摘要
谷氨酰胺结合蛋白(Glutamine-bindingprotein,GlnBp)是大肠杆菌透性酶系统中一个细胞外液底物专一性结合蛋白,对于细胞外液中谷氨酰胺(Gln)的运输和传递至关重要.本文运用分子动力学(Moleculardynamics,MD)模拟采样,考察了GlnBp关键残基与底物Gln之间的相互作用和GlnBp两条铰链的功能差别;并采用MM-PBSA方法计算了GlnBp与底物Gln的结合自由能.结果表明:Ph13,Phe50,Thr118和Ile69与底物Gln的范德华相互作用和Arg75,Thr70,Asp157,Gly68,Lys115,Ala67,His156与底物Gln的静电相互作用是结合Gln的主要推动力;复合物的铰链区85～89柔性大,对构象开合提供了结构基础;而铰链区181～185柔性小,其作用更多是在功能上把底物Gln限制在口袋中;自由能预测值与实验值吻合.本研究很好地解释了GlnBp结构与功能的关系,为进一步了解GlnBp的开合及转运Gln的机制提供了重要的结构信息.
Glutamine-binding protein （GlnBp） is one of the ligand-specific periplasmic binding proteins in the Escherichia coli permease systems, predicted to play an important role in transferring Gln from the periplasmic space to the cytoplasmic space. In this paper, the interaction of the key residues in GlnBp with the ligand Gln and the functional difference between the two hinges in GlnBp were evaluated through molecular dynamics simulation sampling, and the binding free energy of GlnBp with Gln was calculated by the MM-PBSA method. The results show that the main impetus to bind Gin lies in the van der Waals＇（VDW） interactions between Gin and Phe13, Phe50, Thr118, Ile69, as well as the electrostatic interactions between Arg75, Thr70, Asp157, Gly68, Lys115, Ala67, His156 and ligand Gin. The hinge region 85-89 whose fluctuation is larger than the hinge region 181 - 185 has a more flexibility which can provide a structural basis to bind ligand Gin, while the main function of the hinge region 181-185 was proposed to restrict ligand Gin in the pocket of GlnBp. It is found that the result predicted with the MM-PBSA method agrees well with experimental data. The relationship between the structure and function of GlnBp is well illustrated, which provides us with some important structural information on the open-close mechanism of GlnBp and the transportation of Gin.
出处
《化学学报》
SCIE
CAS
CSCD
北大核心
2006年第20期2079-2085,共7页
Acta Chimica Sinica
基金
国家自然科学基金(Nos.10574009
30400087)
教育部博士点基金(No.20040005013)
北京市自然科学基金(No.5042003)资助项目.
