Department of Chemistry and Molecular Biology, University of Gothenburg, Göteborg, Sweden.
J Comput Aided Mol Des. 2013 Mar;27(3):277-91. doi: 10.1007/s10822-013-9640-z. Epub 2013 Apr 4.
Prediction of 3D structures of membrane proteins, and of G-protein coupled receptors (GPCRs) in particular, is motivated by their importance in biological systems and the difficulties associated with experimental structure determination. In the present study, a novel method for the prediction of 3D structures of the membrane-embedded region of helical membrane proteins is presented. A large pool of candidate models are produced by repacking of the helices of a homology model using Monte Carlo sampling in torsion space, followed by ranking based on their geometric and ligand-binding properties. The trajectory is directed by weak initial restraints to orient helices towards the original model to improve computation efficiency, and by a ligand to guide the receptor towards a chosen conformational state. The method was validated by construction of the β1 adrenergic receptor model in complex with (S)-cyanopindolol using bovine rhodopsin as template. In addition, models of the dopamine D2 receptor were produced with the selective and rigid agonist (R)-N-propylapomorphine ((R)-NPA) present. A second quality assessment was implemented by evaluating the results from docking of a library of 29 ligands with known activity, which further discriminated between receptor models. Agonist binding and recognition by the dopamine D2 receptor is interpreted using the 3D structure model resulting from the approach. This method has a potential for modeling of all types of helical transmembrane proteins for which a structural template with sequence homology sufficient for homology modeling is not available or is in an incorrect conformational state, but for which sufficient empirical information is accessible.
预测膜蛋白的 3D 结构,尤其是 G 蛋白偶联受体(GPCR)的 3D 结构,是因为它们在生物系统中的重要性以及实验确定结构所带来的困难。在本研究中,提出了一种预测螺旋膜蛋白膜嵌入区域 3D 结构的新方法。通过在扭转空间中使用蒙特卡罗采样对同源模型的螺旋进行重新组装,产生了大量候选模型,然后根据其几何形状和配体结合特性对它们进行排序。该轨迹通过弱初始约束来引导,使螺旋朝向原始模型定向,以提高计算效率,并通过配体引导受体朝向所选构象状态。该方法通过使用牛视紫红质作为模板构建β1 肾上腺素能受体与(S)-氰基吲哚洛尔复合物进行了验证。此外,还生成了多巴胺 D2 受体与选择性刚性激动剂(R)-N-丙基阿朴吗啡((R)-NPA)存在时的模型。通过评估具有已知活性的 29 种配体库的对接结果,实施了第二个质量评估,这进一步区分了受体模型。使用该方法得出的 3D 结构模型来解释多巴胺 D2 受体的激动剂结合和识别。该方法适用于建模所有类型的螺旋跨膜蛋白,对于没有足够同源性的结构模板的蛋白或处于不正确构象状态的蛋白,只要有足够的经验信息可用,该方法都可以使用。