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Spectral image scanning microscopy

For decades, the confocal microscope has represented one of the dominant imaging systems in biomedical imaging at sub-cellular lengthscales. Recently, however, it has increasingly been replaced by a related, but more powerful successor technique termed image scanning microscopy (ISM). In this articl...

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Detalles Bibliográficos
Autores principales: Strasser, Franziska, Offterdinger, Martin, Piestun, Rafael, Jesacher, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Optical Society of America 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6524570/
https://www.ncbi.nlm.nih.gov/pubmed/31143501
http://dx.doi.org/10.1364/BOE.10.002513
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author Strasser, Franziska
Offterdinger, Martin
Piestun, Rafael
Jesacher, Alexander
author_facet Strasser, Franziska
Offterdinger, Martin
Piestun, Rafael
Jesacher, Alexander
author_sort Strasser, Franziska
collection PubMed
description For decades, the confocal microscope has represented one of the dominant imaging systems in biomedical imaging at sub-cellular lengthscales. Recently, however, it has increasingly been replaced by a related, but more powerful successor technique termed image scanning microscopy (ISM). In this article, we present ISM capable of measuring spectroscopic information such as that contained in fluorescence or Raman images. Compared to established confocal spectroscopic imaging systems, our implementation offers similar spectral resolution, but higher spatial resolution and detection efficiency. Color sensitivity is achieved by a grating placed in the detection path in conjunction with a camera collecting both spatial and spectral information. The multidimensional data is processed using multi-view maximum likelihood image reconstruction. Our findings are supported by numerical simulations and experiments on micro beads and double-stained HeLa cells.
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spelling pubmed-65245702019-05-29 Spectral image scanning microscopy Strasser, Franziska Offterdinger, Martin Piestun, Rafael Jesacher, Alexander Biomed Opt Express Article For decades, the confocal microscope has represented one of the dominant imaging systems in biomedical imaging at sub-cellular lengthscales. Recently, however, it has increasingly been replaced by a related, but more powerful successor technique termed image scanning microscopy (ISM). In this article, we present ISM capable of measuring spectroscopic information such as that contained in fluorescence or Raman images. Compared to established confocal spectroscopic imaging systems, our implementation offers similar spectral resolution, but higher spatial resolution and detection efficiency. Color sensitivity is achieved by a grating placed in the detection path in conjunction with a camera collecting both spatial and spectral information. The multidimensional data is processed using multi-view maximum likelihood image reconstruction. Our findings are supported by numerical simulations and experiments on micro beads and double-stained HeLa cells. Optical Society of America 2019-04-22 /pmc/articles/PMC6524570/ /pubmed/31143501 http://dx.doi.org/10.1364/BOE.10.002513 Text en Published by The Optical Society under the terms of the Creative Commons Attribution 4.0 License. Further distribution of this work must maintain attribution to the author(s) and the published article's title, journal citation, and DOI. Published by The Optical Society under the terms of the Creative Commons Attribution 4.0 License (http://creativecommons.org/licenses/by/4.0/) . Further distribution of this work must maintain attribution to the author(s) and the published article's title, journal citation, and DOI.
spellingShingle Article
Strasser, Franziska
Offterdinger, Martin
Piestun, Rafael
Jesacher, Alexander
Spectral image scanning microscopy
title Spectral image scanning microscopy
title_full Spectral image scanning microscopy
title_fullStr Spectral image scanning microscopy
title_full_unstemmed Spectral image scanning microscopy
title_short Spectral image scanning microscopy
title_sort spectral image scanning microscopy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6524570/
https://www.ncbi.nlm.nih.gov/pubmed/31143501
http://dx.doi.org/10.1364/BOE.10.002513
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