Positive allostery in metal ion binding by a cooperatively folded β-Peptide Bundle

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Abstract

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.

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Miller, J. P., Melicher, M. S., & Schepartz, A. (2014). Positive allostery in metal ion binding by a cooperatively folded β-Peptide Bundle. Journal of the American Chemical Society, 136(42), 14726–14729. https://doi.org/10.1021/ja508872q

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