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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Academic Press
2015
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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. |
format | Online Article Text |
id | pubmed-4641873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Academic Press |
record_format | MEDLINE/PubMed |
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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