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3D tracking of extracellular vesicles by holographic fluorescence imaging
Fluorescence microscopy is the method of choice in biology for its molecular specificity and super-resolution capabilities. However, it is limited to a narrow z range around one observation plane. Here, we report an imaging approach that recovers the full electric field of fluorescent light with sin...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7673696/ https://www.ncbi.nlm.nih.gov/pubmed/33148645 http://dx.doi.org/10.1126/sciadv.abc2508 |
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author | Liebel, Matz Ortega Arroyo, Jaime Beltrán, Vanesa Sanz Osmond, Johann Jo, Ala Lee, Hakho Quidant, Romain van Hulst, Niek F. |
author_facet | Liebel, Matz Ortega Arroyo, Jaime Beltrán, Vanesa Sanz Osmond, Johann Jo, Ala Lee, Hakho Quidant, Romain van Hulst, Niek F. |
author_sort | Liebel, Matz |
collection | PubMed |
description | Fluorescence microscopy is the method of choice in biology for its molecular specificity and super-resolution capabilities. However, it is limited to a narrow z range around one observation plane. Here, we report an imaging approach that recovers the full electric field of fluorescent light with single-molecule sensitivity. We expand the principle of digital holography to fast fluorescent detection by eliminating the need for phase cycling and enable three-dimensional (3D) tracking of individual nanoparticles with an in-plane resolution of 15 nm and a z-range of 8 mm. As a proof-of-concept biological application, we image the 3D motion of extracellular vesicles (EVs) inside live cells. At short time scales (<4 s), we resolve near-isotropic 3D diffusion and directional transport. For longer lag times, we observe a transition toward anisotropic motion with the EVs being transported over long distances in the axial plane while being confined in the horizontal dimension. |
format | Online Article Text |
id | pubmed-7673696 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-76736962020-11-24 3D tracking of extracellular vesicles by holographic fluorescence imaging Liebel, Matz Ortega Arroyo, Jaime Beltrán, Vanesa Sanz Osmond, Johann Jo, Ala Lee, Hakho Quidant, Romain van Hulst, Niek F. Sci Adv Research Articles Fluorescence microscopy is the method of choice in biology for its molecular specificity and super-resolution capabilities. However, it is limited to a narrow z range around one observation plane. Here, we report an imaging approach that recovers the full electric field of fluorescent light with single-molecule sensitivity. We expand the principle of digital holography to fast fluorescent detection by eliminating the need for phase cycling and enable three-dimensional (3D) tracking of individual nanoparticles with an in-plane resolution of 15 nm and a z-range of 8 mm. As a proof-of-concept biological application, we image the 3D motion of extracellular vesicles (EVs) inside live cells. At short time scales (<4 s), we resolve near-isotropic 3D diffusion and directional transport. For longer lag times, we observe a transition toward anisotropic motion with the EVs being transported over long distances in the axial plane while being confined in the horizontal dimension. American Association for the Advancement of Science 2020-11-04 /pmc/articles/PMC7673696/ /pubmed/33148645 http://dx.doi.org/10.1126/sciadv.abc2508 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Liebel, Matz Ortega Arroyo, Jaime Beltrán, Vanesa Sanz Osmond, Johann Jo, Ala Lee, Hakho Quidant, Romain van Hulst, Niek F. 3D tracking of extracellular vesicles by holographic fluorescence imaging |
title | 3D tracking of extracellular vesicles by holographic fluorescence imaging |
title_full | 3D tracking of extracellular vesicles by holographic fluorescence imaging |
title_fullStr | 3D tracking of extracellular vesicles by holographic fluorescence imaging |
title_full_unstemmed | 3D tracking of extracellular vesicles by holographic fluorescence imaging |
title_short | 3D tracking of extracellular vesicles by holographic fluorescence imaging |
title_sort | 3d tracking of extracellular vesicles by holographic fluorescence imaging |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7673696/ https://www.ncbi.nlm.nih.gov/pubmed/33148645 http://dx.doi.org/10.1126/sciadv.abc2508 |
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