Theoretical Studies of Short Polyproline Systems: Recalibration of a Molecular Ruler

被引:33
作者
Dolghih, Elena [1 ,2 ]
Ortiz, Wilfredo [1 ,2 ]
Kim, Seonah [1 ,2 ]
Krueger, Brent P. [3 ]
Krause, Jeffrey L. [1 ,2 ]
Roitberg, Adrian E. [1 ,2 ]
机构
[1] Univ Florida, Quantum Theory Project, Gainesville, FL 32611 USA
[2] Univ Florida, Dept Chem, Gainesville, FL 32611 USA
[3] Hope Coll, Dept Chem, Holland, MI 49422 USA
关键词
RESONANCE ENERGY-TRANSFER; SPECTROSCOPIC RULER; EXCITATION TRANSFER; FLUORESCENCE SPECTROSCOPY; RHODOPSEUDOMONAS-ACIDOPHILA; FORSTER THEORY; DYNAMICS; DEPENDENCE; DISTANCE; FRET;
D O I
10.1021/jp811395r
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
FRET experiments enable studies of the chemical and physical properties of individual molecules, which has long been a dream of chemists. However, these modem experimental techniques are still limited by the lack of information about the dynamic behavior of the fluorescent labels as well as by the use of dipole-dipole approximation even at short donor-to-acceptor distances. Our results help to suggest that these assumptions need to be carefully considered when designing experiments. We show that at short donor-acceptor separation, dipole-dipole approximation breaks down and Forster theory fails and cannot be used to obtain correct distances. We also explicitly demonstrate that dyes' linkers allow for a lot of flexibility in the fluorescent label orientation and position resulting in distances much shorter than assumed earlier.
引用
收藏
页码:4639 / 4646
页数:8
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