Near-infrared co-illumination of fluorescent proteins reduces photobleaching and phototoxicity

被引:10
|
作者
Ludvikova, Lucie [1 ]
Simon, Emma [1 ]
Deygas, Mathieu [2 ,3 ]
Panier, Thomas [4 ]
Plamont, Marie-Aude [1 ]
Ollion, Jean [5 ]
Tebo, Alison [1 ]
Piel, Matthieu [2 ,3 ]
Jullien, Ludovic [1 ]
Robert, Lydia [4 ,6 ]
Le Saux, Thomas [1 ]
Espagne, Agathe [1 ]
机构
[1] Sorbonne Univ, PSL Univ, CNRS, Ecole Normale Super,Dept Chim,PASTEUR, Paris, France
[2] Paris Sci & Lettres PSL Res Univ, Inst Curie, CNRS, Paris, France
[3] PSL Res Univ, Inst Pierre Gilles Gennes, Paris, France
[4] Sorbonne Univ, Inst Biol Paris Seine IBPS, CNRS, Lab Jean Perrin LJP, Paris, France
[5] SABILab, Die, France
[6] Univ Paris Saclay, Micalis Inst, INRAE, AgroParisTech, Jouy En Josas, France
关键词
STATE; TIME; MICROSCOPY; MECHANISM; TRACKING; GFP;
D O I
10.1038/s41587-023-01893-7
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Here we present a method to reduce the photobleaching of fluorescent proteins and the associated phototoxicity. It exploits a photophysical process known as reverse intersystem crossing, which we induce by near-infrared co-illumination during fluorophore excitation. This dual illumination method reduces photobleaching effects 1.5-9.2-fold, can be easily implemented on commercial microscopes and is effective in eukaryotic and prokaryotic cells with a wide range of fluorescent proteins. A dual illumination method reduces photobleaching for green and yellow fluorescent proteins.
引用
收藏
页码:872 / +
页数:12
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