8HSC
Gi bound Orphan GPR20 complex with Fab046 in ligand-free state
8HSC の概要
エントリーDOI | 10.2210/pdb8hsc/pdb |
EMDBエントリー | 34993 |
分子名称 | light chain of Fab046, Guanine nucleotide-binding protein G(i) subunit alpha-1, Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, ... (7 entities in total) |
機能のキーワード | orphan receptor, gpcr, gpr20, gi-coupled, gpr20-gi-fab046, membrane protein |
由来する生物種 | Rattus 詳細 |
タンパク質・核酸の鎖数 | 7 |
化学式量合計 | 224707.03 |
構造登録者 | |
主引用文献 | Lin, X.,Jiang, S.,Wu, Y.,Wei, X.,Han, G.W.,Wu, L.,Liu, J.,Chen, B.,Zhang, Z.,Zhao, S.,Cherezov, V.,Xu, F. The activation mechanism and antibody binding mode for orphan GPR20. Cell Discov, 9:23-23, 2023 Cited by PubMed Abstract: GPR20 is a class-A orphan G protein-coupled receptor (GPCR) and a potential therapeutic target for gastrointestinal stromal tumors (GIST) owing to its differentially high expression. An antibody-drug conjugate (ADC) containing a GPR20-binding antibody (Ab046) was recently developed in clinical trials for GIST treatment. GPR20 constitutively activates Gi proteins in the absence of any known ligand, but it remains obscure how this high basal activity is achieved. Here we report three cryo-EM structures of human GPR20 complexes including Gi-coupled GPR20 in the absence or presence of the Fab fragment of Ab046 and Gi-free GPR20. Remarkably, the structures demonstrate a uniquely folded N-terminal helix capping onto the transmembrane domain and our mutagenesis study suggests a key role of this cap region in stimulating the basal activity of GPR20. We also uncover the molecular interactions between GPR20 and Ab046, which may enable the design of tool antibodies with enhanced affinity or new functionality for GPR20. Furthermore, we report the orthosteric pocket occupied by an unassigned density which might be essential for exploring opportunities for deorphanization. PubMed: 36849514DOI: 10.1038/s41421-023-00520-8 主引用文献が同じPDBエントリー |
実験手法 | ELECTRON MICROSCOPY (3.22 Å) |
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