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December 14, 1990Science621 citations

Acetylcholine Binding by a Synthetic Receptor: Implications for Biological Recognition

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DDDennis A. DoughertyCalifornia Institute of TechnologyDSDavid A. StaufferColumbia University

Key Points

  • This research aims to explore how a synthetic receptor binds acetylcholine and its implications for biological recognition.
  • Developed a synthetic receptor primarily made of aromatic rings.
  • Measured acetylcholine binding affinity at 50 micromolar.
  • Analyzed interactions involving cation-pi bonding.
  • The synthetic receptor binds acetylcholine with a 50-micromolar affinity.
  • Cation-pi interactions stabilize the recognition of acetylcholine's positive charge.
  • Similar binding mechanisms could play roles in the biological recognition of choline derivatives.

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.

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Cite This Study

Dougherty et al. (1990) studied this question.

synapsesocial.com/papers/69db231278a3e0e288684eadhttps://doi.org/10.1126/science.2274786
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