The solvatochromic effects of side chain substitution on the binding interaction of novel tricarbocyanine dyes with human serum albumin
- 作者：Garfield Beckford ; Eric Owens ; Maged Henary ; Gabor Patonay ; gpatonay@gsu.edu
- 关键词：Human Serum Albumin (HSA) ; Steric specificity ; Solvatochromism ; Near-infrared laser induced fluorescence (NIR-LIF) spectroscopy ; J-aggregation (Bathochromic) and H-aggregation (Hypsochromic)
- 刊名：Talanta
- 出版年：2012
- 期刊代码：106_00399140
- 类别：ch
- 出版时间：15 April, 2012
- 卷：92
- 期：Complete
- 页码：45-52
- 文件大小：1769 K
摘要
The effects of solvatochromism on protein-ligand interactions have been studied by absorbance and near-infrared laser induced fluorescence (NIR-LIF) spectroscopy. The utility of three novel classes of cyanine dyes designed for this purpose illustrates that the affinity interactions of ligands at the hydrophobic binding pockets of Human Serum Albumin (HSA) are not only dependent on the overall hydrophobic characteristics of the molecules but are highly influenced by the size of the ligands as well. Whereas changes to the chromophore moiety exhibited slight to moderate changes to the hydrophobic nature of these molecules, substitution at the alkyl indolium side chain has enabled us to vary the binding affinity towards serum albumin. Substitution at the indolium side chain among an ethyl to butyl group results in improved binding characteristics and an almost three-fold increase in affinity constant. In addition, replacement of the ethyl side chain with a phenylpropyl group also yielded unique solvotachromic patterns such as increased hydrophobicity and subsequent biocompatibility with the HSA binding regions. Ligand interaction was however inhibited by steric hindrance associated with the bulky phenyl ring system thus affecting the increased binding that could be realized from the improved hydrophobic nature of the molecules. This characteristic change in binding affinity is of potential interest to developing a methodology which reveals information on the hydrophobic character and steric specificity of the binding cavities.