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Preferential Coupling of Dopamine D2S and D2L Receptor Isoforms with Gi1 and Gi2 Proteins—In Silico Study

机译:多巴胺D2s和D2L受体同种型与Gi1和Gi2蛋白 - 在硅研究中的优先偶联

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摘要

The dopamine D2 receptor belongs to rhodopsin-like G protein-coupled receptors (GPCRs) and it is an important molecular target for the treatment of many disorders, including schizophrenia and Parkinson’s disease. Here, computational methods were used to construct the full models of the dopamine D2 receptor short (D2S) and long (D2L) isoforms (differing with 29 amino acids insertion in the third intracellular loop, ICL3) and to study their coupling with Gi1 and Gi2 proteins. It was found that the D2L isoform preferentially couples with the Gi2 protein and D2S isoform with the Gi1 protein, which is in accordance with experimental data. Our findings give mechanistic insight into the interplay between isoforms of dopamine D2 receptors and Gi proteins subtypes, which is important to understand signaling by these receptors and their mediation by pharmaceuticals, in particular psychotic and antipsychotic agents.
机译:多巴胺D2受体属于罗霉蛋白样G蛋白偶联受体(GPCR),它是治疗许多疾病的重要分子靶标,包括精神分裂症和帕金森病。这里,计算方法用于构建多巴胺D2受体短(D2S)和长(D2L)同种型的完整模型(与第三细胞内环,ICL3中的29个氨基酸插入不同,并研究其与GI1和Gi2的偶联蛋白质。发现D2L同种型优先与GI2蛋白和D2S同种型与GI1蛋白相互作用,这是根据实验数据的。我们的调查结果对多巴胺D2受体和GI蛋白亚型的同种型之间的相互作用,这对于通过这些受体和药物的调解,特别是精神病和抗精神病药物的调解非常重要。

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