Positive Allostery in Metal Ion Binding by a Cooperatively Folded β‑Peptide Bundle

Metal ion binding is exploited by proteins in nature to catalyze reactions, bind molecules, and favor discrete structures, but it has not been demonstrated in β-peptides or their assemblies. Here we report the design, synthesis, and characterization of a β-peptide bundle that uniquely binds two Cd­(...

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Veröffentlicht in:Journal of the American Chemical Society 2014-10, Vol.136 (42), p.14726-14729
Hauptverfasser: Miller, Jonathan P, Melicher, Michael S, Schepartz, Alanna
Format: Artikel
Sprache:eng
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Zusammenfassung:Metal ion binding is exploited by proteins in nature to catalyze reactions, bind molecules, and favor discrete structures, but it has not been demonstrated in β-peptides or their assemblies. Here we report the design, synthesis, and characterization of a β-peptide bundle that uniquely binds two Cd­(II) ions in a distinct bicoordinate array. The two Cd­(II) ions bind with positive allosteric cooperativity and increase the thermodynamic stability of the bundle by more than 50 °C. This system provides a unique, synthetic context to explore allosteric regulation and should pave the way to sophisticated molecular assemblies with catalytic and substrate-sensing functions that have historically not been available to de novo designed synthetic proteomimetics in water.
ISSN:0002-7863
1520-5126
DOI:10.1021/ja508872q