Cargando…
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...
Autores principales: | , , |
---|---|
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 |
_version_ | 1782341324959121408 |
---|---|
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. |
format | Online Article Text |
id | pubmed-4210112 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT millerjonathanp positiveallosteryinmetalionbindingbyacooperativelyfoldedbpeptidebundle AT melichermichaels positiveallosteryinmetalionbindingbyacooperativelyfoldedbpeptidebundle AT schepartzalanna positiveallosteryinmetalionbindingbyacooperativelyfoldedbpeptidebundle |