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8-苯胺基-1-萘磺酸盐分子的自缔合:光谱表征及其在蛋白质折叠研究中的应用

Self-association of 8-anilino-1-naphthalene-sulfonate molecules: spectroscopic characterization and application to the investigation of protein folding.

作者信息

Uversky V N, Winter S, Löber G

机构信息

Institute of Protein Research, Russian Academy of Sciences, 142292 Pushchino, Moscow Region, Russia.

出版信息

Biochim Biophys Acta. 1998 Oct 14;1388(1):133-42. doi: 10.1016/s0167-4838(98)00173-3.

Abstract

It was suggested long ago that the reason for the considerable increase of 8-anilino-1-naphthalene-sulfonate (8-ANS) fluorescence intensity upon the transition from aqueous to organic solvents is the dissociation of 8-ANS associates. To clarify this point the dependence of spectral properties of the dye on concentration and solvent composition was investigated by means of steady-state and time-resolved fluorescence spectroscopy. It was shown that the increase of 8-ANS concentration leads to the changes in the shape of absorption and fluorescence spectra of the dye, accompanied by the decrease in its fluorescence decay time values. Such changes were observed in aqueous and organic solvents for Mg2+- and NH+4-salts of 8-anilino-1-naphthalene-sulfonateic acid and reflect the existence of self-association of the dye molecules in both media. However, the decrease in fluorescence intensity induced by the self-association of the probe molecules is too small to explain weak fluorescence of 8-ANS in water. At the same time, it expounds the difference between the decay times of protein-embedded 8-ANS molecules upon interaction of this probe with native and molten globule proteins.

摘要

很久以前就有人提出,8-苯胺基-1-萘磺酸盐(8-ANS)从水溶液转变为有机溶剂时荧光强度显著增加的原因是8-ANS缔合体的解离。为了阐明这一点,通过稳态和时间分辨荧光光谱研究了染料的光谱性质对浓度和溶剂组成的依赖性。结果表明,8-ANS浓度的增加导致染料吸收光谱和荧光光谱形状的变化,同时伴随着其荧光衰减时间值的降低。在8-苯胺基-1-萘磺酸的Mg2+和NH4+盐的水溶液和有机溶剂中都观察到了这种变化,这反映了染料分子在两种介质中都存在自缔合现象。然而,探针分子自缔合引起的荧光强度降低太小,无法解释8-ANS在水中的弱荧光。同时,这也解释了该探针与天然蛋白质和熔球态蛋白质相互作用时,嵌入蛋白质中的8-ANS分子衰减时间的差异。

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