Autonomous bioluminescence imaging of single mammalian cells with the bacterial bioluminescence system

被引:42
作者
Gregor, Carola [1 ]
Pape, Jasmin K. [1 ]
Gwosch, Klaus C. [1 ]
Gilat, Tanja [1 ]
Sahl, Steffen J. [1 ]
Hell, Stefan W. [1 ,2 ]
机构
[1] Max Planck Inst Biophys Chem, Dept NanoBiophoton, D-37077 Gottingen, Germany
[2] Max Planck Inst Med Res, Dept Opt Nanoscopy, D-69120 Heidelberg, Germany
关键词
bioluminescence; luciferase; lux; microscopy; FATTY-ACIDS; LUCIFERASE; EXPRESSION; GENE; LUX;
D O I
10.1073/pnas.1913616116
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
Bioluminescence-based imaging of living cells has become an important tool in biological and medical research. However, many bioluminescence imaging applications are limited by the requirement of an externally provided luciferin substrate and the low bioluminescence signal which restricts the sensitivity and spatiotemporal resolution. The bacterial bioluminescence system is fully genetically encodable and hence produces autonomous bioluminescence without an external luciferin, but its brightness in cell types other than bacteria has, so far, not been sufficient for imaging single cells. We coexpressed codon-optimized forms of the bacterial luxCDABE and frp genes from multiple plasmids in different mammalian cell lines. Our approach produces high luminescence levels that are comparable to firefly luciferase, thus enabling autonomous bioluminescence microscopy of mammalian cells.
引用
收藏
页码:26491 / 26496
页数:6
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