Alternating-laser excitation: single-molecule FRET and beyond

被引:128
作者
Hohlbein, Johannes [1 ]
Craggs, Timothy D. [2 ]
Cordes, Thorben [3 ,4 ]
机构
[1] Wageningen UR, Biophys Lab, Wageningen, Netherlands
[2] Univ Oxford, Dept Phys, Oxford, England
[3] Univ Groningen, Mol Microscopy Res Grp, Groningen, Netherlands
[4] Univ Groningen, Zernike Inst Adv Mat, Groningen, Netherlands
基金
欧洲研究理事会;
关键词
RESONANCE ENERGY-TRANSFER; NANO-POSITIONING SYSTEM; DNA-POLYMERASE-I; RNA-POLYMERASE; FLUORESCENCE SPECTROSCOPY; CONFORMATIONAL DYNAMICS; PHOTON DISTRIBUTION; STRUCTURAL HETEROGENEITIES; NUCLEOTIDE SELECTION; TRANSCRIPTION BUBBLE;
D O I
10.1039/c3cs60233h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The alternating-laser excitation (ALEX) scheme continues to expand the possibilities of fluorescence-based assays to study biological entities and interactions. Especially the combination of ALEX and single-molecule Forster Resonance Energy Transfer (smFRET) has been very successful as ALEX enables the sorting of fluorescently labelled species based on the number and type of fluorophores present. ALEX also provides a convenient way of accessing the correction factors necessary for determining accurate molecular distances. Here, we provide a comprehensive overview of the concept and current applications of ALEX and we explicitly discuss how to obtain fully corrected distance information across the entire FRET range. We also present new ideas for applications of ALEX which will push the limits of smFRET-based experiments in terms of temporal and spatial resolution for the study of complex biological systems.
引用
收藏
页码:1156 / 1171
页数:16
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