Fluorescence anisotropy decay for intramolecular two-state excited-state processes with added quencher in the presence of rotational diffusion: An identifiability analysis

被引:4
|
作者
Szubiakowski, Jacek P.
Dale, Robert E.
Boens, Noel
Ameloot, Marcel
机构
[1] Hasselt Univ, Biomed Res Inst, B-3590 Diepenbeek, Belgium
[2] Transnatl Univ Limburg, B-3590 Diepenbeek, Belgium
[3] Katholieke Univ Leuven, Dept Chem, B-3001 Heverlee, Belgium
[4] Kings Coll London, Sch Biomed & Hlth Sci, Randall Div Cell & Mol Biophys, London SE1 1UL, England
[5] Univ Warmia & Masuria Olszytn, Dept Phys & Comp Methods, PL-10561 Olsztyn, Poland
关键词
D O I
10.1016/j.cplett.2007.02.051
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
A deterministic identifiability analysis of kinetic models of a reversible intramolecular excited-state process involving species-dependent rotational Brownian diffusion is performed for spherical and cylindrically symmetric rotors. It is assumed that the axes of rotation do not change upon interconversion, and that the rate constants are independent of orientation. Use of three quencher concentrations allows the determination of two internally consistent sets of quenching rate constants, combinations of excited-state deactivation/exchange rate constants, individual rotational diffusion coefficients, relative orientations of transition moments, and restricted spectral information. Assignment of each set obtained to a particular species is not possible without additional prior information. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:113 / 118
页数:6
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