7D68
Cryo-EM structure of the human glucagon-like peptide-2 receptor-Gs protein complex
Summary for 7D68
Entry DOI | 10.2210/pdb7d68/pdb |
EMDB information | 30590 |
Descriptor | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short, Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2, ... (7 entities in total) |
Functional Keywords | glucagon-like peptide-2 receptor, drug target, class b gpcr, biosynthetic protein |
Biological source | Bos taurus More |
Total number of polymer chains | 6 |
Total formula weight | 185001.18 |
Authors | |
Primary citation | Sun, W.,Chen, L.N.,Zhou, Q.,Zhao, L.H.,Yang, D.,Zhang, H.,Cong, Z.,Shen, D.D.,Zhao, F.,Zhou, F.,Cai, X.,Chen, Y.,Zhou, Y.,Gadgaard, S.,van der Velden, W.J.C.,Zhao, S.,Jiang, Y.,Rosenkilde, M.M.,Xu, H.E.,Zhang, Y.,Wang, M.W. A unique hormonal recognition feature of the human glucagon-like peptide-2 receptor. Cell Res., 30:1098-1108, 2020 Cited by PubMed Abstract: Glucagon-like peptides (GLP-1 and GLP-2) are two proglucagon-derived intestinal hormones that mediate distinct physiological functions through two related receptors (GLP-1R and GLP-2R) which are important drug targets for metabolic disorders and Crohn's disease, respectively. Despite great progress in GLP-1R structure determination, our understanding on the differences of peptide binding and signal transduction between these two receptors remains elusive. Here we report the electron microscopy structure of the human GLP-2R in complex with GLP-2 and a G heterotrimer. To accommodate GLP-2 rather than GLP-1, GLP-2R fine-tunes the conformations of the extracellular parts of transmembrane helices (TMs) 1, 5, 7 and extracellular loop 1 (ECL1). In contrast to GLP-1, the N-terminal histidine of GLP-2 penetrates into the receptor core with a unique orientation. The middle region of GLP-2 engages with TM1 and TM7 more extensively than with ECL2, and the GLP-2 C-terminus closely attaches to ECL1, which is the most protruded among 9 class B G protein-coupled receptors (GPCRs). Functional studies revealed that the above three segments of GLP-2 are essential for GLP-2 recognition and receptor activation, especially the middle region. These results provide new insights into the molecular basis of ligand specificity in class B GPCRs and may facilitate the development of more specific therapeutics. PubMed: 33239759DOI: 10.1038/s41422-020-00442-0 PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (3 Å) |
Structure validation
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