Baleanu-Gogonea Camelia, Karnik Sadashiva
Department of Molecular Cardiology at Lerner Research Institute, The Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, OH 44195, USA.
J Mol Model. 2006 Feb;12(3):325-37. doi: 10.1007/s00894-005-0049-z. Epub 2006 Jan 11.
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. [Figure: see text].
我们展示了大鼠1型血管紧张素II(Ang II)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、水电解质平衡及细胞生长作用的细胞信号传导过程中发挥关键作用。若能获得AT1受体的三维结构模型以及激动剂和拮抗剂的结合位点,将显著促进改进型治疗药物的研发。该模型是通过计算和同源建模技术相结合构建而成的,以实验测定的牛视紫红质三维结构(PDB#1F88)作为模板。此模型涵盖了大鼠AT1受体的所有359个残基和两个二硫键。对结合和未结合配体Ang II的溶剂化受体进行的拉马钱德兰图分析和1纳秒分子动力学模拟,证实了该模型的有效性。使用激动剂Ang II和抗高血压拮抗剂氯沙坦进行了对接计算。[图:见正文]