Studying molecular interactions in the intact organism: fluorescence correlation spectroscopy in the living zebrafish embryo

被引:13
作者
Dawes, Michael L. [1 ]
Soeller, Christian [2 ]
Scholpp, Steffen [1 ]
机构
[1] Univ Exeter, Living Syst Inst, Sch Biosci, Coll Life & Environm Sci, Exeter EX4 4QD, Devon, England
[2] Univ Exeter, Living Syst Inst, Coll Engn Math & Phys Sci, Exeter EX4 4QD, Devon, England
基金
英国生物技术与生命科学研究理事会;
关键词
Microscopy; Protein-protein interactions; Fluorescent correlation spectroscopy (FCS); Zebrafish; CROSS-CORRELATION SPECTROSCOPY; RECEPTOR-LIGAND INTERACTIONS; LONG-RANGE; IN-VIVO; SCANNING FCS; WNT PROTEINS; EXPRESSION; DIFFUSION; ACTIVATION; TRANSPORT;
D O I
10.1007/s00418-020-01930-5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cell behaviour and function is determined through the interactions of a multitude of molecules working in concert. To observe these molecular dynamics, biophysical studies have been developed that track single interactions. Fluorescence correlation spectroscopy (FCS) is an optical biophysical technique that non-invasively resolves single molecules through recording the signal intensity at the femtolitre scale. However, recording the behaviour of these biomolecules using in vitro-based assays often fails to recapitulate the full range of variables in vivo that directly confer dynamics. Therefore, there has been an increasing interest in observing the state of these biomolecules within living organisms such as the zebrafishDanio rerio. In this review, we explore the advancements of FCS within the zebrafish and compare and contrast these findings to those found in vitro.
引用
收藏
页码:507 / 519
页数:13
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