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Label-Free Aptasensor Based on Ultrathin-Linker-Mediated Hot-Spot Assembly To Induce Strong Directional Fluorescence
65
Citations
45
References
2014
Year
NanoparticlesEngineeringMetal NanoparticlesUltrathin-linker-mediated Hot-spot AssemblySurface-enhanced Raman ScatteringMolecular BiologyNanomedicineBiosensing SystemsNanosensorChemical SensorBiophysicsPlasmonic MaterialLabel-free BiosensorNanotechnologyStrong Directional FluorescenceSingle-molecule DetectionBiomolecular EngineeringPlasmonicsBiomedical DiagnosticsNanomaterialsSilver NanoparticlesLabel-free AptasensorChemical ProbePlasmonic Assembly
We have demonstrated the proof-of-concept of a label-free biosensor based on emission induced by an extreme hot-spot plasmonic assembly. In this work, an ultrathin linking layer composed of cationic polymers and aptamers was fabricated to mediate the assembly of a silver nanoparticles (AgNPs)-dyes-gold film with a strongly coupled architecture through sensing a target protein. Generation of directional surface plasmon coupled emission (SPCE) was thus stimulated as a means of reporting biorecognition. Both the biomolecules and the nanoparticles were totally free of labeling, thereby ensuring the activity of biomolecules and allowing the use of freshly prepared metallic nanoparticles with large dimensions. This sensor smartly prevents the plasmonic assembly in the absence of targets, thus maintaining no signal through quenching fluorophores loaded onto a gold film. In the presence of targets, the ultrathin layer is activated to link NPs-film junctions. The small gap of the junction (no greater than 2 nm) and the large diameter of the nanoparticles (~100 nm) ensure that ultrastrong coupling is achieved to generate intense SPCE. A >500-fold enhancement of the signal was observed in the biosensing. This strategy provides a simple, reliable, and effective way to apply plasmonic nanostructures in the development of biosensing.
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