Flow cytometry based-FRET: basics, novel developments and future perspectives

被引:13
|
作者
Lim, JiaWen [1 ]
Petersen, Moritz [1 ]
Bunz, Maximilian [1 ]
Simon, Claudia [1 ]
Schindler, Michael [1 ]
机构
[1] Univ Hosp Tubingen, Inst Med Virol & Epidemiol Viral Dis, Tubingen, Germany
关键词
FACS; Forster resonance energy transfer; FLIM; Fluorescence proteins; Molecular interactions; Protein interactions; RESONANCE ENERGY-TRANSFER; YELLOW FLUORESCENT PROTEIN; MOLECULAR-INTERACTIONS; MICROSCOPY; CELLS; MATURATION; GREEN; RED;
D O I
10.1007/s00018-022-04232-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Forster resonance energy transfer (FRET) is a widespread technology used to analyze and quantify protein interactions in multiple settings. While FRET is traditionally measured by microscopy, flow cytometry based-FRET is becoming popular within the last decade and more commonly used. Flow cytometry based-FRET offers the possibility to assess FRET in a short time-frame in a high number of cells thereby allowing stringent and statistically robust quantification of FRET in multiple samples. Furthermore, established, simple and easy to implement gating strategies facilitate the adaptation of flow cytometry based-FRET measurements to most common flow cytometers. We here summarize the basics of flow cytometry based-FRET, highlight recent novel developments in this field and emphasize on exciting future perspectives.
引用
收藏
页数:12
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