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A Guide to Structured Illumination TIRF Microscopy at High Speed with Multiple Colors
Optical super-resolution imaging with structured illumination microscopy (SIM) is a key technology for the visualization of processes at the molecular level in the chemical and biomedical sciences. Although commercial SIM systems are available, systems that are custom designed in the laboratory can...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MyJove Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4927749/ https://www.ncbi.nlm.nih.gov/pubmed/27285848 http://dx.doi.org/10.3791/53988 |
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author | Young, Laurence J. Ströhl, Florian Kaminski, Clemens F. |
author_facet | Young, Laurence J. Ströhl, Florian Kaminski, Clemens F. |
author_sort | Young, Laurence J. |
collection | PubMed |
description | Optical super-resolution imaging with structured illumination microscopy (SIM) is a key technology for the visualization of processes at the molecular level in the chemical and biomedical sciences. Although commercial SIM systems are available, systems that are custom designed in the laboratory can outperform commercial systems, the latter typically designed for ease of use and general purpose applications, both in terms of imaging fidelity and speed. This article presents an in-depth guide to building a SIM system that uses total internal reflection (TIR) illumination and is capable of imaging at up to 10 Hz in three colors at a resolution reaching 100 nm. Due to the combination of SIM and TIRF, the system provides better image contrast than rival technologies. To achieve these specifications, several optical elements are used to enable automated control over the polarization state and spatial structure of the illumination light for all available excitation wavelengths. Full details on hardware implementation and control are given to achieve synchronization between excitation light pattern generation, wavelength, polarization state, and camera control with an emphasis on achieving maximum acquisition frame rate. A step-by-step protocol for system alignment and calibration is presented and the achievable resolution improvement is validated on ideal test samples. The capability for video-rate super-resolution imaging is demonstrated with living cells. |
format | Online Article Text |
id | pubmed-4927749 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MyJove Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-49277492016-07-12 A Guide to Structured Illumination TIRF Microscopy at High Speed with Multiple Colors Young, Laurence J. Ströhl, Florian Kaminski, Clemens F. J Vis Exp Bioengineering Optical super-resolution imaging with structured illumination microscopy (SIM) is a key technology for the visualization of processes at the molecular level in the chemical and biomedical sciences. Although commercial SIM systems are available, systems that are custom designed in the laboratory can outperform commercial systems, the latter typically designed for ease of use and general purpose applications, both in terms of imaging fidelity and speed. This article presents an in-depth guide to building a SIM system that uses total internal reflection (TIR) illumination and is capable of imaging at up to 10 Hz in three colors at a resolution reaching 100 nm. Due to the combination of SIM and TIRF, the system provides better image contrast than rival technologies. To achieve these specifications, several optical elements are used to enable automated control over the polarization state and spatial structure of the illumination light for all available excitation wavelengths. Full details on hardware implementation and control are given to achieve synchronization between excitation light pattern generation, wavelength, polarization state, and camera control with an emphasis on achieving maximum acquisition frame rate. A step-by-step protocol for system alignment and calibration is presented and the achievable resolution improvement is validated on ideal test samples. The capability for video-rate super-resolution imaging is demonstrated with living cells. MyJove Corporation 2016-05-30 /pmc/articles/PMC4927749/ /pubmed/27285848 http://dx.doi.org/10.3791/53988 Text en Copyright © 2016, Journal of Visualized Experiments http://creativecommons.org/licenses/by/3.0/us/ This is an open-access article distributed under the terms of the Creative Commons Attribution 3.0 License. To view a copy of this license, visithttp://creativecommons.org/licenses/by/3.0/us/ |
spellingShingle | Bioengineering Young, Laurence J. Ströhl, Florian Kaminski, Clemens F. A Guide to Structured Illumination TIRF Microscopy at High Speed with Multiple Colors |
title | A Guide to Structured Illumination TIRF Microscopy at High Speed with Multiple Colors |
title_full | A Guide to Structured Illumination TIRF Microscopy at High Speed with Multiple Colors |
title_fullStr | A Guide to Structured Illumination TIRF Microscopy at High Speed with Multiple Colors |
title_full_unstemmed | A Guide to Structured Illumination TIRF Microscopy at High Speed with Multiple Colors |
title_short | A Guide to Structured Illumination TIRF Microscopy at High Speed with Multiple Colors |
title_sort | guide to structured illumination tirf microscopy at high speed with multiple colors |
topic | Bioengineering |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4927749/ https://www.ncbi.nlm.nih.gov/pubmed/27285848 http://dx.doi.org/10.3791/53988 |
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