Silvi Antonini P, Hillen W, Ettner N, Hinrichs W, Fantucci P, Doglia S M, Bousquet J A, Chabbert M
Dipartimento di Chimica Inorganica and Metallorganica, Univerità degli Studi di Milano, Italy.
Biophys J. 1997 Apr;72(4):1800-11. doi: 10.1016/S0006-3495(97)78826-X.
A 35% decrease in the fluorescence intensity of F75 TetR Trp-43 was observed upon binding of the tetracycline derivative 5a,6-anhydrotetracycline (AnTc) to the repressor. The fluorescence decay of Trp-43 in F75 TetR and in its complex with AnTc could be described by the sum of three exponential components, with lifetimes of about 6, 3, and 0.3 ns. The amplitudes, however, were markedly altered upon binding. The minimized energy mapping of Trp-43 chi 1 x chi 2 isomerization clearly indicated the existence of three main potential wells at positions (-160 degrees, -90 degrees) (rotamer I), (-170 degrees, 90 degrees) (rotamer II), and (-70, 150 degrees) (rotamer III). Our study of Trp-43 environment for each of the three rotamers suggests that the longest decay component may be assigned to rotamer II, the middle-lived component to rotamer I, and the subnanosecond component to rotamer III. The origin of the changes in the rotamer distribution upon AnTc binding is discussed. Anisotropy decays are also discussed within the framework of the rotamer model.
当四环素衍生物5a,6-脱水四环素(AnTc)与阻遏物结合时,观察到F75 TetR Trp-43的荧光强度下降了35%。F75 TetR及其与AnTc复合物中Trp-43的荧光衰减可用三个指数成分的总和来描述,寿命分别约为6、3和0.3纳秒。然而,结合后振幅发生了显著变化。Trp-43 χ1 χ2异构化的最小能量图谱清楚地表明,在(-160度,-90度)(旋转异构体I)、(-170度,90度)(旋转异构体II)和(-70度,150度)(旋转异构体III)位置存在三个主要的势阱。我们对三种旋转异构体中Trp-43环境的研究表明,最长的衰减成分可能归属于旋转异构体II,中等寿命的成分归属于旋转异构体I,亚纳秒成分归属于旋转异构体III。讨论了AnTc结合后旋转异构体分布变化的起源。还在旋转异构体模型的框架内讨论了各向异性衰减。