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Super-resolution imaging using nano-bells

In this paper we demonstrate a new scheme for optical super-resolution, inspired, in-part, by PALM and STORM. In this scheme each object in the field of view is tagged with a signal that allows them to be detected separately. By doing this we can identify and locate each object separately with signi...

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Autores principales: Fuentes-Domínguez, Rafael, Pérez-Cota, Fernando, Naznin, Shakila, Smith, Richard J., Clark, Matt
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219565/
https://www.ncbi.nlm.nih.gov/pubmed/30401881
http://dx.doi.org/10.1038/s41598-018-34744-6
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author Fuentes-Domínguez, Rafael
Pérez-Cota, Fernando
Naznin, Shakila
Smith, Richard J.
Clark, Matt
author_facet Fuentes-Domínguez, Rafael
Pérez-Cota, Fernando
Naznin, Shakila
Smith, Richard J.
Clark, Matt
author_sort Fuentes-Domínguez, Rafael
collection PubMed
description In this paper we demonstrate a new scheme for optical super-resolution, inspired, in-part, by PALM and STORM. In this scheme each object in the field of view is tagged with a signal that allows them to be detected separately. By doing this we can identify and locate each object separately with significantly higher resolution than the diffraction limit. We demonstrate this by imaging nanoparticles significantly smaller than the optical resolution limit. In this case the “tag” we have used is the frequency of vibration of nanoscale “bells” made of metallic nanoparticles whose acoustic vibrational frequency is in the multi-GHz range. Since the vibration of the particles can be easily excited and detected and the frequency is directly related to the particle size, we can separate the signals from many particles of sufficiently different sizes even though they are smaller than, and separated by less than, the optical resolution limit. Using this scheme we have been able to localise the nanoparticle position with a precision of ~3 nm. This has many potential advantages - such nanoparticles are easily inserted into cells and well tolerated, the particles do not bleach and can be produced easily with very dispersed sizes. We estimate that 50 or more different particles (or frequency channels) can be accessed in each optical point spread function using the vibrational frequencies of gold nanospheres. However, many more channels may be accessed using more complex structures (such as nanorods) and detection techniques (for instance using polarization or wavelength selective detection) opening up this technique as a generalized method of achieving super-optical resolution imaging.
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spelling pubmed-62195652018-11-07 Super-resolution imaging using nano-bells Fuentes-Domínguez, Rafael Pérez-Cota, Fernando Naznin, Shakila Smith, Richard J. Clark, Matt Sci Rep Article In this paper we demonstrate a new scheme for optical super-resolution, inspired, in-part, by PALM and STORM. In this scheme each object in the field of view is tagged with a signal that allows them to be detected separately. By doing this we can identify and locate each object separately with significantly higher resolution than the diffraction limit. We demonstrate this by imaging nanoparticles significantly smaller than the optical resolution limit. In this case the “tag” we have used is the frequency of vibration of nanoscale “bells” made of metallic nanoparticles whose acoustic vibrational frequency is in the multi-GHz range. Since the vibration of the particles can be easily excited and detected and the frequency is directly related to the particle size, we can separate the signals from many particles of sufficiently different sizes even though they are smaller than, and separated by less than, the optical resolution limit. Using this scheme we have been able to localise the nanoparticle position with a precision of ~3 nm. This has many potential advantages - such nanoparticles are easily inserted into cells and well tolerated, the particles do not bleach and can be produced easily with very dispersed sizes. We estimate that 50 or more different particles (or frequency channels) can be accessed in each optical point spread function using the vibrational frequencies of gold nanospheres. However, many more channels may be accessed using more complex structures (such as nanorods) and detection techniques (for instance using polarization or wavelength selective detection) opening up this technique as a generalized method of achieving super-optical resolution imaging. Nature Publishing Group UK 2018-11-06 /pmc/articles/PMC6219565/ /pubmed/30401881 http://dx.doi.org/10.1038/s41598-018-34744-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Fuentes-Domínguez, Rafael
Pérez-Cota, Fernando
Naznin, Shakila
Smith, Richard J.
Clark, Matt
Super-resolution imaging using nano-bells
title Super-resolution imaging using nano-bells
title_full Super-resolution imaging using nano-bells
title_fullStr Super-resolution imaging using nano-bells
title_full_unstemmed Super-resolution imaging using nano-bells
title_short Super-resolution imaging using nano-bells
title_sort super-resolution imaging using nano-bells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219565/
https://www.ncbi.nlm.nih.gov/pubmed/30401881
http://dx.doi.org/10.1038/s41598-018-34744-6
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