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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...

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Autores principales: Liebel, Matz, Ortega Arroyo, Jaime, Beltrán, Vanesa Sanz, Osmond, Johann, Jo, Ala, Lee, Hakho, Quidant, Romain, van Hulst, Niek F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
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.
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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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