3D tracking of extracellular vesicles by holographic fluorescence imaging

Matz Liebel, Jaime Ortega Arroyo, Vanesa Sanz Beltrán, Johann Osmond, Ala Jo, Hakho Lee, Romain Quidant, Niek F. van Hulst

Research output: Contribution to JournalArticleAcademicpeer-review

Abstract

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.
Original languageEnglish
Article numbereabc2508
JournalScience advances
Volume6
Issue number45
DOIs
Publication statusPublished - 4 Nov 2020
Externally publishedYes

Funding

This research was funded by the European Commission (European Research Council, ERC Advanced Grant 670949-LightNet and ERC Consolidator Grant 647901-QnanoMECA); Ministry of Science, Innovation and Universities (MCIU) Severo Ochoa Programme for Centres of Excellence in R&D (CEX2019-000910-S), FIS2016-80293-R, RTI2018-099957-J-I00 and PGC2018-096875-B-I00; Catalan Agència de Gestió d'Ajuts Universitaris i de Recerca (AGAUR) 2017SGR1369 and 2017SGR1363; Centres de Recerca de Catalunya (CERCA); Fundació Privada Cellex and Fundació Privada Mir-Puig. M.L. and J.O.A. acknowledge financial support from the Marie-Curie International Fellowship, Co-funding of regional, national, and international programmes (COFUND). H.L. was partly supported by NIH grants (R01CA229777, U01CA233360, and R21DA049577) and DoD awards (W81XWH-19-1-0199 and W81XWH-19-1-0194).

FundersFunder number
Fundació Privada Cellex and Fundació Privada Mir-Puig
National Institutes of HealthU01CA233360, R21DA049577
U.S. Department of DefenseW81XWH-19-1-0199, W81XWH-19-1-0194
National Cancer InstituteR01CA229777
Ministerio de Ciencia, Innovación y UniversidadesPGC2018-096875-B-I00, RTI2018-099957-J-I00, CEX2019-000910-S, FIS2016-80293-R
European Commission
European Research Council670949-LightNet, 647901-QnanoMECA
Agència de Gestió d'Ajuts Universitaris i de Recerca2017SGR1363, 2017SGR1369

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