Three-dimensional orientational colocalization of individual donor-acceptor pairs

被引:25
作者
Hübner, CG
Ksenofontov, V
Nolde, F
Müllen, K
Basché, T
机构
[1] Univ Mainz, D-55099 Mainz, Germany
[2] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
关键词
D O I
10.1063/1.1760492
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
We report on the determination of the three-dimensional orientation of the donor and acceptor transition dipoles in individual fluorescence resonance energy transfer (FRET) pairs by means of scanning optical microscopy with annular illumination. Knowledge of the mutual orientation of the donor and acceptor dipole is mandatory for reliable distance determination based on FRET efficiency measurements. In our model system perylenediimide as the donor and terryelenediimide as the acceptor are coupled via a stiff p-terphenyl linker. The absorption dipoles of the donor and acceptor are selectively addressed by the 488 nm and 647 line of an Ar/Kr mixed gas laser, respectively. A clear deviation from collinearity is observed with a distribution of misalignment angles peaked around 22degrees. (C) 2004 American Institute of Physics.
引用
收藏
页码:10867 / 10870
页数:4
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