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Parallel Fourier ptychographic microscopy for high-throughput screening with 96 cameras (96 Eyes)
We report the implementation of a parallel microscopy system (96 Eyes) that is capable of simultaneous imaging of all wells on a 96-well plate. The optical system consists of 96 microscopy units, where each unit is made out of a four element objective, made through a molded injection process, and a...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6668459/ https://www.ncbi.nlm.nih.gov/pubmed/31366957 http://dx.doi.org/10.1038/s41598-019-47146-z |
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author | Chan, Antony C. S. Kim, Jinho Pan, An Xu, Han Nojima, Dana Hale, Christopher Wang, Songli Yang, Changhuei |
author_facet | Chan, Antony C. S. Kim, Jinho Pan, An Xu, Han Nojima, Dana Hale, Christopher Wang, Songli Yang, Changhuei |
author_sort | Chan, Antony C. S. |
collection | PubMed |
description | We report the implementation of a parallel microscopy system (96 Eyes) that is capable of simultaneous imaging of all wells on a 96-well plate. The optical system consists of 96 microscopy units, where each unit is made out of a four element objective, made through a molded injection process, and a low cost CMOS camera chip. By illuminating the sample with angle varying light and applying Fourier Ptychography, we can improve the effective brightfield imaging numerical aperture of the objectives from 0.23 to 0.3, and extend the depth of field from ±5 μm to ±15 μm. The use of Fourier Ptychography additionally allows us to computationally correct the objectives’ aberrations out of the rendered images, and provides us with the ability to render phase images. The 96 Eyes acquires raw data at a rate of 0.7 frame per second (all wells) and the data are processed with 4 cores of graphical processing units (GPUs; GK210, Nvidia Tesla K80, USA). The system is also capable of fluorescence imaging (excitation = 465 nm, emission = 510 nm) at the native resolution of the objectives. We demonstrate the capability of this system by imaging S1P(1)-eGFP-Human bone osteosarcoma epithelial (U2OS) cells. |
format | Online Article Text |
id | pubmed-6668459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66684592019-08-06 Parallel Fourier ptychographic microscopy for high-throughput screening with 96 cameras (96 Eyes) Chan, Antony C. S. Kim, Jinho Pan, An Xu, Han Nojima, Dana Hale, Christopher Wang, Songli Yang, Changhuei Sci Rep Article We report the implementation of a parallel microscopy system (96 Eyes) that is capable of simultaneous imaging of all wells on a 96-well plate. The optical system consists of 96 microscopy units, where each unit is made out of a four element objective, made through a molded injection process, and a low cost CMOS camera chip. By illuminating the sample with angle varying light and applying Fourier Ptychography, we can improve the effective brightfield imaging numerical aperture of the objectives from 0.23 to 0.3, and extend the depth of field from ±5 μm to ±15 μm. The use of Fourier Ptychography additionally allows us to computationally correct the objectives’ aberrations out of the rendered images, and provides us with the ability to render phase images. The 96 Eyes acquires raw data at a rate of 0.7 frame per second (all wells) and the data are processed with 4 cores of graphical processing units (GPUs; GK210, Nvidia Tesla K80, USA). The system is also capable of fluorescence imaging (excitation = 465 nm, emission = 510 nm) at the native resolution of the objectives. We demonstrate the capability of this system by imaging S1P(1)-eGFP-Human bone osteosarcoma epithelial (U2OS) cells. Nature Publishing Group UK 2019-07-31 /pmc/articles/PMC6668459/ /pubmed/31366957 http://dx.doi.org/10.1038/s41598-019-47146-z Text en © The Author(s) 2019 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/. |
spellingShingle | Article Chan, Antony C. S. Kim, Jinho Pan, An Xu, Han Nojima, Dana Hale, Christopher Wang, Songli Yang, Changhuei Parallel Fourier ptychographic microscopy for high-throughput screening with 96 cameras (96 Eyes) |
title | Parallel Fourier ptychographic microscopy for high-throughput screening with 96 cameras (96 Eyes) |
title_full | Parallel Fourier ptychographic microscopy for high-throughput screening with 96 cameras (96 Eyes) |
title_fullStr | Parallel Fourier ptychographic microscopy for high-throughput screening with 96 cameras (96 Eyes) |
title_full_unstemmed | Parallel Fourier ptychographic microscopy for high-throughput screening with 96 cameras (96 Eyes) |
title_short | Parallel Fourier ptychographic microscopy for high-throughput screening with 96 cameras (96 Eyes) |
title_sort | parallel fourier ptychographic microscopy for high-throughput screening with 96 cameras (96 eyes) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6668459/ https://www.ncbi.nlm.nih.gov/pubmed/31366957 http://dx.doi.org/10.1038/s41598-019-47146-z |
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