Matwijczuk Arkadiusz, Górecki Andrzej, Makowski Marcin, Pustuła Katarzyna, Skrzypek Alicja, Waś Joanna, Niewiadomy Andrzej, Gagoś Mariusz
Department of Biophysics, University of Life Sciences in Lublin, Akademicka 13, 20-950, Lublin, Poland.
Department of Physical Biochemistry, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Gronostajowa 7, 30-387, Krakow, Poland.
J Fluoresc. 2018 Jan;28(1):65-77. doi: 10.1007/s10895-017-2175-2. Epub 2017 Sep 9.
The article presents the results of fluorescence analyses of 2-methylamino-5-(2,4-dihydroxyphenyl)-1,3,4-thiadiazole (MDFT) in an aqueous environment. MDFT dissolved in aqueous solutions with a pH value in the range from 1 to 4.5 yielded an interesting effect of two clearly separated fluorescence emissions. In turn, a single fluorescence was observed in MDFT dissolved in water solutions with a pH value from 4.5 to 12. As it was suggested in the previous investigations of other 1,3,4-thiadiazole compounds, these effects may be associated with conformational changes in the structure of the analysed molecule accompanied by aggregation effects. Crystallographic data showed that the effect of the two separated fluorescence emissions occurred in a conformation with the -OH group in the resorcyl ring bound on the side of the sulphur atom from the 1,3,4-thiadiazole ring. The hypothesis of aggregation as the mechanism involved in the change in the spectral properties at low pH is supported by the results of (Time-Dependent) Density Functional Theory calculations. The possibility of rapid analysis of conformational changes with the fluorescence spectroscopy technique may be rather important outcome obtained from the spectroscopic studies presented in this article. Additionally, the presented results seem to be highly important as they can be easily observed in solutions and biologically important samples.
本文介绍了2-甲氨基-5-(2,4-二羟基苯基)-1,3,4-噻二唑(MDFT)在水性环境中的荧光分析结果。MDFT溶解在pH值范围为1至4.5的水溶液中时,会产生两种明显分离的荧光发射的有趣效果。相反,在pH值为4.5至12的水溶液中溶解的MDFT中观察到单一荧光。正如先前对其他1,3,4-噻二唑化合物的研究所表明的那样,这些效果可能与分析分子结构中的构象变化以及聚集效应有关。晶体学数据表明,两种分离的荧光发射效应发生在间苯二酚环中的-OH基团与1,3,4-噻二唑环中硫原子一侧相连的构象中。(含时)密度泛函理论计算结果支持了聚集是低pH下光谱性质变化所涉及机制的假设。利用荧光光谱技术快速分析构象变化的可能性可能是本文所呈现光谱研究获得的相当重要的成果。此外,所呈现的结果似乎非常重要,因为它们在溶液和具有生物学重要性的样品中很容易观察到。