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Integrated Computational Approach to the Electron Paramagnetic Resonance Characterization of Rigid 3(10)-Helical Peptides with TOAC Nitroxide Spin Labels
[Image: see text] We address the interpretation, via an integrated computational approach, of the experimental continuous-wave electron paramagnetic resonance (cw-EPR) spectra of a complete set of conformationally highly restricted, stable 3(10)-helical peptides from hexa- to nonamers, each bis-labe...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5628910/ https://www.ncbi.nlm.nih.gov/pubmed/28422504 http://dx.doi.org/10.1021/acs.jpcb.7b01050 |
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author | Gerolin, Marco Zerbetto, Mirco Moretto, Alessandro Formaggio, Fernando Toniolo, Claudio van Son, Martin Shabestari, Maryam Hashemi Huber, Martina Calligari, Paolo Polimeno, Antonino |
author_facet | Gerolin, Marco Zerbetto, Mirco Moretto, Alessandro Formaggio, Fernando Toniolo, Claudio van Son, Martin Shabestari, Maryam Hashemi Huber, Martina Calligari, Paolo Polimeno, Antonino |
author_sort | Gerolin, Marco |
collection | PubMed |
description | [Image: see text] We address the interpretation, via an integrated computational approach, of the experimental continuous-wave electron paramagnetic resonance (cw-EPR) spectra of a complete set of conformationally highly restricted, stable 3(10)-helical peptides from hexa- to nonamers, each bis-labeled with nitroxide radical-containing TOAC (4-amino-1-oxyl-2,2,6,6-tetramethylpiperidine-4-carboxylic acid) residues. The usefulness of TOAC for this type of analysis has been shown already to be due to its cyclic piperidine side chain, which is rigidly connected to the peptide backbone α-carbon. The TOAC α-amino acids are separated by two, three, four, and five intervening residues. This set of compounds has allowed us to modulate both the radical···radical distance and the relative orientation parameters. To further validate our conclusion, a comparative analysis has been carried out on three singly TOAC-labeled peptides of similar main-chain length. |
format | Online Article Text |
id | pubmed-5628910 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-56289102017-10-06 Integrated Computational Approach to the Electron Paramagnetic Resonance Characterization of Rigid 3(10)-Helical Peptides with TOAC Nitroxide Spin Labels Gerolin, Marco Zerbetto, Mirco Moretto, Alessandro Formaggio, Fernando Toniolo, Claudio van Son, Martin Shabestari, Maryam Hashemi Huber, Martina Calligari, Paolo Polimeno, Antonino J Phys Chem B [Image: see text] We address the interpretation, via an integrated computational approach, of the experimental continuous-wave electron paramagnetic resonance (cw-EPR) spectra of a complete set of conformationally highly restricted, stable 3(10)-helical peptides from hexa- to nonamers, each bis-labeled with nitroxide radical-containing TOAC (4-amino-1-oxyl-2,2,6,6-tetramethylpiperidine-4-carboxylic acid) residues. The usefulness of TOAC for this type of analysis has been shown already to be due to its cyclic piperidine side chain, which is rigidly connected to the peptide backbone α-carbon. The TOAC α-amino acids are separated by two, three, four, and five intervening residues. This set of compounds has allowed us to modulate both the radical···radical distance and the relative orientation parameters. To further validate our conclusion, a comparative analysis has been carried out on three singly TOAC-labeled peptides of similar main-chain length. American Chemical Society 2017-04-19 2017-05-04 /pmc/articles/PMC5628910/ /pubmed/28422504 http://dx.doi.org/10.1021/acs.jpcb.7b01050 Text en Copyright © 2017 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Gerolin, Marco Zerbetto, Mirco Moretto, Alessandro Formaggio, Fernando Toniolo, Claudio van Son, Martin Shabestari, Maryam Hashemi Huber, Martina Calligari, Paolo Polimeno, Antonino Integrated Computational Approach to the Electron Paramagnetic Resonance Characterization of Rigid 3(10)-Helical Peptides with TOAC Nitroxide Spin Labels |
title | Integrated Computational Approach
to the Electron
Paramagnetic Resonance Characterization of Rigid 3(10)-Helical
Peptides with TOAC Nitroxide Spin Labels |
title_full | Integrated Computational Approach
to the Electron
Paramagnetic Resonance Characterization of Rigid 3(10)-Helical
Peptides with TOAC Nitroxide Spin Labels |
title_fullStr | Integrated Computational Approach
to the Electron
Paramagnetic Resonance Characterization of Rigid 3(10)-Helical
Peptides with TOAC Nitroxide Spin Labels |
title_full_unstemmed | Integrated Computational Approach
to the Electron
Paramagnetic Resonance Characterization of Rigid 3(10)-Helical
Peptides with TOAC Nitroxide Spin Labels |
title_short | Integrated Computational Approach
to the Electron
Paramagnetic Resonance Characterization of Rigid 3(10)-Helical
Peptides with TOAC Nitroxide Spin Labels |
title_sort | integrated computational approach
to the electron
paramagnetic resonance characterization of rigid 3(10)-helical
peptides with toac nitroxide spin labels |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5628910/ https://www.ncbi.nlm.nih.gov/pubmed/28422504 http://dx.doi.org/10.1021/acs.jpcb.7b01050 |
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