Monomeric Garnet, a far-red fluorescent protein for live-cell STED imaging

被引:37
作者
Hense, Anika [1 ]
Prunsche, Benedikt [1 ]
Gao, Peng [1 ,2 ]
Ishitsuka, Yuji [1 ]
Nienhaus, Karin [1 ]
Nienhaus, G. Ulrich [1 ,2 ,3 ,4 ]
机构
[1] Karlsruhe Inst Technol, Inst Appl Phys, D-76131 Karlsruhe, Germany
[2] Karlsruhe Inst Technol, Inst Nanotechnol, D-76344 Eggenstein Leopoldshafen, Germany
[3] Karlsruhe Inst Technol, Inst Toxicol & Genet, D-76344 Eggenstein Leopoldshafen, Germany
[4] Univ Illinois, Dept Phys, Urbana, IL 61801 USA
关键词
MICROSCOPY; VARIANTS; MARKER; ISOMERIZATION;
D O I
10.1038/srep18006
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The advancement of far-red emitting variants of the green fluorescent protein (GFP) is crucially important for imaging live cells, tissues and organisms. Despite notable efforts, far-red marker proteins still need further optimization to match the performance of their green counterparts. Here we present mGarnet, a robust monomeric marker protein with far-red fluorescence peaking at 670 nm. Thanks to its large extinction coefficient of 95,000 M(-1)cm(-1), mGarnet can be efficiently excited with 640-nm light on the red edge of its 598-nm excitation band. A large Stokes shift allows essentially the entire fluorescence emission to be collected even with 640-nm excitation, counterbalancing the lower fluorescence quantum yield of mGarnet, 9.1%, that is typical of far-red FPs. We demonstrate an excellent performance as a live-cell fusion marker in STED microscopy, using 640 nm excitation and 780 nm depletion wavelengths.
引用
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页数:10
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