3NEQ

Crystal structure of the chimeric muscarinic toxin MT7 with loop 3 from MT1

3NEQ の概要

• エントリーDOI: 10.2210/pdb3neq/pdb
• 関連するPDBエントリー: 1FF4 2VLW 3FEV
• 分子名称: Three-finger muscarinic toxin 7, SULFATE ION (3 entities in total)
• 機能のキーワード: chimeric muscarinic toxin, hm1-muscarinic receptor, snake toxin, green mamba, toxin
• 由来する生物種: Dendroaspis angusticeps (Eastern green mamba); 詳細
• 細胞内の位置: Secreted : Q8QGR0
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 15577.72

構造登録者

Stura, E.A.,Servent, D.,Menez, R.,Mournier, G.,Menez, A.,Fruchart-Gaillard, C. (登録日: 2010-06-09, 公開日: 2011-08-24, 最終更新日: 2023-09-06)

主引用文献

Fruchart-Gaillard, C.,Mourier, G.,Blanchet, G.,Vera, L.,Gilles, N.,Menez, R.,Marcon, E.,Stura, E.A.,Servent, D.
Engineering of three-finger fold toxins creates ligands with original pharmacological profiles for muscarinic and adrenergic receptors.
Plos One, 7:e39166-e39166, 2012

PubMed Abstract: Protein engineering approaches are often a combination of rational design and directed evolution using display technologies. Here, we test "loop grafting," a rational design method, on three-finger fold proteins. These small reticulated proteins have exceptional affinity and specificity for their diverse molecular targets, display protease-resistance, and are highly stable and poorly immunogenic. The wealth of structural knowledge makes them good candidates for protein engineering of new functionality. Our goal is to enhance the efficacy of these mini-proteins by modifying their pharmacological properties in order to extend their use in imaging, diagnostics and therapeutic applications. Using the interaction of three-finger fold toxins with muscarinic and adrenergic receptors as a model, chimeric toxins have been engineered by substituting loops on toxin MT7 by those from toxin MT1. The pharmacological impact of these grafts was examined using binding experiments on muscarinic receptors M1 and M4 and on the α(1A)-adrenoceptor. Some of the designed chimeric proteins have impressive gain of function on certain receptor subtypes achieving an original selectivity profile with high affinity for muscarinic receptor M1 and α(1A)-adrenoceptor. Structure-function analysis supported by crystallographic data for MT1 and two chimeras permits a molecular based interpretation of these gains and details the merits of this protein engineering technique. The results obtained shed light on how loop permutation can be used to design new three-finger proteins with original pharmacological profiles.

PubMed: 22720062
DOI: 10.1371/journal.pone.0039166

実験手法

X-RAY DIFFRACTION (1.25 Å)