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Synthetic receptors as models for alkali metal cation-[Pi] binding sites in proteins
- Source :
- Proceedings of the National Academy of Sciences of the United States. June 6, 2000, Vol. 97 Issue 12, 6271
- Publication Year :
- 2000
-
Abstract
- The alkali metal cations [Na.sup.+] and [K.sup.+] have several important physiological roles, including modulating enzyme activity. Recent work has suggested that alkali metal cations may be coordinated by [Pi] systems, such as the aromatic amino acid side chains. The ability of [K.sup.+] to interact with an aromatic ring has been assessed by preparing a family of synthetic receptors that incorporate the aromatic side chains of phenylalanine, tyrosine, and tryptophan. These receptors are constructed around a diaza-18-crown-6 scaffold, which serves as the primary binding site for an alkali metal cation. The ability of the aromatic rings to coordinate a cation was determined by crystallizing each of the receptors in the presence of [K.sup.+] and by solving the solid state structures. In all cases, complexation of [K.sup.+] by the [Pi] system was observed. When possible, the structures of the unbound receptors also were determined for comparison. Further proof that the aromatic ring makes an energetically favorable interaction with the cation was obtained by preparing a receptor in which the arene was perfluorinated. Fluorination of the arene reverses the electrostatics, but the aromaticity is maintained. The fluorinated arene rings do not coordinate the cation in the solid state structure of the [K.sup.+] complex. Thus, the results of the predicted electrostatic reversal were confirmed. Finally, the biological implications of the alkali metal cation-[Pi] interaction are addressed.
Details
- ISSN :
- 00278424
- Volume :
- 97
- Issue :
- 12
- Database :
- Gale General OneFile
- Journal :
- Proceedings of the National Academy of Sciences of the United States
- Publication Type :
- Academic Journal
- Accession number :
- edsgcl.63126971