Department of Pharmacology and Systems Therapeutics, Mount Sinai School of Medicine, One Gustave L. Levy Place, New York, NY10029, USA.
Trends Pharmacol Sci. 2010 Mar;31(3):124-30. doi: 10.1016/j.tips.2009.11.008. Epub 2010 Jan 7.
G-protein-coupled receptors (GPCRs) are membrane proteins that convert extracellular information into intracellular signals. They are involved in many biological processes and therefore represent powerful targets to modulate physiological and pathological states. Recent studies have demonstrated that GPCR activity is regulated by several mechanisms. Among these, protein-protein interactions (and in particular interactions with other receptors leading to heteromerization) has been shown to have an important role in modulating GPCR function. This has expanded their repertoire of signaling and added a new level of regulation to their physiological roles. Emerging studies provide evidence for tissue-specific and disease-specific receptor heteromerization. This suggests that heteromers represent novel drug targets for the identification of selective compounds with potentially fewer side-effects.
G 蛋白偶联受体(GPCRs)是一种将细胞外信息转化为细胞内信号的膜蛋白。它们参与许多生物过程,因此是调节生理和病理状态的有力靶点。最近的研究表明,GPCR 活性受到多种机制的调节。在这些机制中,蛋白质-蛋白质相互作用(特别是与其他受体的相互作用导致异源二聚化)已被证明在调节 GPCR 功能方面发挥着重要作用。这扩展了它们的信号转导谱,并为其生理作用增加了新的调节层次。新兴的研究为组织特异性和疾病特异性受体异源二聚体提供了证据。这表明,异源二聚体代表了新型药物靶点,用于鉴定潜在副作用更少的选择性化合物。