Swiss Federal Institute of Technology, Laboratory of Physical Chemistry, ETH Zurich, 8093, Zurich, Switzerland.
J Comput Chem. 2014 Dec 15;35(32):2279-87. doi: 10.1002/jcc.23757. Epub 2014 Oct 18.
Olfactory receptors (ORs) represent the largest subfamily of the superfamily G protein-coupled receptors (GPCRs). This family of membrane receptors functions as essential gateway for activation of many cellular signaling pathways. Finding universal principles underlying GPCR activation by studying ORs is important for the design of new therapeutics that target olfaction-related and other GPCR-malfunctioning diseases. In addition, gaining knowledge regarding the interactions between ORs and their cognate ligands (odorants) may contribute to solve the puzzle of how odor perception is encoded in humans. As no crystal structure of an OR is available yet, homology modeling can be applied to generate a three-dimensional OR model. Molecular docking, molecular dynamics simulations and qualitative structure-activity-relationship can further guide experimental research by investigating interactions at the atomic level. This article will review these computational techniques as well as present databases and popular software suites, which can support researchers in the OR research field.
嗅觉受体(ORs)是 G 蛋白偶联受体(GPCRs)超家族中最大的亚家族。这些膜受体作为激活许多细胞信号通路的基本门户。通过研究 ORs 来发现 GPCR 激活的普遍原则对于设计针对嗅觉相关和其他 GPCR 功能障碍疾病的新型治疗方法非常重要。此外,了解 OR 与其同源配体(气味物质)之间的相互作用可能有助于解决人类嗅觉感知是如何编码的难题。由于目前还没有 OR 的晶体结构,因此可以应用同源建模来生成三维 OR 模型。分子对接、分子动力学模拟和定性构效关系可以通过在原子水平上研究相互作用进一步指导实验研究。本文将综述这些计算技术,并介绍支持 OR 研究领域研究人员的数据库和流行软件套件。