Multiplane Encoded Light-Sheet Microscopy for Enhanced 3D Imaging
Light-sheet microscopes have become the tool of choice for volumetric imaging of large samples. Based on a wide-field acquisition scheme, they are capable of optical sectioning at diffraction-limited resolution and minimal overall photodamage. Unfortunately, traditional architectures are limited in...
| Autores: | , , , , , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2021 |
| País: | España |
| Institución: | Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
| Repositorio: | Recercat. Dipósit de la Recerca de Catalunya |
| OAI Identifier: | oai:recercat.cat:2445/183314 |
| Acceso en línea: | https://hdl.handle.net/2445/183314 |
| Access Level: | acceso abierto |
| Palabra clave: | Microscopis Visualització tridimensional Microscopes Three-dimensional display systems |
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Multiplane Encoded Light-Sheet Microscopy for Enhanced 3D ImagingZunino, AlessandroGarzella, FrancescoTrianni, AlbertaSaggau, PeterBianchini, PaoloDiaspro, AlbertoDuocastella, MartíMicroscopisVisualització tridimensionalMicroscopesThree-dimensional display systemsLight-sheet microscopes have become the tool of choice for volumetric imaging of large samples. Based on a wide-field acquisition scheme, they are capable of optical sectioning at diffraction-limited resolution and minimal overall photodamage. Unfortunately, traditional architectures are limited in speed because 3D images are collected by either sample translation or synchronized movement of both light-sheet and detection objective lens. A promising solution avoiding slow mechanical movements is to extend the depth-of-field of the microscope and moving only the light-sheet. However, this normally comes at the cost of losing light and contrast, compromising the signal-to-noise ratio of the images. Here, we propose an innovative technique devoted to restoring the quality of the images, while preserving the speed of extended depth-of-field microscopes. It is based on generating a stack of parallel light-sheets using a pair of orthogonal acousto-optic deflectors, enabling the simultaneous illumination of different sample planes. Given the extended depth-of-field, all such planes appear in focus and can be acquired in a superimposed single frame. By applying a single-step inversion algorithm, we can decode a stack of frames into a volumetric image whose signal-to-noise ratio and contrast are greatly enhanced. We provide a detailed theoretical framework of the method and demonstrate its feasibility with volumetric images of kidney cell spheroids.American Chemical Society2022202220212022info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://hdl.handle.net/2445/183314Articles publicats en revistes (Física Aplicada)reponame:Recercat. Dipósit de la Recerca de Catalunyainstname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)InglésReproducció del document publicat a: https://doi.org/10.1021/acsphotonics.1c01401ACS Photonics, 2021https://doi.org/10.1021/acsphotonics.1c01401(c) Zunino, Alessandro, et al., 2021info:eu-repo/semantics/openAccessoai:recercat.cat:2445/1833142026-05-29T05:05:01Z |
| dc.title.none.fl_str_mv |
Multiplane Encoded Light-Sheet Microscopy for Enhanced 3D Imaging |
| title |
Multiplane Encoded Light-Sheet Microscopy for Enhanced 3D Imaging |
| spellingShingle |
Multiplane Encoded Light-Sheet Microscopy for Enhanced 3D Imaging Zunino, Alessandro Microscopis Visualització tridimensional Microscopes Three-dimensional display systems |
| title_short |
Multiplane Encoded Light-Sheet Microscopy for Enhanced 3D Imaging |
| title_full |
Multiplane Encoded Light-Sheet Microscopy for Enhanced 3D Imaging |
| title_fullStr |
Multiplane Encoded Light-Sheet Microscopy for Enhanced 3D Imaging |
| title_full_unstemmed |
Multiplane Encoded Light-Sheet Microscopy for Enhanced 3D Imaging |
| title_sort |
Multiplane Encoded Light-Sheet Microscopy for Enhanced 3D Imaging |
| dc.creator.none.fl_str_mv |
Zunino, Alessandro Garzella, Francesco Trianni, Alberta Saggau, Peter Bianchini, Paolo Diaspro, Alberto Duocastella, Martí |
| author |
Zunino, Alessandro |
| author_facet |
Zunino, Alessandro Garzella, Francesco Trianni, Alberta Saggau, Peter Bianchini, Paolo Diaspro, Alberto Duocastella, Martí |
| author_role |
author |
| author2 |
Garzella, Francesco Trianni, Alberta Saggau, Peter Bianchini, Paolo Diaspro, Alberto Duocastella, Martí |
| author2_role |
author author author author author author |
| dc.subject.none.fl_str_mv |
Microscopis Visualització tridimensional Microscopes Three-dimensional display systems |
| topic |
Microscopis Visualització tridimensional Microscopes Three-dimensional display systems |
| description |
Light-sheet microscopes have become the tool of choice for volumetric imaging of large samples. Based on a wide-field acquisition scheme, they are capable of optical sectioning at diffraction-limited resolution and minimal overall photodamage. Unfortunately, traditional architectures are limited in speed because 3D images are collected by either sample translation or synchronized movement of both light-sheet and detection objective lens. A promising solution avoiding slow mechanical movements is to extend the depth-of-field of the microscope and moving only the light-sheet. However, this normally comes at the cost of losing light and contrast, compromising the signal-to-noise ratio of the images. Here, we propose an innovative technique devoted to restoring the quality of the images, while preserving the speed of extended depth-of-field microscopes. It is based on generating a stack of parallel light-sheets using a pair of orthogonal acousto-optic deflectors, enabling the simultaneous illumination of different sample planes. Given the extended depth-of-field, all such planes appear in focus and can be acquired in a superimposed single frame. By applying a single-step inversion algorithm, we can decode a stack of frames into a volumetric image whose signal-to-noise ratio and contrast are greatly enhanced. We provide a detailed theoretical framework of the method and demonstrate its feasibility with volumetric images of kidney cell spheroids. |
| publishDate |
2021 |
| dc.date.none.fl_str_mv |
2021 2022 2022 2022 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
| format |
article |
| status_str |
publishedVersion |
| dc.identifier.none.fl_str_mv |
https://hdl.handle.net/2445/183314 |
| url |
https://hdl.handle.net/2445/183314 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.relation.none.fl_str_mv |
Reproducció del document publicat a: https://doi.org/10.1021/acsphotonics.1c01401 ACS Photonics, 2021 https://doi.org/10.1021/acsphotonics.1c01401 |
| dc.rights.none.fl_str_mv |
(c) Zunino, Alessandro, et al., 2021 info:eu-repo/semantics/openAccess |
| rights_invalid_str_mv |
(c) Zunino, Alessandro, et al., 2021 |
| eu_rights_str_mv |
openAccess |
| dc.format.none.fl_str_mv |
application/pdf |
| dc.publisher.none.fl_str_mv |
American Chemical Society |
| publisher.none.fl_str_mv |
American Chemical Society |
| dc.source.none.fl_str_mv |
Articles publicats en revistes (Física Aplicada) reponame:Recercat. Dipósit de la Recerca de Catalunya instname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
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Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
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Recercat. Dipósit de la Recerca de Catalunya |
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Recercat. Dipósit de la Recerca de Catalunya |
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