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A prochelator peptide designed to use heterometallic cooperativity to enhance metal ion affinity

A peptide has been designed so that its chelating affinity for one type of metal ion regulates its affinity for a second, different type of metal ion. The prochelator peptide (PCP), which is a fusion of motifs evocative of calcium loops and zinc fingers, forms a 1 : 2 Zn : peptide complex at pH 7.4...

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Detalles Bibliográficos
Autores principales: Alies, Bruno, Wiener, Jacob D., Franz, Katherine J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5659173/
https://www.ncbi.nlm.nih.gov/pubmed/29511523
http://dx.doi.org/10.1039/c5sc00602c
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author Alies, Bruno
Wiener, Jacob D.
Franz, Katherine J.
author_facet Alies, Bruno
Wiener, Jacob D.
Franz, Katherine J.
author_sort Alies, Bruno
collection PubMed
description A peptide has been designed so that its chelating affinity for one type of metal ion regulates its affinity for a second, different type of metal ion. The prochelator peptide (PCP), which is a fusion of motifs evocative of calcium loops and zinc fingers, forms a 1 : 2 Zn : peptide complex at pH 7.4 that increases its affinity for Zn(2+) ∼3-fold in the presence of Tb(3+) (log β(2) from 13.8 to 14.3), while the 1 : 1 luminescent complex with Tb(3+) is brighter, longer lived, and 20-fold tighter in the presence of Zn(2+) (log K from 6.2 to 7.5). This unique example of cooperative, heterometallic allostery in a biologically compatible construct suggests the possibility of designing conditionally active metal-binding agents that could respond to dynamic changes in cellular metal status.
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spelling pubmed-56591732018-03-06 A prochelator peptide designed to use heterometallic cooperativity to enhance metal ion affinity Alies, Bruno Wiener, Jacob D. Franz, Katherine J. Chem Sci Chemistry A peptide has been designed so that its chelating affinity for one type of metal ion regulates its affinity for a second, different type of metal ion. The prochelator peptide (PCP), which is a fusion of motifs evocative of calcium loops and zinc fingers, forms a 1 : 2 Zn : peptide complex at pH 7.4 that increases its affinity for Zn(2+) ∼3-fold in the presence of Tb(3+) (log β(2) from 13.8 to 14.3), while the 1 : 1 luminescent complex with Tb(3+) is brighter, longer lived, and 20-fold tighter in the presence of Zn(2+) (log K from 6.2 to 7.5). This unique example of cooperative, heterometallic allostery in a biologically compatible construct suggests the possibility of designing conditionally active metal-binding agents that could respond to dynamic changes in cellular metal status. Royal Society of Chemistry 2015-06-01 2015-05-05 /pmc/articles/PMC5659173/ /pubmed/29511523 http://dx.doi.org/10.1039/c5sc00602c Text en This journal is © The Royal Society of Chemistry 2015 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0)
spellingShingle Chemistry
Alies, Bruno
Wiener, Jacob D.
Franz, Katherine J.
A prochelator peptide designed to use heterometallic cooperativity to enhance metal ion affinity
title A prochelator peptide designed to use heterometallic cooperativity to enhance metal ion affinity
title_full A prochelator peptide designed to use heterometallic cooperativity to enhance metal ion affinity
title_fullStr A prochelator peptide designed to use heterometallic cooperativity to enhance metal ion affinity
title_full_unstemmed A prochelator peptide designed to use heterometallic cooperativity to enhance metal ion affinity
title_short A prochelator peptide designed to use heterometallic cooperativity to enhance metal ion affinity
title_sort prochelator peptide designed to use heterometallic cooperativity to enhance metal ion affinity
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5659173/
https://www.ncbi.nlm.nih.gov/pubmed/29511523
http://dx.doi.org/10.1039/c5sc00602c
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