iHuman Institute, School of Life Science and Technology, ShanghaiTech University, Shanghai, 201210, China; Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China; University of Chinese Academy of Sciences, Beijing 100049, China.
iHuman Institute, School of Life Science and Technology, ShanghaiTech University, Shanghai, 201210, China.
Trends Biochem Sci. 2018 Dec;43(12):1033-1046. doi: 10.1016/j.tibs.2018.09.002. Epub 2018 Oct 8.
Class Frizzled G protein-coupled receptors (GPCRs), which includes the Smoothened receptor (SMO) and 10 Frizzled receptors (FZDs), are responsible for mediating fundamental signaling in embryonic development and tissue homeostasis. Dysregulation of these receptors can lead to cancer. Structural understanding of these molecules has provided insight to their function and signaling, and guided drug discovery. To date, the structures of the multi- and individual domains of SMO, 14 FZD extracellular domains, and the transmembrane domain (TMD) of FZD4, have been reported. Here, we review all reported frizzled family structures and diverse signalosome models, with an emphasis on the different ligand binding sites and lipid binding grooves, aiming to uncover the druggability landscape of the frizzled GPCR family.
卷曲蛋白偶联受体(GPCR)家族,包括 Smoothened 受体(SMO)和 10 个卷曲受体(FZDs),负责介导胚胎发育和组织动态平衡中的基本信号转导。这些受体的失调会导致癌症。这些分子的结构理解为它们的功能和信号转导提供了线索,并指导了药物发现。迄今为止,已经报道了 SMO 的多域和单域、14 个 FZD 细胞外结构域以及 FZD4 的跨膜结构域(TMD)的结构。在这里,我们回顾了所有报道的卷曲家族结构和不同的信号转导体模型,重点介绍了不同的配体结合位点和脂质结合槽,旨在揭示卷曲 GPCR 家族的可成药性景观。