9UTA
The transmembrane domains of human sweet taste receptor TAS1R2 and TAS1R3 in the apo state
9UTA の概要
| エントリーDOI | 10.2210/pdb9uta/pdb |
| EMDBエントリー | 64486 |
| 分子名称 | Taste receptor type 1 member 2,Engineered red fluorescent protein mScarlet3, Taste receptor type 1 member 3,mNeonGreen (2 entities in total) |
| 機能のキーワード | gpcr, taste, tas1r2, tas1r3, signaling protein |
| 由来する生物種 | Homo sapiens (human) 詳細 |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 247097.83 |
| 構造登録者 | |
| 主引用文献 | Shi, Z.,Xu, W.,Wu, L.,Yue, X.,Liu, S.,Ding, W.,Zhang, J.,Meng, B.,Zhao, L.,Liu, X.,Liu, J.,Liu, Z.J.,Hua, T. Structural and functional characterization of human sweet taste receptor. Nature, 645:801-808, 2025 Cited by PubMed Abstract: Sweet taste perception influences dietary choices and metabolic health. The human sweet taste receptor, a class C G-protein-coupled receptor (GPCR) heterodimer composed of TAS1R2 and TAS1R3 (refs. ), senses a wide range of sweet compounds-including natural sugars, artificial sweeteners and sweet proteins-and affects metabolic regulation beyond taste. However, the lack of three-dimensional structures hinders our understanding of its precise working mechanism. Here we present cryo-electron microscopy structures of the full-length human sweet taste receptor in apo and sucralose-bound states. These structures reveal a distinct asymmetric heterodimer architecture, with sucralose binding exclusively to the Venus flytrap domain of TAS1R2. Combining mutagenesis and molecular dynamics simulations, this work delineates the sweetener-recognition modes in TAS1R2. Structural comparisons further uncover conformational changes upon ligand binding and a unique activation mechanism. These findings illuminate the signal transduction mechanisms of chemosensory receptors in the class C GPCR family and provide the molecular basis for the design of a new generation of sweeteners. PubMed: 40555359DOI: 10.1038/s41586-025-09302-6 主引用文献が同じPDBエントリー |
| 実験手法 | ELECTRON MICROSCOPY (3.77 Å) |
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