DNA binding fluorescent proteins as single-molecule probes

被引:12
作者
Jin, Xuelin [1 ,2 ]
Hapsari, Natalia Diyah [1 ,2 ,3 ]
Lee, Seonghyun [1 ,2 ]
Jo, Kyubong [1 ,2 ]
机构
[1] Sogang Univ, Dept Chem, Seoul 04107, South Korea
[2] Sogang Univ, Interdisciplinary Program Integrated Biotechnol, Seoul 04107, South Korea
[3] Sanata Dharma Univ, Chem Educ Program, Dept Math & Sci Educ, Yogyakarta 55282, Indonesia
基金
新加坡国家研究基金会;
关键词
NUCLEAR-LOCALIZATION SIGNAL; NF-KAPPA-B; BACTERIAL CHROMOSOME SEGREGATION; IN-SITU HYBRIDIZATION; GFP FUSION PROTEINS; C-TERMINAL DOMAIN; TRANSCRIPTION FACTOR; ESCHERICHIA-COLI; SUBCELLULAR-LOCALIZATION; CORRELATION SPECTROSCOPY;
D O I
10.1039/d0an00218f
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
DNA binding fluorescent proteins are useful probes for a broad range of biological applications. Fluorescent protein (FP)-tagging allows DNA binding proteins expressed within a living cell to be directly visualised, in real-time, to study DNA binding patterns and dynamics. Moreover, FP-tagged DNA binding proteins (FP-DBP) have allowed the imaging of single proteins bound to large elongated DNA molecules with a fluorescence microscope. Although there are numerous DNA binding proteins, only a small portion of them have been exploited to construct FP-DBPs to study molecular motion in a cell orin vitrosingle-molecule visualisation. Therefore, it would be informative to review FP-DBP for further development. Here, we summarise the design of FP-DBPs and their brightness, photostability, pK(a), maturation rate, and binding affinity (K-d) characteristics. Then, we review the applications of FP-DBP in cells to study chromosome dynamics, DNA replication, transcription factors, DNA damage, and repair. Finally, we focus on single DNA molecule visualisation using FP-DBP.
引用
收藏
页码:4079 / 4095
页数:17
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