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Cellular lensing and near infrared fluorescent nanosensor arrays to enable chemical efflux cytometry
Nanosensors have proven to be powerful tools to monitor single cells, achieving spatiotemporal precision even at molecular level. However, there has not been way of extending this approach to statistically relevant numbers of living cells. Herein, we design and fabricate nanosensor array in microflu...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8149711/ https://www.ncbi.nlm.nih.gov/pubmed/34035262 http://dx.doi.org/10.1038/s41467-021-23416-1 |
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author | Cho, Soo-Yeon Gong, Xun Koman, Volodymyr B. Kuehne, Matthias Moon, Sun Jin Son, Manki Lew, Tedrick Thomas Salim Gordiichuk, Pavlo Jin, Xiaojia Sikes, Hadley D. Strano, Michael S. |
author_facet | Cho, Soo-Yeon Gong, Xun Koman, Volodymyr B. Kuehne, Matthias Moon, Sun Jin Son, Manki Lew, Tedrick Thomas Salim Gordiichuk, Pavlo Jin, Xiaojia Sikes, Hadley D. Strano, Michael S. |
author_sort | Cho, Soo-Yeon |
collection | PubMed |
description | Nanosensors have proven to be powerful tools to monitor single cells, achieving spatiotemporal precision even at molecular level. However, there has not been way of extending this approach to statistically relevant numbers of living cells. Herein, we design and fabricate nanosensor array in microfluidics that addresses this limitation, creating a Nanosensor Chemical Cytometry (NCC). nIR fluorescent carbon nanotube array is integrated along microfluidic channel through which flowing cells is guided. We can utilize the flowing cell itself as highly informative Gaussian lenses projecting nIR profiles and extract rich information. This unique biophotonic waveguide allows for quantified cross-correlation of biomolecular information with various physical properties and creates label-free chemical cytometer for cellular heterogeneity measurement. As an example, the NCC can profile the immune heterogeneities of human monocyte populations at attomolar sensitivity in completely non-destructive and real-time manner with rate of ~600 cells/hr, highest range demonstrated to date for state-of-the-art chemical cytometry. |
format | Online Article Text |
id | pubmed-8149711 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81497112021-06-01 Cellular lensing and near infrared fluorescent nanosensor arrays to enable chemical efflux cytometry Cho, Soo-Yeon Gong, Xun Koman, Volodymyr B. Kuehne, Matthias Moon, Sun Jin Son, Manki Lew, Tedrick Thomas Salim Gordiichuk, Pavlo Jin, Xiaojia Sikes, Hadley D. Strano, Michael S. Nat Commun Article Nanosensors have proven to be powerful tools to monitor single cells, achieving spatiotemporal precision even at molecular level. However, there has not been way of extending this approach to statistically relevant numbers of living cells. Herein, we design and fabricate nanosensor array in microfluidics that addresses this limitation, creating a Nanosensor Chemical Cytometry (NCC). nIR fluorescent carbon nanotube array is integrated along microfluidic channel through which flowing cells is guided. We can utilize the flowing cell itself as highly informative Gaussian lenses projecting nIR profiles and extract rich information. This unique biophotonic waveguide allows for quantified cross-correlation of biomolecular information with various physical properties and creates label-free chemical cytometer for cellular heterogeneity measurement. As an example, the NCC can profile the immune heterogeneities of human monocyte populations at attomolar sensitivity in completely non-destructive and real-time manner with rate of ~600 cells/hr, highest range demonstrated to date for state-of-the-art chemical cytometry. Nature Publishing Group UK 2021-05-25 /pmc/articles/PMC8149711/ /pubmed/34035262 http://dx.doi.org/10.1038/s41467-021-23416-1 Text en © The Author(s) 2021 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 Cho, Soo-Yeon Gong, Xun Koman, Volodymyr B. Kuehne, Matthias Moon, Sun Jin Son, Manki Lew, Tedrick Thomas Salim Gordiichuk, Pavlo Jin, Xiaojia Sikes, Hadley D. Strano, Michael S. Cellular lensing and near infrared fluorescent nanosensor arrays to enable chemical efflux cytometry |
title | Cellular lensing and near infrared fluorescent nanosensor arrays to enable chemical efflux cytometry |
title_full | Cellular lensing and near infrared fluorescent nanosensor arrays to enable chemical efflux cytometry |
title_fullStr | Cellular lensing and near infrared fluorescent nanosensor arrays to enable chemical efflux cytometry |
title_full_unstemmed | Cellular lensing and near infrared fluorescent nanosensor arrays to enable chemical efflux cytometry |
title_short | Cellular lensing and near infrared fluorescent nanosensor arrays to enable chemical efflux cytometry |
title_sort | cellular lensing and near infrared fluorescent nanosensor arrays to enable chemical efflux cytometry |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8149711/ https://www.ncbi.nlm.nih.gov/pubmed/34035262 http://dx.doi.org/10.1038/s41467-021-23416-1 |
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