Single-Molecule Monitoring of the Structural Switching Dynamics of Nucleic Acids through Controlling Fluorescence Blinking

被引:9
作者
Kawai, Kiyohiko [1 ]
Miyata, Takafumi [2 ]
Shimada, Naohiko [2 ]
Ito, Syoji [3 ,4 ]
Miyasaka, Hiroshi [3 ,4 ]
Maruyama, Atsushi [2 ]
机构
[1] Osaka Univ, Inst Sci & Ind Res SANKEN, Mihogaoka 8-1, Ibaraki, Osaka 5670047, Japan
[2] Tokyo Inst Technol, Dept Life Sci & Technol, Midori Ku, 4259 B-57 Nagatsuta, Yokohama, Kanagawa 2268501, Japan
[3] Osaka Univ, Div Frontier Mat Sci, Grad Sch Engn Sci, Toyonaka, Osaka 5678531, Japan
[4] Osaka Univ, Ctr Promot Adv Interdisciplinary Res, Grad Sch Engn Sci, Toyonaka, Osaka 5678531, Japan
关键词
fluorescence; nucleic acids; RNA structures; sensors; single-molecule studies; RESONANCE ENERGY-TRANSFER; CORRELATION SPECTROSCOPY; CONFORMATIONAL DYNAMICS; CHARGE-TRANSFER; DNA; KINETICS; CELL; FLUOROPHORE; PROBES; GUIDE;
D O I
10.1002/anie.201708705
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Single-molecule fluorescence resonance energy transfer (smFRET) is a powerful tool to investigate the dynamics of biomolecular events in real time. However, it requires two fluorophores and can be applied only to dynamics that accompany large changes in distance between the molecules. Herein, we introduce a method for kinetic analysis based on control of fluorescence blinking (KACB), a general approach to investigate the dynamics of biomolecules by using a single fluorophore. By controlling the kinetics of the redox reaction the blinking kinetics or pattern can be controlled to be affected by microenvironmental changes around a fluorophore (rKACB), thereby enabling real-time single-molecule measurement of the structure-changing dynamics of nucleic acids.
引用
收藏
页码:15329 / 15333
页数:5
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