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Enhancing multi-spot structured illumination microscopy with fluorescence difference

Structured illumination microscopy is a super-resolution technique used extensively in biological research. However, this technique is limited in the maximum possible resolution increase. Here we report the results of simulations of a novel enhanced multi-spot structured illumination technique. This...

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Detalles Bibliográficos
Autores principales: Ward, Edward N., Torkelsen, Frida H., Pal, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society Publishing 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5882675/
https://www.ncbi.nlm.nih.gov/pubmed/29657751
http://dx.doi.org/10.1098/rsos.171336
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author Ward, Edward N.
Torkelsen, Frida H.
Pal, Robert
author_facet Ward, Edward N.
Torkelsen, Frida H.
Pal, Robert
author_sort Ward, Edward N.
collection PubMed
description Structured illumination microscopy is a super-resolution technique used extensively in biological research. However, this technique is limited in the maximum possible resolution increase. Here we report the results of simulations of a novel enhanced multi-spot structured illumination technique. This method combines the super-resolution technique of difference microscopy with structured illumination deconvolution. Initial results give at minimum a 1.4-fold increase in resolution over conventional structured illumination in a low-noise environment. This new technique also has the potential to be expanded to further enhance axial resolution with three-dimensional difference microscopy. The requirement for precise pattern determination in this technique also led to the development of a new pattern estimation algorithm which proved more efficient and reliable than other methods tested.
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spelling pubmed-58826752018-04-13 Enhancing multi-spot structured illumination microscopy with fluorescence difference Ward, Edward N. Torkelsen, Frida H. Pal, Robert R Soc Open Sci Chemistry Structured illumination microscopy is a super-resolution technique used extensively in biological research. However, this technique is limited in the maximum possible resolution increase. Here we report the results of simulations of a novel enhanced multi-spot structured illumination technique. This method combines the super-resolution technique of difference microscopy with structured illumination deconvolution. Initial results give at minimum a 1.4-fold increase in resolution over conventional structured illumination in a low-noise environment. This new technique also has the potential to be expanded to further enhance axial resolution with three-dimensional difference microscopy. The requirement for precise pattern determination in this technique also led to the development of a new pattern estimation algorithm which proved more efficient and reliable than other methods tested. The Royal Society Publishing 2018-03-14 /pmc/articles/PMC5882675/ /pubmed/29657751 http://dx.doi.org/10.1098/rsos.171336 Text en © 2018 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Chemistry
Ward, Edward N.
Torkelsen, Frida H.
Pal, Robert
Enhancing multi-spot structured illumination microscopy with fluorescence difference
title Enhancing multi-spot structured illumination microscopy with fluorescence difference
title_full Enhancing multi-spot structured illumination microscopy with fluorescence difference
title_fullStr Enhancing multi-spot structured illumination microscopy with fluorescence difference
title_full_unstemmed Enhancing multi-spot structured illumination microscopy with fluorescence difference
title_short Enhancing multi-spot structured illumination microscopy with fluorescence difference
title_sort enhancing multi-spot structured illumination microscopy with fluorescence difference
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5882675/
https://www.ncbi.nlm.nih.gov/pubmed/29657751
http://dx.doi.org/10.1098/rsos.171336
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