Boens Noël, Novikov Eugene, Ameloot Marcel
Department of Chemistry, Katholieke Universiteit Leuven, Celestijnenlaan 200 F, 3001 Heverlee, Belgium.
Chemphyschem. 2006 Dec 11;7(12):2559-66. doi: 10.1002/cphc.200600309.
We present the results of the deterministic identifiability analysis based on similarity transformation for models of one-state excited-state events of cylindrically symmetric rotors in isotropic environments undergoing rotational diffusion described by Brownian reorientation. Such an analysis on error-free time-resolved fluorescence (anisotropy) data can reveal whether the parameters of the considered model can be determined. The fluorescence delta-response functions I(parallel)(t) and I(perpendicular)(t), for fluorescence polarized respectively parallel and perpendicular to the electric vector of linearly polarized excitation, are used to construct, in convenient matrix form, expressions of the sum S(t) = I(parallel)(t) + 2I(perpendicular)(t), the difference D(t) = I(parallel)(t) - I(perpendicular)(t), and the time-resolved fluorescence anisotropy r(t) = D(t)/S(t). The identifiability analysis of r(t) demonstrates that the rotational diffusion coefficients D(parallel) and D(perpendicular) for rotation respectively about and perpendicular to the symmetry axis can be uniquely resolved. However, the polar and azimuthal angles defining the absorption and emission transition moments in the molecular reference frame are not individually identifiable. Nevertheless, the difference between the polar angles of these transition moments is uniquely determined.
我们给出了基于相似变换的确定性可识别性分析结果,该分析针对的是在经历布朗重取向描述的旋转扩散的各向同性环境中圆柱对称转子的单态激发态事件模型。对无误差的时间分辨荧光(各向异性)数据进行这样的分析,可以揭示所考虑模型的参数是否能够确定。分别平行和垂直于线偏振激发电矢量偏振的荧光的δ响应函数(I_{||}(t))和(I_{\perp}(t)),用于以方便的矩阵形式构建总和(S(t)=I_{||}(t)+2I_{\perp}(t))、差值(D(t)=I_{||}(t)-I_{\perp}(t))以及时间分辨荧光各向异性(r(t)=D(t)/S(t))的表达式。对(r(t))的可识别性分析表明,分别绕对称轴和平行于对称轴旋转的旋转扩散系数(D_{||})和(D_{\perp})可以唯一确定。然而,在分子参考系中定义吸收和发射跃迁矩的极角和方位角不能单独识别。尽管如此,这些跃迁矩的极角之差是唯一确定的。