Advances in Quantitative FRET-Based Methods for Studying Nucleic Acids

被引:108
作者
Preus, Soren [2 ]
Wilhelmsson, L. Marcus [1 ]
机构
[1] Chalmers Univ Technol, Dept Chem & Biol Engn, S-41296 Gothenburg, Sweden
[2] Univ Copenhagen, Dept Chem, DK-2100 Copenhagen, Denmark
基金
瑞典研究理事会;
关键词
DNA structures; fluorescence spectroscopy; fluorescent probes; FRET; nucleic acids; RESONANCE ENERGY-TRANSFER; SINGLE-MOLECULE FRET; ALTERNATING-LASER EXCITATION; DOUBLE-STRANDED DNA; NANO-POSITIONING SYSTEM; PHOTOINDUCED ELECTRON-TRANSFER; FLUORESCENCE PROPERTIES; CONFORMATIONAL DYNAMICS; PHOTON DISTRIBUTION; STRUCTURAL HETEROGENEITIES;
D O I
10.1002/cbic.201200400
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Forster resonance energy transfer (FRET) is a powerful tool for monitoring molecular distances and interactions at the nanoscale level. The strong dependence of transfer efficiency on probe separation makes FRET perfectly suited for on/off experiments. To use FRET to obtain quantitative distances and three-dimensional structures, however, is more challenging. This review summarises recent studies and technological advances that have improved FRET as a quantitative molecular ruler in nucleic acid systems, both at the ensemble and at the single-molecule levels.
引用
收藏
页码:1990 / 2001
页数:12
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