Cargando…

An Engineered β‐Hairpin Peptide Forming Thermostable Complexes with Zn(II), Ni(II), and Cu(II) through a His(3) Site

The three‐dimensional structure of a peptide, which determines its function, can denature at elevated temperatures, in the presence of chaotropic reagents, or in organic solvents. These factors limit the applicability of peptides. Herein, we present an engineered β‐hairpin peptide containing a His(3...

Descripción completa

Detalles Bibliográficos
Autores principales: Pham, Truc Lam, Fazliev, Sunnatullo, Baur, Philipp, Comba, Peter, Thomas, Franziska
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107957/
https://www.ncbi.nlm.nih.gov/pubmed/36445805
http://dx.doi.org/10.1002/cbic.202200588
_version_ 1785026723672227840
author Pham, Truc Lam
Fazliev, Sunnatullo
Baur, Philipp
Comba, Peter
Thomas, Franziska
author_facet Pham, Truc Lam
Fazliev, Sunnatullo
Baur, Philipp
Comba, Peter
Thomas, Franziska
author_sort Pham, Truc Lam
collection PubMed
description The three‐dimensional structure of a peptide, which determines its function, can denature at elevated temperatures, in the presence of chaotropic reagents, or in organic solvents. These factors limit the applicability of peptides. Herein, we present an engineered β‐hairpin peptide containing a His(3) site that forms complexes with Zn(II), Ni(II), and Cu(II). Circular dichroism spectroscopy shows that the peptide−metal complexes exhibit melting temperatures up to 80 °C and remain folded in 6 M guanidine hydrochloride as well as in organic solvents. Intrinsic fluorescence titration experiments were used to determine the dissociation constants of metal binding in the nano‐ to sub‐nanomolar range. The coordination geometry of the peptide−Cu(II) complex was studied by EPR spectroscopy, and a distorted square planar coordination geometry with weak interactions to axial ligands was revealed. Due to their impressive stability, the presented peptide−metal complexes open up interesting fields of application, such as the development of a new class of peptide−metal catalysts for stereoselective organic synthesis or the directed design of extremophilic β‐sheet peptides.
format Online
Article
Text
id pubmed-10107957
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-101079572023-04-18 An Engineered β‐Hairpin Peptide Forming Thermostable Complexes with Zn(II), Ni(II), and Cu(II) through a His(3) Site Pham, Truc Lam Fazliev, Sunnatullo Baur, Philipp Comba, Peter Thomas, Franziska Chembiochem Research Articles The three‐dimensional structure of a peptide, which determines its function, can denature at elevated temperatures, in the presence of chaotropic reagents, or in organic solvents. These factors limit the applicability of peptides. Herein, we present an engineered β‐hairpin peptide containing a His(3) site that forms complexes with Zn(II), Ni(II), and Cu(II). Circular dichroism spectroscopy shows that the peptide−metal complexes exhibit melting temperatures up to 80 °C and remain folded in 6 M guanidine hydrochloride as well as in organic solvents. Intrinsic fluorescence titration experiments were used to determine the dissociation constants of metal binding in the nano‐ to sub‐nanomolar range. The coordination geometry of the peptide−Cu(II) complex was studied by EPR spectroscopy, and a distorted square planar coordination geometry with weak interactions to axial ligands was revealed. Due to their impressive stability, the presented peptide−metal complexes open up interesting fields of application, such as the development of a new class of peptide−metal catalysts for stereoselective organic synthesis or the directed design of extremophilic β‐sheet peptides. John Wiley and Sons Inc. 2022-12-16 2023-02-01 /pmc/articles/PMC10107957/ /pubmed/36445805 http://dx.doi.org/10.1002/cbic.202200588 Text en © 2022 The Authors. ChemBioChem published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research Articles
Pham, Truc Lam
Fazliev, Sunnatullo
Baur, Philipp
Comba, Peter
Thomas, Franziska
An Engineered β‐Hairpin Peptide Forming Thermostable Complexes with Zn(II), Ni(II), and Cu(II) through a His(3) Site
title An Engineered β‐Hairpin Peptide Forming Thermostable Complexes with Zn(II), Ni(II), and Cu(II) through a His(3) Site
title_full An Engineered β‐Hairpin Peptide Forming Thermostable Complexes with Zn(II), Ni(II), and Cu(II) through a His(3) Site
title_fullStr An Engineered β‐Hairpin Peptide Forming Thermostable Complexes with Zn(II), Ni(II), and Cu(II) through a His(3) Site
title_full_unstemmed An Engineered β‐Hairpin Peptide Forming Thermostable Complexes with Zn(II), Ni(II), and Cu(II) through a His(3) Site
title_short An Engineered β‐Hairpin Peptide Forming Thermostable Complexes with Zn(II), Ni(II), and Cu(II) through a His(3) Site
title_sort engineered β‐hairpin peptide forming thermostable complexes with zn(ii), ni(ii), and cu(ii) through a his(3) site
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107957/
https://www.ncbi.nlm.nih.gov/pubmed/36445805
http://dx.doi.org/10.1002/cbic.202200588
work_keys_str_mv AT phamtruclam anengineeredbhairpinpeptideformingthermostablecomplexeswithzniiniiiandcuiithroughahis3site
AT fazlievsunnatullo anengineeredbhairpinpeptideformingthermostablecomplexeswithzniiniiiandcuiithroughahis3site
AT baurphilipp anengineeredbhairpinpeptideformingthermostablecomplexeswithzniiniiiandcuiithroughahis3site
AT combapeter anengineeredbhairpinpeptideformingthermostablecomplexeswithzniiniiiandcuiithroughahis3site
AT thomasfranziska anengineeredbhairpinpeptideformingthermostablecomplexeswithzniiniiiandcuiithroughahis3site
AT phamtruclam engineeredbhairpinpeptideformingthermostablecomplexeswithzniiniiiandcuiithroughahis3site
AT fazlievsunnatullo engineeredbhairpinpeptideformingthermostablecomplexeswithzniiniiiandcuiithroughahis3site
AT baurphilipp engineeredbhairpinpeptideformingthermostablecomplexeswithzniiniiiandcuiithroughahis3site
AT combapeter engineeredbhairpinpeptideformingthermostablecomplexeswithzniiniiiandcuiithroughahis3site
AT thomasfranziska engineeredbhairpinpeptideformingthermostablecomplexeswithzniiniiiandcuiithroughahis3site