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作 者:张洁怡[1] 陈艳豪 王凌琴 马婧 Zhang Jieyi;Chen Yanhao;Wang Lingqin;Ma Jing(Chemical Engineering of Northwest Nationalities University,Gansu,73003)
出 处:《当代化工研究》2018年第3期165-167,共3页Modern Chemical Research
基 金:西北民族大学国家级大学生创新创业训练计划资助项目(项目编号201710742084)
摘 要:目的:本文研究了金属离子对白背三七中主要降血糖成分木犀草素、槲皮素、山奈酚分别与牛血清白蛋白(BSA)相互作用的影响。并通过分子模拟进一步探讨了这些药物与牛血清白蛋白、蛋白质结合的作用力。方法主要利用荧光光谱法,在生理条件p H=7.4的条件下,研究了金属离子Mn^(2+)、Co^(2+)、Ni^(2+)对白背三七中木犀草素、槲皮素、山奈酚在常温(298K)下分别与牛血清白蛋白的相互作用对BSA结构的影响。用AUTODOCK中的柔性对接方法从理论上进一步探讨这些药物分别与牛血清白蛋白蛋白质结合的位点和作用力。结果金属离子的存在改变了色氨酸残基的同步荧光峰位置,使之与黄酮-BSA体系相反。得到木犀草素、槲皮素、山奈酚与牛血清白蛋白分子对接结果。结论:金属离子的存在加剧了木犀草素、槲皮素、山奈酚与牛血清白蛋白作用时BSA结构的变化。并通过软件分别求出了三种黄酮成分与BSA相互作用时的结合位点。Objective: This paper studied the effects of metal ions on the interaction of luteolin, quercetin and kaempferol with bovine serum albumin(BSA), and further investigated the binding force between these drugs and bovine serum albumin protein by molecular simulation. Method: Mainly through fluorescence spectroscopy, under physiological conditions of p H=7.4, The effects of metal ions Mn^(2+)、Co^(2+) and Ni^(2+) on the structure of luteolin, quercetin and kaempferol in pseudo-ginseng radix with bovine serum albumin at normal temperature(298 K) were studied. The binding sites and forces of these drugs to bovine serum albumin(BSA) proteins were further investigated theoretically by flexible docking method in AUTODOCK. Result: The presence of metal ions changes the synchronous fluorescence peak position of tryptophan residues, which is opposite to the flavonoid-BSA system. The docking results of luteolin, quercetin, kaempferol and bovine serum albumin molecules were obtained. Conclusion: The presence of metal ions intensifies the structural changes of BSA during the interaction of luteolin, quercetin, kaempferol and bovine serum albumin. The binding sites of interaction of the three flavonoid components with BSA were determined by software.
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