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Construction of an instant structured illumination microscope

A challenge in biological imaging is to capture high-resolution images at fast frame rates in live cells. The “instant structured illumination microscope” (iSIM) is a system designed for this purpose. Similarly to standard structured illumination microscopy (SIM), an iSIM provides a twofold improvem...

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Autores principales: Curd, Alistair, Cleasby, Alexa, Makowska, Katarzyna, York, Andrew, Shroff, Hari, Peckham, Michelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4641873/
https://www.ncbi.nlm.nih.gov/pubmed/26210400
http://dx.doi.org/10.1016/j.ymeth.2015.07.012
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author Curd, Alistair
Cleasby, Alexa
Makowska, Katarzyna
York, Andrew
Shroff, Hari
Peckham, Michelle
author_facet Curd, Alistair
Cleasby, Alexa
Makowska, Katarzyna
York, Andrew
Shroff, Hari
Peckham, Michelle
author_sort Curd, Alistair
collection PubMed
description A challenge in biological imaging is to capture high-resolution images at fast frame rates in live cells. The “instant structured illumination microscope” (iSIM) is a system designed for this purpose. Similarly to standard structured illumination microscopy (SIM), an iSIM provides a twofold improvement over widefield microscopy, in x, y and z, but also allows much faster image acquisition, with real-time display of super-resolution images. The assembly of an iSIM is reasonably complex, involving the combination and alignment of many optical components, including three micro-optics arrays (two lenslet arrays and an array of pinholes, all with a pitch of 222 μm) and a double-sided scanning mirror. In addition, a number of electronic components must be correctly controlled. Construction of the system is therefore not trivial, but is highly desirable, particularly for live-cell imaging. We report, and provide instructions for, the construction of an iSIM, including minor modifications to a previous design in both hardware and software. The final instrument allows us to rapidly acquire fluorescence images at rates faster than 100 fps, with approximately twofold improvement in resolution in both x–y and z; sub-diffractive biological features have an apparent size (full width at half maximum) of 145 nm (lateral) and 320 nm (axial), using a 1.49 NA objective and 488 nm excitation.
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spelling pubmed-46418732015-12-03 Construction of an instant structured illumination microscope Curd, Alistair Cleasby, Alexa Makowska, Katarzyna York, Andrew Shroff, Hari Peckham, Michelle Methods Article A challenge in biological imaging is to capture high-resolution images at fast frame rates in live cells. The “instant structured illumination microscope” (iSIM) is a system designed for this purpose. Similarly to standard structured illumination microscopy (SIM), an iSIM provides a twofold improvement over widefield microscopy, in x, y and z, but also allows much faster image acquisition, with real-time display of super-resolution images. The assembly of an iSIM is reasonably complex, involving the combination and alignment of many optical components, including three micro-optics arrays (two lenslet arrays and an array of pinholes, all with a pitch of 222 μm) and a double-sided scanning mirror. In addition, a number of electronic components must be correctly controlled. Construction of the system is therefore not trivial, but is highly desirable, particularly for live-cell imaging. We report, and provide instructions for, the construction of an iSIM, including minor modifications to a previous design in both hardware and software. The final instrument allows us to rapidly acquire fluorescence images at rates faster than 100 fps, with approximately twofold improvement in resolution in both x–y and z; sub-diffractive biological features have an apparent size (full width at half maximum) of 145 nm (lateral) and 320 nm (axial), using a 1.49 NA objective and 488 nm excitation. Academic Press 2015-10-15 /pmc/articles/PMC4641873/ /pubmed/26210400 http://dx.doi.org/10.1016/j.ymeth.2015.07.012 Text en © 2015 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Curd, Alistair
Cleasby, Alexa
Makowska, Katarzyna
York, Andrew
Shroff, Hari
Peckham, Michelle
Construction of an instant structured illumination microscope
title Construction of an instant structured illumination microscope
title_full Construction of an instant structured illumination microscope
title_fullStr Construction of an instant structured illumination microscope
title_full_unstemmed Construction of an instant structured illumination microscope
title_short Construction of an instant structured illumination microscope
title_sort construction of an instant structured illumination microscope
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4641873/
https://www.ncbi.nlm.nih.gov/pubmed/26210400
http://dx.doi.org/10.1016/j.ymeth.2015.07.012
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