Wataru Shihoya, Aika Iwama, Fumiya K Sano, Osamu Nureki
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引用次数: 0
摘要
G 蛋白偶联受体(GPCRs)是人类的一个重要超家族,分为六类(A 至 F),在细胞通讯和治疗中发挥着不可或缺的作用。然而,由于高分辨率数据采集方面的挑战,对其结构的理解一直受到限制。本综述强调了低温电子显微镜(cryo-EM)在确定 GPCR-G 蛋白复合物结构方面的变革性影响。纳米抗体和迷你 G 蛋白等特定技术可稳定复合物并促进结构测定。我们讨论了不同类别 GPCR 受体激活时的结构变化,揭示了它们的不同机制。这些低温电子显微镜结构为理解 GPCR 的功能奠定了坚实的基础,并为未来药物发现和靶向治疗的突破铺平了道路。
G-protein-coupled receptors (GPCRs) constitute a prominent superfamily in humans and are categorized into six classes (A-F) that play indispensable roles in cellular communication and therapeutics. Nonetheless, their structural comprehension has been limited by challenges in high-resolution data acquisition. This review highlights the transformative impact of cryogenic electron microscopy (cryo-EM) on the structural determinations of GPCR-G-protein complexes. Specific technologies, such as nanobodies and mini-G-proteins, stabilize complexes and facilitate structural determination. We discuss the structural alterations upon receptor activation in different GPCR classes, revealing their diverse mechanisms. This review highlights the robust foundation for comprehending GPCR function and pave the way for future breakthroughs in drug discovery and therapeutic targeting.
期刊介绍:
The Journal of Biochemistry founded in 1922 publishes the results of original research in the fields of Biochemistry, Molecular Biology, Cell, and Biotechnology written in English in the form of Regular Papers or Rapid Communications. A Rapid Communication is not a preliminary note, but it is, though brief, a complete and final publication. The materials described in Rapid Communications should not be included in a later paper. The Journal also publishes short reviews (JB Review) and papers solicited by the Editorial Board.