Analysis of intracellular protein dynamics in living zebrafish embryos using light-sheet fluorescence single-molecule microscopy

被引:3
作者
Bernardello, Matteo [1 ]
Gora, Radoslaw J. [2 ]
Van Hage, Patrick [2 ]
Castro-olvera, Gustavo [1 ]
Gualda, Emilio J. [1 ]
Schaaf, Marcel J. M. [2 ]
Loza-alvarez, Pablo [1 ]
机构
[1] Barcelona Inst Sci & Technol, ICFO Inst Ciencies Foton, Castelldefels 08860, Spain
[2] Leiden Univ, Inst Biol, Leiden, Netherlands
基金
欧盟地平线“2020”;
关键词
YOLK SYNCYTIAL LAYER; PARTICLE TRACKING; CELLS; BINDING; SYSTEM;
D O I
10.1364/BOE.435103
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Single-molecule microscopy techniques have emerged as useful tools to image individual molecules and analyze their dynamics inside cells, but their application has mostly been restricted to cell cultures. Here, a light-sheet fluorescence microscopy setup is presented for imaging individual proteins inside living zebrafish embryos. The optical configuration makes this design accessible to many laboratories and a dedicated sample-mounting system ensures sample viability and mounting flexibility. Using this setup, we have analyzed the dynamics of individual glucocorticoid receptors, which demonstrates that this approach creates multiple possibilities for the analysis of intracellular protein dynamics in intact living organisms. (c) 2021 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
引用
收藏
页码:6205 / 6227
页数:23
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