Ultrafast Photoinduced Electron Transfer between Tetramethylrhodamine and Guanosine in Aqueous Solution

被引:23
作者
Li, Xun [2 ,3 ]
Zhu, Ruixue [1 ]
Yu, Anchi [1 ]
Zhao, Xin Sheng [2 ,3 ]
机构
[1] Renmin Univ China, Dept Chem, Beijing 100872, Peoples R China
[2] Peking Univ, Beijing Natl Lab Mol Sci, State Key Lab Struct Chem Unstable & Stable Speci, Dept Chem Biol,Coll Chem & Mol Engn, Beijing 100871, Peoples R China
[3] Peking Univ, Biodynam Opt Imaging Ctr, Beijing 100871, Peoples R China
基金
中国国家自然科学基金;
关键词
RESONANCE ENERGY-TRANSFER; SINGLE-MOLECULE FLUORESCENCE; CONFORMATIONAL DYNAMICS; CHARGE-TRANSFER; CORRELATION SPECTROSCOPY; PROTEIN INTERACTIONS; ORGANIC-DYES; DNA-BASE; PROBE; 2-AMINOPURINE;
D O I
10.1021/jp200455b
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Photoinduced electron transfer based fluorescence correlation spectroscopy (PET-FCS) is a powerful tool to study biomolecular processes. However, some questions remain as to how to correctly interpret the PET-FCS data. In this work, we studied the PET process between tetramethylrhodamine and guanosine by means of femtosecond transient absorption spectroscopy. We derived that the charge separation rate is 4.1 x 10(9) s(-1) and the charge recombination rate is 5.2 x 10(10) s(-1) for the current system, supporting the three-state model and the interpretation on PET-FCS experiments given by Qu et al. (J. Phys Chem. B, 2010, 114, 8235). At the limit that both the charge separation and recombination rates are much faster than the process that PET-FCS reveals, the three-state model can be simplified to an equivalent two-state model with a dark state whose brightness is nonzero. We propose ways to obtain the brightness of the dark state with additional experiments, which is necessary for a PET-FCS study.
引用
收藏
页码:6265 / 6271
页数:7
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