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

[Image: see text] 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 uniqu...

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Autores principales: Miller, Jonathan P., Melicher, Michael S., Schepartz, Alanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4210112/
https://www.ncbi.nlm.nih.gov/pubmed/25290247
http://dx.doi.org/10.1021/ja508872q
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author Miller, Jonathan P.
Melicher, Michael S.
Schepartz, Alanna
author_facet Miller, Jonathan P.
Melicher, Michael S.
Schepartz, Alanna
author_sort Miller, Jonathan P.
collection PubMed
description [Image: see text] 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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spelling pubmed-42101122015-10-07 Positive Allostery in Metal Ion Binding by a Cooperatively Folded β-Peptide Bundle Miller, Jonathan P. Melicher, Michael S. Schepartz, Alanna J Am Chem Soc [Image: see text] 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. American Chemical Society 2014-10-07 2014-10-22 /pmc/articles/PMC4210112/ /pubmed/25290247 http://dx.doi.org/10.1021/ja508872q Text en Copyright © 2014 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html)
spellingShingle Miller, Jonathan P.
Melicher, Michael S.
Schepartz, Alanna
Positive Allostery in Metal Ion Binding by a Cooperatively Folded β-Peptide Bundle
title Positive Allostery in Metal Ion Binding by a Cooperatively Folded β-Peptide Bundle
title_full Positive Allostery in Metal Ion Binding by a Cooperatively Folded β-Peptide Bundle
title_fullStr Positive Allostery in Metal Ion Binding by a Cooperatively Folded β-Peptide Bundle
title_full_unstemmed Positive Allostery in Metal Ion Binding by a Cooperatively Folded β-Peptide Bundle
title_short Positive Allostery in Metal Ion Binding by a Cooperatively Folded β-Peptide Bundle
title_sort positive allostery in metal ion binding by a cooperatively folded β-peptide bundle
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4210112/
https://www.ncbi.nlm.nih.gov/pubmed/25290247
http://dx.doi.org/10.1021/ja508872q
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