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High-throughput spatiotemporal monitoring of single-cell secretions via plasmonic microwell arrays
Methods for the analysis of cell secretions at the single-cell level only provide semiquantitative endpoint readouts. Here we describe a microwell array for the real-time spatiotemporal monitoring of extracellular secretions from hundreds of single cells in parallel. The microwell array incorporates...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10365996/ https://www.ncbi.nlm.nih.gov/pubmed/37012313 http://dx.doi.org/10.1038/s41551-023-01017-1 |
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author | Ansaryan, Saeid Liu, Yen-Cheng Li, Xiaokang Economou, Augoustina Maria Eberhardt, Christiane Sigrid Jandus, Camilla Altug, Hatice |
author_facet | Ansaryan, Saeid Liu, Yen-Cheng Li, Xiaokang Economou, Augoustina Maria Eberhardt, Christiane Sigrid Jandus, Camilla Altug, Hatice |
author_sort | Ansaryan, Saeid |
collection | PubMed |
description | Methods for the analysis of cell secretions at the single-cell level only provide semiquantitative endpoint readouts. Here we describe a microwell array for the real-time spatiotemporal monitoring of extracellular secretions from hundreds of single cells in parallel. The microwell array incorporates a gold substrate with arrays of nanometric holes functionalized with receptors for a specific analyte, and is illuminated with light spectrally overlapping with the device’s spectrum of extraordinary optical transmission. Spectral shifts in surface plasmon resonance resulting from analyte–receptor bindings around a secreting cell are recorded by a camera as variations in the intensity of the transmitted light while machine-learning-assisted cell tracking eliminates the influence of cell movements. We used the microwell array to characterize the antibody-secretion profiles of hybridoma cells and of a rare subset of antibody-secreting cells sorted from human donor peripheral blood mononuclear cells. High-throughput measurements of spatiotemporal secretory profiles at the single-cell level will aid the study of the physiological mechanisms governing protein secretion. |
format | Online Article Text |
id | pubmed-10365996 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103659962023-07-26 High-throughput spatiotemporal monitoring of single-cell secretions via plasmonic microwell arrays Ansaryan, Saeid Liu, Yen-Cheng Li, Xiaokang Economou, Augoustina Maria Eberhardt, Christiane Sigrid Jandus, Camilla Altug, Hatice Nat Biomed Eng Article Methods for the analysis of cell secretions at the single-cell level only provide semiquantitative endpoint readouts. Here we describe a microwell array for the real-time spatiotemporal monitoring of extracellular secretions from hundreds of single cells in parallel. The microwell array incorporates a gold substrate with arrays of nanometric holes functionalized with receptors for a specific analyte, and is illuminated with light spectrally overlapping with the device’s spectrum of extraordinary optical transmission. Spectral shifts in surface plasmon resonance resulting from analyte–receptor bindings around a secreting cell are recorded by a camera as variations in the intensity of the transmitted light while machine-learning-assisted cell tracking eliminates the influence of cell movements. We used the microwell array to characterize the antibody-secretion profiles of hybridoma cells and of a rare subset of antibody-secreting cells sorted from human donor peripheral blood mononuclear cells. High-throughput measurements of spatiotemporal secretory profiles at the single-cell level will aid the study of the physiological mechanisms governing protein secretion. Nature Publishing Group UK 2023-04-03 2023 /pmc/articles/PMC10365996/ /pubmed/37012313 http://dx.doi.org/10.1038/s41551-023-01017-1 Text en © The Author(s) 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 Ansaryan, Saeid Liu, Yen-Cheng Li, Xiaokang Economou, Augoustina Maria Eberhardt, Christiane Sigrid Jandus, Camilla Altug, Hatice High-throughput spatiotemporal monitoring of single-cell secretions via plasmonic microwell arrays |
title | High-throughput spatiotemporal monitoring of single-cell secretions via plasmonic microwell arrays |
title_full | High-throughput spatiotemporal monitoring of single-cell secretions via plasmonic microwell arrays |
title_fullStr | High-throughput spatiotemporal monitoring of single-cell secretions via plasmonic microwell arrays |
title_full_unstemmed | High-throughput spatiotemporal monitoring of single-cell secretions via plasmonic microwell arrays |
title_short | High-throughput spatiotemporal monitoring of single-cell secretions via plasmonic microwell arrays |
title_sort | high-throughput spatiotemporal monitoring of single-cell secretions via plasmonic microwell arrays |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10365996/ https://www.ncbi.nlm.nih.gov/pubmed/37012313 http://dx.doi.org/10.1038/s41551-023-01017-1 |
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