Engineering of mCherry variants with long Stokes shift, red-shifted fluorescence, and low cytotoxicity

被引:49
|
作者
Shen, Yi [1 ]
Chen, Yingche [1 ]
Wu, Jiahui [1 ]
Shaner, Nathan C. [2 ]
Campbell, Robert E. [1 ]
机构
[1] Univ Alberta, Dept Chem, Edmonton, AB, Canada
[2] Scintillon Inst, Dept Photobiol & Bioimaging, San Diego, CA USA
来源
PLOS ONE | 2017年 / 12卷 / 02期
基金
加拿大自然科学与工程研究理事会;
关键词
MONOMERIC RED; CORRELATION SPECTROSCOPY; CRYSTAL-STRUCTURE; CA2+ INDICATORS; IN-VIVO; PROTEIN; GREEN; BRIGHT; ORANGE; AEQUOREA;
D O I
10.1371/journal.pone.0171257
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
MCherry, the Discosoma sp. mushroom coral-derived monomeric red fluorescent protein (RFP), is a commonly used genetically encoded fluorophore for live cell fluorescence imaging. We have used a combination of protein design and directed evolution to develop mCherry variants with low cytotoxicity to Escherichia coli and altered excitation and emission profiles. These efforts ultimately led to a long Stokes shift (LSS)-mCherry variant (lambda(ex) = 460 nm and lambda(em) = 610 nm) and a red-shifted (RDS)-mCherry variant (lambda(ex) = 600 nm and lambda(em) = 630 nm). These new RFPs provide insight into the influence of the chromophore environment on mCherry's fluorescence properties, and may serve as templates for the future development of fluorescent probes for live cell imaging.
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页数:14
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