化学
黄烷酮
氢键
类黄酮
猝灭(荧光)
数量结构-活动关系
位阻效应
疏水效应
立体化学
范德瓦尔斯力
结合位点
荧光光谱法
荧光
计算化学
有机化学
生物化学
抗氧化剂
分子
物理
量子力学
作者
Chengyun He,Lu Bai,Daqun Liu,Benguo Liu
标识
DOI:10.1016/j.fochx.2023.101023
摘要
The binding capacity of 10 flavonoids with okra seed protein (OSP) was studied by fluorescence spectroscopy. The structure of flavonoids had an obvious impact on binding performance. The binding ability of flavanone was lower than that of flavone, isoflavone and dihydrochalcone. The binding capacity of flavonoid glycoside was superior to that of the corresponding flavonoid aglycone. The binding ability was positively correlated with the number of phenolic hydroxyl groups on the B ring. The steric field and electrostatic field model constructed by 3D-QSAR method could well explain the above interaction behavior. Thermodynamic analysis suggested that the quenching mechanism of OSP caused by flavonoids was static quenching, and the binding-site number was 1. In addition, hydrogen bonding and van der Waals force dominated this interaction. The 3D and synchronous fluorescence spectra showed that there was no significant change in the polarity of the environment around tryptophan and tyrosine residues during binding.
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