3D tracking of extracellular vesicles by holographic fluorescence imaging

被引:0
|
作者
Liebel M. [1 ]
Arroyo J.O. [1 ]
Beltrán V.S. [1 ]
Osmond J. [1 ]
Jo A. [2 ,3 ]
Lee H. [2 ,3 ]
Quidant R. [1 ,4 ]
van Hulst N.F. [1 ,4 ]
机构
[1] ICFO-Institut de Ciencies Fotoniques, Barcelona Institute of Science and Technology, Castelldefels, Barcelona
[2] Center for Systems Biology, Massachusetts General Hospital, Boston, 02114, MA
[3] Department of Radiology, Massachusetts General Hospital, Boston, 02114, MA
[4] ICREA-Institució Catalana de Recerca i Estudis Avançats, Barcelona
来源
Science Advances | 2020年 / 6卷 / 45期
基金
美国国家卫生研究院; 欧洲研究理事会;
关键词
Electric fields - Holography - Fluorescence imaging;
D O I
10.1126/SCIADV.ABC2508
中图分类号
学科分类号
摘要
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. 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).
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