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Miniature scanning light-sheet illumination implemented in a conventional microscope
Living cells are highly dynamic systems responding to a large variety of biochemical and mechanical stimuli over minutes, which are well controlled by e.g. optical tweezers. However, live cell investigation through fluorescence microscopy is usually limited not only by the spatial and temporal imagi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Optical Society of America
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6157761/ https://www.ncbi.nlm.nih.gov/pubmed/30615716 http://dx.doi.org/10.1364/BOE.9.004263 |
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author | Kashekodi, Anjan Bhat Meinert, Tobias Michiels, Rebecca Rohrbach, Alexander |
author_facet | Kashekodi, Anjan Bhat Meinert, Tobias Michiels, Rebecca Rohrbach, Alexander |
author_sort | Kashekodi, Anjan Bhat |
collection | PubMed |
description | Living cells are highly dynamic systems responding to a large variety of biochemical and mechanical stimuli over minutes, which are well controlled by e.g. optical tweezers. However, live cell investigation through fluorescence microscopy is usually limited not only by the spatial and temporal imaging resolution but also by fluorophore bleaching. Therefore, we designed a miniature light-sheet illumination system that is implemented in a conventional inverted microscope equipped with optical tweezers and interferometric tracking to capture 3D images of living macrophages at reduced bleaching. The horizontal light-sheet is generated with a 0.12 mm small cantilevered mirror placed at 45° to the detection axis. The objective launched illumination beam is reflected by the micro-mirror and illuminates the sample perpendicular to the detection axis. Lateral and axial scanning of both Gaussian and Bessel beams, together with an electrically tunable lens for fast focusing, enables rapid 3D image capture without moving the sample or the objective lens. Using scanned Bessel beams and line-confocal detection, an average axial resolution of 0.8 µm together with a 10-15 fold improved image contrast is achieved. |
format | Online Article Text |
id | pubmed-6157761 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Optical Society of America |
record_format | MEDLINE/PubMed |
spelling | pubmed-61577612018-09-27 Miniature scanning light-sheet illumination implemented in a conventional microscope Kashekodi, Anjan Bhat Meinert, Tobias Michiels, Rebecca Rohrbach, Alexander Biomed Opt Express Article Living cells are highly dynamic systems responding to a large variety of biochemical and mechanical stimuli over minutes, which are well controlled by e.g. optical tweezers. However, live cell investigation through fluorescence microscopy is usually limited not only by the spatial and temporal imaging resolution but also by fluorophore bleaching. Therefore, we designed a miniature light-sheet illumination system that is implemented in a conventional inverted microscope equipped with optical tweezers and interferometric tracking to capture 3D images of living macrophages at reduced bleaching. The horizontal light-sheet is generated with a 0.12 mm small cantilevered mirror placed at 45° to the detection axis. The objective launched illumination beam is reflected by the micro-mirror and illuminates the sample perpendicular to the detection axis. Lateral and axial scanning of both Gaussian and Bessel beams, together with an electrically tunable lens for fast focusing, enables rapid 3D image capture without moving the sample or the objective lens. Using scanned Bessel beams and line-confocal detection, an average axial resolution of 0.8 µm together with a 10-15 fold improved image contrast is achieved. Optical Society of America 2018-08-14 /pmc/articles/PMC6157761/ /pubmed/30615716 http://dx.doi.org/10.1364/BOE.9.004263 Text en © 2018 Optical Society of America under the terms of the OSA Open Access Publishing Agreement © 2018 Optical Society of America under the terms of the OSA Open Access Publishing Agreement (https://doi.org/10.1364/OA_License_v1) |
spellingShingle | Article Kashekodi, Anjan Bhat Meinert, Tobias Michiels, Rebecca Rohrbach, Alexander Miniature scanning light-sheet illumination implemented in a conventional microscope |
title | Miniature scanning light-sheet illumination implemented in a conventional microscope |
title_full | Miniature scanning light-sheet illumination implemented in a conventional microscope |
title_fullStr | Miniature scanning light-sheet illumination implemented in a conventional microscope |
title_full_unstemmed | Miniature scanning light-sheet illumination implemented in a conventional microscope |
title_short | Miniature scanning light-sheet illumination implemented in a conventional microscope |
title_sort | miniature scanning light-sheet illumination implemented in a conventional microscope |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6157761/ https://www.ncbi.nlm.nih.gov/pubmed/30615716 http://dx.doi.org/10.1364/BOE.9.004263 |
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