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合成受体对乙酰胆碱的结合:对生物识别的影响

Acetylcholine binding by a synthetic receptor: implications for biological recognition.

作者信息

Dougherty D A, Stauffer D A

机构信息

Arnold and Mabel Beckman Laboratories of Chemical Synthesis, California Institute of Technology, Pasadena 91125.

出版信息

Science. 1990 Dec 14;250(4987):1558-60. doi: 10.1126/science.2274786.

Abstract

The neurotransmitter acetylcholine (ACh) is bound with 50-micromolar affinity by a completely synthetic receptor (host) comprising primarily aromatic rings. The host provided an overall hydrophobic binding site, but one that could recognize the positive charge of the quaternary ammonium group of ACh through a stabilizing interaction with the electron-rich pi systems of the aromatic rings (cation-pi interaction). Similar interactions may be involved in biological recognition of ACh and other choline derivatives.

摘要

神经递质乙酰胆碱(ACh)与一种主要由芳香环组成的完全合成受体(主体)以50微摩尔的亲和力结合。该主体提供了一个整体疏水的结合位点,但它能够通过与芳香环富含电子的π体系的稳定相互作用(阳离子-π相互作用)识别ACh季铵基团的正电荷。类似的相互作用可能参与了ACh和其他胆碱衍生物的生物识别过程。

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