kinetics on gold nanorods revealed via a dual single-molecule imaging and optoplasmonic sensing platform
论文作者
论文摘要
观察固定在等离子纳米颗粒上的DNA探针的杂交动力学是PLAMON增强的荧光检测,从弱发射物种中检测到荧光检测,而基于折射率的单分子检测到Optoplasmonic传感器。详细研究了局部场在提供单分子检测的等离子信号增强方面的作用。然而,很少有研究比较两种技术的实验结果用于单分子研究。在这里,我们开发了第一个光学设置,该光学设置集成了基于寡核苷酸的基于Optoprasmonic和基于DNA斑点的检测,以比较这些子平台,并将互补的见解与单分子过程相互补。我们记录了单个瞬态杂交事件的荧光和光质传感器信号。在同一样品细胞和长时间(即朝着高结合位点占用率)中观察到杂交事件。据报道,在测量持续时间内,关联率降低。我们的双光质传感和成像平台提供了对观察到的现象的洞察力,揭示了不可逆的杂交事件在Optoprasmonic传感中积累的不可逆杂交事件。我们的结果表明,新型的物理化学机制导致在光学激发的等离子纳米颗粒上稳定DNA杂交。
Observing the hybridisation kinetics of DNA probes immobilised on plasmonic nanoparticles is key in plamon enhanced fluorescence detection from weak emitting species, and refractive index based single-molecule detection on optoplasmonic sensors. The role of the local field in providing plasmonic signal enhancements for single-molecule detection has been studied in great detail. Nevertheless, few studies have compared the experimental results in both techniques for single-molecule studies. Here we developed the first optical setup that integrates optoplasmonic and DNA-PAINT based detection of oligonucleotides to compare these sub-platforms and provide complementary insights into single-molecule processes. We record the fluorescence and optoplasmonic sensor signals for individual, transient hybridisation events. The hybridisation events are observed in the same sample cell and over a prolonged time (i.e. towards high binding site occupancies). A decrease in the association rate over the measurement duration is reported. Our dual optoplasmonic sensing and imaging platform offers insight into the observed phenomenon, revealing that irreversible hybridisation events accumulate over detected step signals in optoplasmonic sensing. Our results point to novel physicochemical mechanisms that result in the stabilisation of DNA hybridisation on optically-excited plasmonic nanoparticles.