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Label-free imaging and biomarker analysis of exosomes with plasmonic scattering microscopy
Exosome analysis is a promising tool for clinical and biological research applications. However, detection and biomarker quantification of exosomes is technically challenging because they are small and highly heterogeneous. Here, we report an optical approach for imaging exosomes and quantifying the...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9645376/ https://www.ncbi.nlm.nih.gov/pubmed/36519046 http://dx.doi.org/10.1039/d2sc05191e |
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author | Zhang, Pengfei Jiang, Jiapei Zhou, Xinyu Kolay, Jayeeta Wang, Rui Wan, Zijian Wang, Shaopeng |
author_facet | Zhang, Pengfei Jiang, Jiapei Zhou, Xinyu Kolay, Jayeeta Wang, Rui Wan, Zijian Wang, Shaopeng |
author_sort | Zhang, Pengfei |
collection | PubMed |
description | Exosome analysis is a promising tool for clinical and biological research applications. However, detection and biomarker quantification of exosomes is technically challenging because they are small and highly heterogeneous. Here, we report an optical approach for imaging exosomes and quantifying their protein markers without labels using plasmonic scattering microscopy (PSM). PSM can provide improved spatial resolution and distortion-free image compared to conventional surface plasmon resonance (SPR) microscopy, with the signal-to-noise ratio similar to objective coupled surface plasmon resonance (SPR) microscopy, and millimeter-scale field of view as a prism-coupled SPR system, thus allowing exosome size distribution analysis with high throughput. In addition, PSM retains the high specificity and surface sensitivity of the SPR sensors and thus allows selection of exosomes from extracellular vesicles with antibody-modified sensor surfaces and in situ analyzing binding kinetics between antibody and the surface protein biomarkers on the captured exosomes. Finally, the PSM can be easily constructed on a popular prism-coupled SPR system with commercially available components. Thus, it may provide an economical and powerful tool for clinical exosome analysis and exploration of fundamental issues such as exosome biomarker binding properties. |
format | Online Article Text |
id | pubmed-9645376 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-96453762022-12-13 Label-free imaging and biomarker analysis of exosomes with plasmonic scattering microscopy Zhang, Pengfei Jiang, Jiapei Zhou, Xinyu Kolay, Jayeeta Wang, Rui Wan, Zijian Wang, Shaopeng Chem Sci Chemistry Exosome analysis is a promising tool for clinical and biological research applications. However, detection and biomarker quantification of exosomes is technically challenging because they are small and highly heterogeneous. Here, we report an optical approach for imaging exosomes and quantifying their protein markers without labels using plasmonic scattering microscopy (PSM). PSM can provide improved spatial resolution and distortion-free image compared to conventional surface plasmon resonance (SPR) microscopy, with the signal-to-noise ratio similar to objective coupled surface plasmon resonance (SPR) microscopy, and millimeter-scale field of view as a prism-coupled SPR system, thus allowing exosome size distribution analysis with high throughput. In addition, PSM retains the high specificity and surface sensitivity of the SPR sensors and thus allows selection of exosomes from extracellular vesicles with antibody-modified sensor surfaces and in situ analyzing binding kinetics between antibody and the surface protein biomarkers on the captured exosomes. Finally, the PSM can be easily constructed on a popular prism-coupled SPR system with commercially available components. Thus, it may provide an economical and powerful tool for clinical exosome analysis and exploration of fundamental issues such as exosome biomarker binding properties. The Royal Society of Chemistry 2022-10-12 /pmc/articles/PMC9645376/ /pubmed/36519046 http://dx.doi.org/10.1039/d2sc05191e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Zhang, Pengfei Jiang, Jiapei Zhou, Xinyu Kolay, Jayeeta Wang, Rui Wan, Zijian Wang, Shaopeng Label-free imaging and biomarker analysis of exosomes with plasmonic scattering microscopy |
title | Label-free imaging and biomarker analysis of exosomes with plasmonic scattering microscopy |
title_full | Label-free imaging and biomarker analysis of exosomes with plasmonic scattering microscopy |
title_fullStr | Label-free imaging and biomarker analysis of exosomes with plasmonic scattering microscopy |
title_full_unstemmed | Label-free imaging and biomarker analysis of exosomes with plasmonic scattering microscopy |
title_short | Label-free imaging and biomarker analysis of exosomes with plasmonic scattering microscopy |
title_sort | label-free imaging and biomarker analysis of exosomes with plasmonic scattering microscopy |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9645376/ https://www.ncbi.nlm.nih.gov/pubmed/36519046 http://dx.doi.org/10.1039/d2sc05191e |
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