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Lessons from Free Energy Simulations of δ-Opioid Receptor Homodimers Involving the Fourth Transmembrane Helix

机译:涉及第四跨膜螺旋的δ阿片受体均聚物自由能模拟的经验教训

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摘要

Several G protein-coupled receptors (GPCRs), including opioid receptors δOR, μOR, and κOR, have been reported to form stable dimers or oligomers in lipid bilayers and cell membranes. This notion has been recently challenged by imaging data supporting a transient nature of GPCR association. Here we use umbrella sampling reconstructed free energies of δOR homodimers involving the fourth transmembrane helix to predict their association constant. The results of these simulations, combined with estimates of diffusion-limited association rates, suggest a short lifetime for δOR homodimers in the membrane, in agreement with recent trends.
机译:据报道,几种G蛋白偶联受体(GPCR),包括阿片受体δOR,μOR和κOR,在脂质双层和细胞膜中形成稳定的二聚体或寡聚体。最近,通过支持GPCR关联的瞬时性质的成像数据对这一概念提出了挑战。在这里,我们使用涉及第四跨膜螺旋的δOR同二聚体的伞状采样重构自由能来预测其缔合常数。这些模拟的结果与扩散受限缔合速率的估计相结合,表明膜中δOR同二聚体的寿命较短,与最近的趋势一致。

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