Pogozheva Irina D, Przydzial Magdalena J, Mosberg Henry I
Department of Medicinal Chemistry, College of Pharmacy, University of Michigan, Ann Arbor, MI 48109, USA.
AAPS J. 2005 Oct 5;7(2):E434-48. doi: 10.1208/aapsj070243.
Opioid receptors interact with a variety of ligands, including endogenous peptides, opiates, and thousands of synthetic compounds with different structural scaffolds. In the absence of experimental structures of opioid receptors, theoretical modeling remains an important tool for structure-function analysis. The combination of experimental studies and modeling approaches allows development of realistic models of ligand-receptor complexes helpful for elucidation of the molecular determinants of ligand affinity and selectivity and for understanding mechanisms of functional agonism or antagonism. In this review we provide a brief critical assessment of the status of such theoretical modeling and describe some common problems and their possible solutions. Currently, there are no reliable theoretical methods to generate the models in a completely automatic fashion. Models of higher accuracy can be produced if homology modeling, based on the rhodopsin X-ray template, is supplemented by experimental structural constraints appropriate for the active or inactive receptor conformations, together with receptor-specific and ligand-specific interactions. The experimental constraints can be derived from mutagenesis and cross-linking studies, correlative replacements of ligand and receptor groups, and incorporation of metal binding sites between residues of receptors or receptors and ligands. This review focuses on the analysis of similarity and differences of the refined homology models of mu, delta, and kappa-opioid receptors in active and inactive states, emphasizing the molecular details of interaction of the receptors with some representative peptide and nonpeptide ligands, underlying the multiple modes of binding of small opiates, and the differences in binding modes of agonists and antagonists, and of peptides and alkaloids.
阿片受体可与多种配体相互作用,包括内源性肽、阿片类药物以及数千种具有不同结构支架的合成化合物。在缺乏阿片受体实验结构的情况下,理论建模仍然是结构功能分析的重要工具。实验研究与建模方法相结合,有助于开发逼真的配体-受体复合物模型,这有助于阐明配体亲和力和选择性的分子决定因素,并有助于理解功能激动或拮抗的机制。在本综述中,我们对这种理论建模的现状进行了简要的批判性评估,并描述了一些常见问题及其可能的解决方案。目前,尚无可靠的理论方法以完全自动化的方式生成模型。如果基于视紫红质X射线模板的同源建模辅以适合活性或非活性受体构象的实验结构约束,以及受体特异性和配体特异性相互作用,则可以生成更高精度的模型。实验约束可源自诱变和交联研究、配体和受体基团的相关替换,以及在受体残基之间或受体与配体之间引入金属结合位点。本综述着重分析μ、δ和κ阿片受体在活性和非活性状态下的精细同源模型的异同,强调受体与一些代表性肽和非肽配体相互作用的分子细节,这些细节构成了小阿片类药物多种结合模式的基础,以及激动剂和拮抗剂、肽和生物碱结合模式的差异。