Luciferase complementation for cellular assays beyond protein-protein interactions

被引:0
|
作者
Kawamura, Genki [1 ]
Ozawa, Takeaki [1 ]
机构
[1] Univ Tokyo, Sch Sci, Dept Chem, 7-3-1 Hongo,Bunkyo Ku, Tokyo 1330033, Japan
基金
日本学术振兴会;
关键词
Luciferase; Protein complementation assays; Bioluminescence; Biosensors; SPLIT-LUCIFERASE; BIOLUMINESCENT INDICATOR; LUMINESCENT BIOSENSOR; MAMMALIAN-CELLS; TRACING PROTEIN; SINGLE-CELL; DEEP-TISSUE; EXPRESSION; CDNA; CLONING;
D O I
10.1007/s44211-025-00730-y
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Luciferase complementation assays have emerged in 2001 as a useful tool to analyze biological processes through diverse biological assays such as cellular studies and in vivo imaging. The assay has an advantage of wide dynamic ranges, high signal-to-noise ratios, and capability for real-time monitoring of dynamic biological events with a readout of bioluminescence. While it was initially harnessed for detecting protein-protein interactions, biosensors based on luciferase-fragment complementation have achieved significant advancements in their designs, expanding versatility and applicability beyond the initial scope. This review aims to provide a comprehensive overview of designing strategies employed in split luciferase complementation assays and to highlight their diverse bioanalytical applications. Because simple bi-molecular detection of protein-protein interactions by this approach is well-established, this review will focus on introducing diverse sensor designs using the concept of split luciferase complementation.
引用
收藏
页数:13
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