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High-resolution imaging of a cell-attached nanointerface using a gold-nanoparticle two-dimensional sheet

This paper proposes a simple, effective, non-scanning method for the visualization of a cell-attached nanointerface. The method uses localized surface plasmon resonance (LSPR) excited homogeneously on a two-dimensional (2D) self-assembled gold-nanoparticle sheet. The LSPR of the gold-nanoparticle sh...

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Detalles Bibliográficos
Autores principales: Masuda, Shihomi, Yanase, Yuhki, Usukura, Eiji, Ryuzaki, Sou, Wang, Pangpang, Okamoto, Koichi, Kuboki, Thasaneeya, Kidoaki, Satoru, Tamada, Kaoru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5473937/
https://www.ncbi.nlm.nih.gov/pubmed/28623338
http://dx.doi.org/10.1038/s41598-017-04000-4
Descripción
Sumario:This paper proposes a simple, effective, non-scanning method for the visualization of a cell-attached nanointerface. The method uses localized surface plasmon resonance (LSPR) excited homogeneously on a two-dimensional (2D) self-assembled gold-nanoparticle sheet. The LSPR of the gold-nanoparticle sheet provides high-contrast interfacial images due to the confined light within a region a few tens of nanometers from the particles and the enhancement of fluorescence. Test experiments on rat basophilic leukemia (RBL-2H3) cells with fluorescence-labeled actin filaments revealed high axial and lateral resolution even under a regular epifluorescence microscope, which produced higher quality images than those captured under a total internal reflection fluorescence (TIRF) microscope. This non-scanning-type, high-resolution imaging method will be an effective tool for monitoring interfacial phenomena that exhibit relatively rapid reaction kinetics in various cellular and molecular dynamics.