3PDS

Irreversible Agonist-Beta2 Adrenoceptor Complex

3PDS の概要

• エントリーDOI: 10.2210/pdb3pds/pdb
• 関連するPDBエントリー: 2RH1
• 分子名称: Fusion protein Beta-2 adrenergic receptor/Lysozyme, 8-hydroxy-5-[(1R)-1-hydroxy-2-({2-[3-methoxy-4-(3-sulfanylpropoxy)phenyl]ethyl}amino)ethyl]quinolin-2(1H)-one, CHOLESTEROL, ... (4 entities in total)
• 機能のキーワード: gpcr, signaling, beta adrenergic agonist, fusion protein, membrane protein-hydrolase complex, membrane protein/hydrolase
• 由来する生物種: Homo sapiens (human); 詳細
• 細胞内の位置: Cell membrane ; Multi- pass membrane protein : P07550
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 53860.85

構造登録者

Rosenbaum, D.M.,Zhang, C.,Lyons, J.A.,Holl, R.,Aragao, D.,Arlow, D.H.,Rasmussen, S.G.F.,Choi, H.-J.,DeVree, B.T.,Sunahara, R.K.,Chae, P.S.,Gellman, S.H.,Dror, R.O.,Shaw, D.E.,Weis, W.I.,Caffrey, M.,Gmeiner, P.,Kobilka, B.K. (登録日: 2010-10-24, 公開日: 2011-01-12, 最終更新日: 2024-10-30)

主引用文献

Rosenbaum, D.M.,Zhang, C.,Lyons, J.A.,Holl, R.,Aragao, D.,Arlow, D.H.,Rasmussen, S.G.F.,Choi, H.J.,Devree, B.T.,Sunahara, R.K.,Chae, P.S.,Gellman, S.H.,Dror, R.O.,Shaw, D.E.,Weis, W.I.,Caffrey, M.,Gmeiner, P.,Kobilka, B.K.
Structure and function of an irreversible agonist-beta(2) adrenoceptor complex
Nature, 469:236-240, 2011

PubMed Abstract: G-protein-coupled receptors (GPCRs) are eukaryotic integral membrane proteins that modulate biological function by initiating cellular signalling in response to chemically diverse agonists. Despite recent progress in the structural biology of GPCRs, the molecular basis for agonist binding and allosteric modulation of these proteins is poorly understood. Structural knowledge of agonist-bound states is essential for deciphering the mechanism of receptor activation, and for structure-guided design and optimization of ligands. However, the crystallization of agonist-bound GPCRs has been hampered by modest affinities and rapid off-rates of available agonists. Using the inactive structure of the human β(2) adrenergic receptor (β(2)AR) as a guide, we designed a β(2)AR agonist that can be covalently tethered to a specific site on the receptor through a disulphide bond. The covalent β(2)AR-agonist complex forms efficiently, and is capable of activating a heterotrimeric G protein. We crystallized a covalent agonist-bound β(2)AR-T4L fusion protein in lipid bilayers through the use of the lipidic mesophase method, and determined its structure at 3.5 Å resolution. A comparison to the inactive structure and an antibody-stabilized active structure (companion paper) shows how binding events at both the extracellular and intracellular surfaces are required to stabilize an active conformation of the receptor. The structures are in agreement with long-timescale (up to 30 μs) molecular dynamics simulations showing that an agonist-bound active conformation spontaneously relaxes to an inactive-like conformation in the absence of a G protein or stabilizing antibody.

PubMed: 21228876
DOI: 10.1038/nature09665

実験手法

X-RAY DIFFRACTION (3.5 Å)