8J9O

Cryo-EM structure of inactive FZD1

Summary for 8J9O

• Entry DOI: 10.2210/pdb8j9o/pdb
• EMDB information: 36112
• Descriptor: Frizzled-1,Soluble cytochrome b562, anti-BRIL Fab Heavy Chain, anti-Fab nanobody, ... (4 entities in total)
• Functional Keywords: frizzled, class-f, fzd1, complex, membrane protein
• Biological source: Homo sapiens (human); More
• Total number of polymer chains: 4
• Total formula weight: 141017.64

Authors

Lin, X.,Xu, F. (deposition date: 2023-05-04, release date: 2024-01-17, Last modification date: 2025-07-02)

Primary citation

Zhang, Z.,Lin, X.,Wei, L.,Wu, Y.,Xu, L.,Wu, L.,Wei, X.,Zhao, S.,Zhu, X.,Xu, F.
A framework for Frizzled-G protein coupling and implications to the PCP signaling pathways.
Cell Discov, 10:3-3, 2024

PubMed Abstract: The ten Frizzled receptors (FZDs) are essential in Wnt signaling and play important roles in embryonic development and tumorigenesis. Among these, FZD6 is closely associated with lens development. Understanding FZD activation mechanism is key to unlock these emerging targets. Here we present the cryo-EM structures of FZD6 and FZD3 which are known to relay non-canonical planar cell polarity (PCP) signaling pathways as well as FZD1 in their G protein-coupled states and in the apo inactive states, respectively. Comparison of the three inactive/active pairs unveiled a shared activation framework among all ten FZDs. Mutagenesis along with imaging and functional analysis on the human lens epithelial tissues suggested potential crosstalk between the G-protein coupling of FZD6 and the PCP signaling pathways. Together, this study provides an integrated understanding of FZD structure and function, and lays the foundation for developing therapeutic modulators to activate or inhibit FZD signaling for a range of disorders including cancers and cataracts.

PubMed: 38182578
DOI: 10.1038/s41421-023-00627-y

Experimental method

ELECTRON MICROSCOPY (3.4 Å)