2UZ6

AChBP-targeted a-conotoxin correlates distinct binding orientations with nAChR subtype selectivity.

2UZ6 の概要

• エントリーDOI: 10.2210/pdb2uz6/pdb
• 関連するPDBエントリー: 2BR7 2BR8 2BYN 2BYP 2BYQ 2BYR 2BYS 2C9T
• 分子名称: SOLUBLE ACETYLCHOLINE RECEPTOR, ALPHA-CONOTOXIN TXIA(A10L), 2-acetamido-2-deoxy-beta-D-glucopyranose, ... (5 entities in total)
• 機能のキーワード: receptor-toxin complex, receptor/toxin
• 由来する生物種: APLYSIA CALIFORNICA; 詳細
• タンパク質・核酸の鎖数: 20
• 化学式量合計: 264552.67

構造登録者

Ulens, C.,Dutertre, S.,Buttner, R.,Fish, A.,van Elk, R.,Kendel, Y.,Hopping, G.,Alewood, P.F.,Schroeder, C.,Nicke, A.,Smit, A.B.,Sixma, T.K.,Lewis, R.J. (登録日: 2007-04-25, 公開日: 2007-08-07, 最終更新日: 2024-10-23)

主引用文献

Dutertre, S.,Ulens, C.,Buttner, R.,Fish, A.,Van Elk, R.,Kendel, Y.,Hopping, G.,Alewood, P.F.,Schroeder, C.,Nicke, A.,Smit, A.B.,Sixma, T.K.,Lewis, R.J.
Achbp-Targeted Alpha-Conotoxin Correlates Distinct Binding Orientations with Nachr Subtype Selectivity
Embo J., 26:3858-, 2007

PubMed Abstract: Neuronal nAChRs are a diverse family of pentameric ion channels with wide distribution throughout cells of the nervous and immune systems. However, the role of specific subtypes in normal and pathological states remains poorly understood due to the lack of selective probes. Here, we used a binding assay based on acetylcholine-binding protein (AChBP), a homolog of the nicotinic acetylcholine ligand-binding domain, to discover a novel alpha-conotoxin (alpha-TxIA) in the venom of Conus textile. Alpha-TxIA bound with high affinity to AChBPs from different species and selectively targeted the alpha(3)beta(2) nAChR subtype. A co-crystal structure of Ac-AChBP with the enhanced potency analog TxIA(A10L), revealed a 20 degrees backbone tilt compared to other AChBP-conotoxin complexes. This reorientation was coordinated by a key salt bridge formed between Arg5 (TxIA) and Asp195 (Ac-AChBP). Mutagenesis studies, biochemical assays and electrophysiological recordings directly correlated the interactions observed in the co-crystal structure to binding affinity at AChBP and different nAChR subtypes. Together, these results establish a new pharmacophore for the design of novel subtype-selective ligands with therapeutic potential in nAChR-related diseases.

PubMed: 17660751
DOI: 10.1038/SJ.EMBOJ.7601785

実験手法

X-RAY DIFFRACTION (2.4 Å)