Cargando…

Miniscope3D: optimized single-shot miniature 3D fluorescence microscopy

Miniature fluorescence microscopes are a standard tool in systems biology. However, widefield miniature microscopes capture only 2D information, and modifications that enable 3D capabilities increase the size and weight and have poor resolution outside a narrow depth range. Here, we achieve the 3D c...

Descripción completa

Detalles Bibliográficos
Autores principales: Yanny, Kyrollos, Antipa, Nick, Liberti, William, Dehaeck, Sam, Monakhova, Kristina, Liu, Fanglin Linda, Shen, Konlin, Ng, Ren, Waller, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7532148/
https://www.ncbi.nlm.nih.gov/pubmed/33082940
http://dx.doi.org/10.1038/s41377-020-00403-7
_version_ 1783589864597356544
author Yanny, Kyrollos
Antipa, Nick
Liberti, William
Dehaeck, Sam
Monakhova, Kristina
Liu, Fanglin Linda
Shen, Konlin
Ng, Ren
Waller, Laura
author_facet Yanny, Kyrollos
Antipa, Nick
Liberti, William
Dehaeck, Sam
Monakhova, Kristina
Liu, Fanglin Linda
Shen, Konlin
Ng, Ren
Waller, Laura
author_sort Yanny, Kyrollos
collection PubMed
description Miniature fluorescence microscopes are a standard tool in systems biology. However, widefield miniature microscopes capture only 2D information, and modifications that enable 3D capabilities increase the size and weight and have poor resolution outside a narrow depth range. Here, we achieve the 3D capability by replacing the tube lens of a conventional 2D Miniscope with an optimized multifocal phase mask at the objective’s aperture stop. Placing the phase mask at the aperture stop significantly reduces the size of the device, and varying the focal lengths enables a uniform resolution across a wide depth range. The phase mask encodes the 3D fluorescence intensity into a single 2D measurement, and the 3D volume is recovered by solving a sparsity-constrained inverse problem. We provide methods for designing and fabricating the phase mask and an efficient forward model that accounts for the field-varying aberrations in miniature objectives. We demonstrate a prototype that is 17 mm tall and weighs 2.5 grams, achieving 2.76 μm lateral, and 15 μm axial resolution across most of the 900 × 700 × 390 μm(3) volume at 40 volumes per second. The performance is validated experimentally on resolution targets, dynamic biological samples, and mouse brain tissue. Compared with existing miniature single-shot volume-capture implementations, our system is smaller and lighter and achieves a more than 2× better lateral and axial resolution throughout a 10× larger usable depth range. Our microscope design provides single-shot 3D imaging for applications where a compact platform matters, such as volumetric neural imaging in freely moving animals and 3D motion studies of dynamic samples in incubators and lab-on-a-chip devices.
format Online
Article
Text
id pubmed-7532148
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-75321482020-10-19 Miniscope3D: optimized single-shot miniature 3D fluorescence microscopy Yanny, Kyrollos Antipa, Nick Liberti, William Dehaeck, Sam Monakhova, Kristina Liu, Fanglin Linda Shen, Konlin Ng, Ren Waller, Laura Light Sci Appl Article Miniature fluorescence microscopes are a standard tool in systems biology. However, widefield miniature microscopes capture only 2D information, and modifications that enable 3D capabilities increase the size and weight and have poor resolution outside a narrow depth range. Here, we achieve the 3D capability by replacing the tube lens of a conventional 2D Miniscope with an optimized multifocal phase mask at the objective’s aperture stop. Placing the phase mask at the aperture stop significantly reduces the size of the device, and varying the focal lengths enables a uniform resolution across a wide depth range. The phase mask encodes the 3D fluorescence intensity into a single 2D measurement, and the 3D volume is recovered by solving a sparsity-constrained inverse problem. We provide methods for designing and fabricating the phase mask and an efficient forward model that accounts for the field-varying aberrations in miniature objectives. We demonstrate a prototype that is 17 mm tall and weighs 2.5 grams, achieving 2.76 μm lateral, and 15 μm axial resolution across most of the 900 × 700 × 390 μm(3) volume at 40 volumes per second. The performance is validated experimentally on resolution targets, dynamic biological samples, and mouse brain tissue. Compared with existing miniature single-shot volume-capture implementations, our system is smaller and lighter and achieves a more than 2× better lateral and axial resolution throughout a 10× larger usable depth range. Our microscope design provides single-shot 3D imaging for applications where a compact platform matters, such as volumetric neural imaging in freely moving animals and 3D motion studies of dynamic samples in incubators and lab-on-a-chip devices. Nature Publishing Group UK 2020-10-02 /pmc/articles/PMC7532148/ /pubmed/33082940 http://dx.doi.org/10.1038/s41377-020-00403-7 Text en © The Author(s) 2020, corrected publication 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Yanny, Kyrollos
Antipa, Nick
Liberti, William
Dehaeck, Sam
Monakhova, Kristina
Liu, Fanglin Linda
Shen, Konlin
Ng, Ren
Waller, Laura
Miniscope3D: optimized single-shot miniature 3D fluorescence microscopy
title Miniscope3D: optimized single-shot miniature 3D fluorescence microscopy
title_full Miniscope3D: optimized single-shot miniature 3D fluorescence microscopy
title_fullStr Miniscope3D: optimized single-shot miniature 3D fluorescence microscopy
title_full_unstemmed Miniscope3D: optimized single-shot miniature 3D fluorescence microscopy
title_short Miniscope3D: optimized single-shot miniature 3D fluorescence microscopy
title_sort miniscope3d: optimized single-shot miniature 3d fluorescence microscopy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7532148/
https://www.ncbi.nlm.nih.gov/pubmed/33082940
http://dx.doi.org/10.1038/s41377-020-00403-7
work_keys_str_mv AT yannykyrollos miniscope3doptimizedsingleshotminiature3dfluorescencemicroscopy
AT antipanick miniscope3doptimizedsingleshotminiature3dfluorescencemicroscopy
AT libertiwilliam miniscope3doptimizedsingleshotminiature3dfluorescencemicroscopy
AT dehaecksam miniscope3doptimizedsingleshotminiature3dfluorescencemicroscopy
AT monakhovakristina miniscope3doptimizedsingleshotminiature3dfluorescencemicroscopy
AT liufanglinlinda miniscope3doptimizedsingleshotminiature3dfluorescencemicroscopy
AT shenkonlin miniscope3doptimizedsingleshotminiature3dfluorescencemicroscopy
AT ngren miniscope3doptimizedsingleshotminiature3dfluorescencemicroscopy
AT wallerlaura miniscope3doptimizedsingleshotminiature3dfluorescencemicroscopy