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Investigation of the Binding Between Pepsin and Nucleoside Analogs by Spectroscopy and Molecular Simulation

Journal 2015 · IF 1.927 · 25(2): 451-463 · 发表于 2015 年 2 月 27 日
作者: Li Zhen,Li Zhigang,Yang Lingling,Xie Yuanzhe,Shi Jie,Wang Ruiyong,Chang Junbiao
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摘要

In this paper, the interactions of pepsin with CYD (cytidine) or nucleoside analogs, including FNC (2′-deoxy-2′-β-fluoro-4′-azidocytidine) and CMP (cytidine monophosphate), were investigated by fluorescence, UV–visible absorption and synchronous fluorescence spectroscopy under mimic physiological conditions. The results indicated that FNC (CYD/CMP) caused the fluorescence quenching by the formation of complex. The binding constants and thermo-dynamic parameters at three different temperatures were obtained. The hydrophobic and electrostatic interactions were the predominant intermolecular forces to stabilize the complex. The F atom in FNC might weaken the binding of nucleoside analog to pepsin. Results showed that CYD was the strongest quencher and bound to pepsin with higher affinity.