Cation-π interactions involving aromatic amino acids
The cation-pi interaction is a general, strong, noncovalent binding force that is used throughout nature. The side chains of the aromatic amino acids [phenylalanine (Phe), tyrosine (Tyr), and tryptophan (Trp)] provide a surface of negative electrostatic potential than can bind to a wide range of cat...
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Veröffentlicht in: | The Journal of nutrition 2007-06, Vol.137 (6S), p.1504S-1508S |
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Sprache: | eng |
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Zusammenfassung: | The cation-pi interaction is a general, strong, noncovalent binding force that is used throughout nature. The side chains of the aromatic amino acids [phenylalanine (Phe), tyrosine (Tyr), and tryptophan (Trp)] provide a surface of negative electrostatic potential than can bind to a wide range of cations through a predominantly electrostatic interaction. In this brief overview, the fundamental nature of the cation-pi interaction will be described, relying on fundamental, gas phase studies of the effect. Then, several examples of cation-pi interactions involving aromatic amino acids will be described. These include contributions to protein secondary structure, in which Phe/Tyr/Trp...lysine (Lys)/arginine interactions are common. We will also describe several examples of protein-ligand interactions that make use of cation-pi interactions. We will place special emphasis on the binding of quaternary ammonium ions, such as trimethylated Lys and the neurotransmitter acetylcholine. |
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ISSN: | 0022-3166 1541-6100 |
DOI: | 10.1093/jn/137.6.1504S |