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Scanning thin-sheet laser imaging microscopy (sTSLIM) with structured illumination and HiLo background rejection.
We report replacement of one side of a static illumination, dual sided, thin-sheet laser imaging microscope (TSLIM) with an intensity modulated laser scanner in order to implement structured illumination (SI) and HiLo image demodulation techniques for background rejection. The new system is equipped...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Optical Society of America
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3255335/ https://www.ncbi.nlm.nih.gov/pubmed/22254177 http://dx.doi.org/10.1364/BOE.3.000170 |
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author | Schröter, Tobias J. Johnson, Shane B. John, Kerstin Santi, Peter A. |
author_facet | Schröter, Tobias J. Johnson, Shane B. John, Kerstin Santi, Peter A. |
author_sort | Schröter, Tobias J. |
collection | PubMed |
description | We report replacement of one side of a static illumination, dual sided, thin-sheet laser imaging microscope (TSLIM) with an intensity modulated laser scanner in order to implement structured illumination (SI) and HiLo image demodulation techniques for background rejection. The new system is equipped with one static and one scanned light-sheet and is called a scanning thin-sheet laser imaging microscope (sTSLIM). It is an optimized version of a light-sheet fluorescent microscope that is designed to image large specimens (<15 mm in diameter). In this paper we describe the hardware and software modifications to TSLIM that allow for static and uniform light-sheet illumination with SI and HiLo image demodulation. The static light-sheet has a thickness of 3.2 µm; whereas, the scanned side has a light-sheet thickness of 4.2 µm. The scanned side images specimens with subcellular resolution (<1 µm lateral and <4 µm axial resolution) with a size up to 15 mm. SI and HiLo produce superior contrast compared to both the uniform static and scanned light-sheets. HiLo contrast was greater than SI and is faster and more robust than SI because as it produces images in two-thirds of the time and exhibits fewer intensity streaking artifacts. |
format | Online Article Text |
id | pubmed-3255335 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Optical Society of America |
record_format | MEDLINE/PubMed |
spelling | pubmed-32553352012-01-17 Scanning thin-sheet laser imaging microscopy (sTSLIM) with structured illumination and HiLo background rejection. Schröter, Tobias J. Johnson, Shane B. John, Kerstin Santi, Peter A. Biomed Opt Express Microscopy We report replacement of one side of a static illumination, dual sided, thin-sheet laser imaging microscope (TSLIM) with an intensity modulated laser scanner in order to implement structured illumination (SI) and HiLo image demodulation techniques for background rejection. The new system is equipped with one static and one scanned light-sheet and is called a scanning thin-sheet laser imaging microscope (sTSLIM). It is an optimized version of a light-sheet fluorescent microscope that is designed to image large specimens (<15 mm in diameter). In this paper we describe the hardware and software modifications to TSLIM that allow for static and uniform light-sheet illumination with SI and HiLo image demodulation. The static light-sheet has a thickness of 3.2 µm; whereas, the scanned side has a light-sheet thickness of 4.2 µm. The scanned side images specimens with subcellular resolution (<1 µm lateral and <4 µm axial resolution) with a size up to 15 mm. SI and HiLo produce superior contrast compared to both the uniform static and scanned light-sheets. HiLo contrast was greater than SI and is faster and more robust than SI because as it produces images in two-thirds of the time and exhibits fewer intensity streaking artifacts. Optical Society of America 2011-12-19 /pmc/articles/PMC3255335/ /pubmed/22254177 http://dx.doi.org/10.1364/BOE.3.000170 Text en ©2011 Optical Society of America http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 Unported License, which permits download and redistribution, provided that the original work is properly cited. This license restricts the article from being modified or used commercially. |
spellingShingle | Microscopy Schröter, Tobias J. Johnson, Shane B. John, Kerstin Santi, Peter A. Scanning thin-sheet laser imaging microscopy (sTSLIM) with structured illumination and HiLo background rejection. |
title | Scanning thin-sheet laser imaging microscopy (sTSLIM) with structured illumination and HiLo background rejection. |
title_full | Scanning thin-sheet laser imaging microscopy (sTSLIM) with structured illumination and HiLo background rejection. |
title_fullStr | Scanning thin-sheet laser imaging microscopy (sTSLIM) with structured illumination and HiLo background rejection. |
title_full_unstemmed | Scanning thin-sheet laser imaging microscopy (sTSLIM) with structured illumination and HiLo background rejection. |
title_short | Scanning thin-sheet laser imaging microscopy (sTSLIM) with structured illumination and HiLo background rejection. |
title_sort | scanning thin-sheet laser imaging microscopy (stslim) with structured illumination and hilo background rejection. |
topic | Microscopy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3255335/ https://www.ncbi.nlm.nih.gov/pubmed/22254177 http://dx.doi.org/10.1364/BOE.3.000170 |
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