A set of monomeric near-infrared fluorescent proteins for multicolor imaging across scales

被引:117
|
作者
Matlashov, Mikhail E. [1 ,2 ]
Shcherbakova, Daria M. [1 ,2 ]
Alvelid, Jonatan [3 ,4 ]
Baloban, Mikhail [1 ,2 ]
Pennacchietti, Francesca [3 ,4 ]
Shemetov, Anton A. [1 ,2 ]
Testa, Ilaria [3 ,4 ]
Verkhusha, Vladislav V. [1 ,2 ,5 ]
机构
[1] Albert Einstein Coll Med, Dept Anat & Struct Biol, Bronx, NY 10461 USA
[2] Albert Einstein Coll Med, Gruss Lipper Biophoton Ctr, Bronx, NY 10461 USA
[3] KTH Royal Inst Technol, Dept Appl Phys, Stockholm, Sweden
[4] KTH Royal Inst Technol, Sci Life Lab, Stockholm, Sweden
[5] Univ Helsinki, Fac Med, Medicum, Helsinki 00029, Finland
基金
美国国家卫生研究院; 瑞典研究理事会;
关键词
MICROSCOPY; INSIGHTS; BRIGHT; LIGHT; KNOT;
D O I
10.1038/s41467-019-13897-6
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
Bright monomeric near-infrared (NIR) fluorescent proteins (FPs) are in high demand as protein tags for multicolor microscopy and in vivo imaging. Here we apply rational design to engineer a complete set of monomeric NIR FPs, which are the brightest genetically encoded NIR probes. We demonstrate that the enhanced miRFP series of NIR FPs, which combine high effective brightness in mammalian cells and monomeric state, perform well in both nanometer-scale imaging with diffraction unlimited stimulated emission depletion (STED) microscopy and centimeter-scale imaging in mice. In STED we achieve -40nm resolution in live cells. In living mice we detect -10(5) fluorescent cells in deep tissues. Using spectrally distinct monomeric NIR FP variants, we perform two-color live-cell STED microscopy and two-color imaging in vivo. Having emission peaks from 670nm to 720nm, the next generation of miRFPs should become versatile NIR probes for multiplexed imaging across spatial scales in different modalities.
引用
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页数:12
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