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Analysis of G-protein-coupled receptor dimerization following chemokine signaling.

机译:趋化因子信号转导后G蛋白偶联受体二聚化的分析。

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摘要

An abundance of information has been generated in recent decades on the signaling events triggered through G-protein-coupled receptors (GPCRs). Nonetheless, the structural changes at the cell surface that provoke receptor activation are only now beginning to be understood. It is becoming clear that receptors are not isolated entities that are activated following ligand binding, but that they interact with other molecules already present or recruited to the vicinity, which results in a wide variety of new signaling possibilities. Understanding receptor interactions with relatives and/or friends on the cell surface is thus critical. The most important point is to determine which of these interactions are "casual" and which give rise to functional consequences.
机译:近几十年来,关于由G蛋白偶联受体(GPCR)触发的信号转导事件已经产生了大量信息。尽管如此,引起受体激活的细胞表面结构变化才刚刚开始被理解。越来越清楚的是,受体不是在配体结合后被激活的分离的实体,而是它们与已经存在或募集到附近的其他分子相互作用,这导致了各种各样的新信号传导可能性。因此,了解受体与细胞表面上的亲戚和/或朋友的相互作用至关重要。最重要的一点是确定其中哪些交互是“偶然的”,哪些会引起功能性后果。

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