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Positive Allostery in Metal Ion Binding by a Cooperatively Folded β-Peptide Bundle
Author(s) -
Jonathan P. Miller,
Michael S. Melicher,
Alanna Schepartz
Publication year - 2014
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/ja508872q
Subject(s) - chemistry , allosteric regulation , cooperativity , context (archaeology) , peptide , bundle , cooperative binding , combinatorial chemistry , substrate (aquarium) , metal ions in aqueous solution , molecule , stereochemistry , ion , biophysics , binding site , biochemistry , enzyme , organic chemistry , paleontology , materials science , oceanography , composite material , biology , geology
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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