Dong Jian, Solntsev Kyril M, Tolbert Laren M
School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, Georgia 30332-0400, USA.
J Am Chem Soc. 2006 Sep 20;128(37):12038-9. doi: 10.1021/ja063128a.
The solvatochromic behavior of the green fluorescence protein (GFP) chromophore (p-hydroxybenzylideneimidazolone, p-HBDI) and its derivatives (p-methoxybenzylideneimidazolone, p-MeOBDI, and N-methyl-p-hydroxybenzylideneimidazolonium iodide, p-HBDIMe+) was studied using UV-vis-absorption spectroscopy in a wide array of solvents. The relative contribution of specific (polarity) vs nonspecific (hydrogen-bonding) solvation to the absorbance spectra was studied. On the basis of these data, we discuss the nature of the absorption peak of the protonated and deprotonated forms of the wild-type GFP.
利用紫外可见吸收光谱法,在多种溶剂中研究了绿色荧光蛋白(GFP)发色团(对羟基苄叉咪唑啉酮,p-HBDI)及其衍生物(对甲氧基苄叉咪唑啉酮,p-MeOBDI,以及N-甲基-对羟基苄叉咪唑鎓碘化物,p-HBDIMe+)的溶剂化显色行为。研究了特异性(极性)与非特异性(氢键)溶剂化对吸收光谱的相对贡献。基于这些数据,我们讨论了野生型GFP质子化和去质子化形式吸收峰的性质。