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Model of the whole rat AT1 receptor and the ligand-binding site

机译:整个大鼠AT1 受体的模型及其配体结合位点

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摘要

We present a three-dimensional model of the rat type 1 receptor (AT1) for the hormone angiotensin II (Ang II). Ang II and the AT1 receptor play a critical role in the cell-signaling process responsible for the actions of renin–angiotensin system in the regulation of blood pressure, water-electrolyte homeostasis and cell growth. Development of improved therapeutics would be significantly enhanced with the availability of a 3D-structure model for the AT1 receptor and of the binding site for agonists and antagonists. This model was constructed using a combination of computation and homology-modeling techniques starting with the experimentally determined three-dimensional structure of bovine rhodopsin (PDB#1F88) as a template. All 359 residues and two disulfide bonds in the rat AT1 receptor have been accounted for in this model. Ramachandran-map analysis and a 1 nanosecond molecular dynamics simulation of the solvated receptor with and without the bound ligand, Ang II, lend credence to the validity of the model. Docking calculations were performed with the agonist, Ang II and the antihypertensive antagonist, losartan.
机译:我们提出了大鼠血管紧张素II(Ang II)1型受体(AT1 )的三维模型。 Ang II和AT1 受体在负责肾素-血管紧张素系统调节血压,水电解质稳态和细胞生长的细胞信号传导过程中起关键作用。有了AT1 受体的3D结构模型以及激动剂和拮抗剂的结合位点,就可以大大改善改进治疗方法的开发。使用计算和同源性建模技术的组合,以实验确定的牛视紫红质的三维结构(PDB#1F88)为模板,构建了该模型。该模型解释了大鼠AT1 受体中所有359个残基和两个二硫键。 Ramachandran-map分析和有或没有结合配体Ang II的溶剂化受体的1纳秒分子动力学模拟都证明了该模型的有效性。用激动剂Ang II和降压拮抗剂洛沙坦进行对接计算。

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