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gem‐Diethyl Pyrroline Nitroxide Spin Labels: Synthesis, EPR Characterization, Rotamer Libraries and Biocompatibility
The availability of bioresistant spin labels is crucial for the optimization of site‐directed spin labeling protocols for EPR structural studies of biomolecules in a cellular context. As labeling can affect proteins’ fold and/or function, having the possibility to choose between different spin label...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709561/ https://www.ncbi.nlm.nih.gov/pubmed/31463171 http://dx.doi.org/10.1002/open.201900119 |
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author | Bleicken, Stephanie Assafa, Tufa E. Zhang, Hui Elsner, Christina Ritsch, Irina Pink, Maren Rajca, Suchada Jeschke, Gunnar Rajca, Andrzej Bordignon, Enrica |
author_facet | Bleicken, Stephanie Assafa, Tufa E. Zhang, Hui Elsner, Christina Ritsch, Irina Pink, Maren Rajca, Suchada Jeschke, Gunnar Rajca, Andrzej Bordignon, Enrica |
author_sort | Bleicken, Stephanie |
collection | PubMed |
description | The availability of bioresistant spin labels is crucial for the optimization of site‐directed spin labeling protocols for EPR structural studies of biomolecules in a cellular context. As labeling can affect proteins’ fold and/or function, having the possibility to choose between different spin labels will increase the probability to produce spin‐labeled functional proteins. Here, we report the synthesis and characterization of iodoacetamide‐ and maleimide‐functionalized spin labels based on the gem‐diethyl pyrroline structure. The two nitroxide labels are compared to conventional gem‐dimethyl analogs by site‐directed spin labeling (SDSL) electron paramagnetic resonance (EPR) spectroscopy, using two water soluble proteins: T4 lysozyme and Bid. To foster their use for structural studies, we also present rotamer libraries for these labels, compatible with the MMM software. Finally, we investigate the “true” biocompatibility of the gem‐diethyl probes comparing the resistance towards chemical reduction of the NO group in ascorbate solutions and E. coli cytosol at different spin concentrations. |
format | Online Article Text |
id | pubmed-6709561 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67095612019-08-28 gem‐Diethyl Pyrroline Nitroxide Spin Labels: Synthesis, EPR Characterization, Rotamer Libraries and Biocompatibility Bleicken, Stephanie Assafa, Tufa E. Zhang, Hui Elsner, Christina Ritsch, Irina Pink, Maren Rajca, Suchada Jeschke, Gunnar Rajca, Andrzej Bordignon, Enrica ChemistryOpen Full Papers The availability of bioresistant spin labels is crucial for the optimization of site‐directed spin labeling protocols for EPR structural studies of biomolecules in a cellular context. As labeling can affect proteins’ fold and/or function, having the possibility to choose between different spin labels will increase the probability to produce spin‐labeled functional proteins. Here, we report the synthesis and characterization of iodoacetamide‐ and maleimide‐functionalized spin labels based on the gem‐diethyl pyrroline structure. The two nitroxide labels are compared to conventional gem‐dimethyl analogs by site‐directed spin labeling (SDSL) electron paramagnetic resonance (EPR) spectroscopy, using two water soluble proteins: T4 lysozyme and Bid. To foster their use for structural studies, we also present rotamer libraries for these labels, compatible with the MMM software. Finally, we investigate the “true” biocompatibility of the gem‐diethyl probes comparing the resistance towards chemical reduction of the NO group in ascorbate solutions and E. coli cytosol at different spin concentrations. John Wiley and Sons Inc. 2019-05-14 /pmc/articles/PMC6709561/ /pubmed/31463171 http://dx.doi.org/10.1002/open.201900119 Text en © 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Full Papers Bleicken, Stephanie Assafa, Tufa E. Zhang, Hui Elsner, Christina Ritsch, Irina Pink, Maren Rajca, Suchada Jeschke, Gunnar Rajca, Andrzej Bordignon, Enrica gem‐Diethyl Pyrroline Nitroxide Spin Labels: Synthesis, EPR Characterization, Rotamer Libraries and Biocompatibility |
title |
gem‐Diethyl Pyrroline Nitroxide Spin Labels: Synthesis, EPR Characterization, Rotamer Libraries and Biocompatibility |
title_full |
gem‐Diethyl Pyrroline Nitroxide Spin Labels: Synthesis, EPR Characterization, Rotamer Libraries and Biocompatibility |
title_fullStr |
gem‐Diethyl Pyrroline Nitroxide Spin Labels: Synthesis, EPR Characterization, Rotamer Libraries and Biocompatibility |
title_full_unstemmed |
gem‐Diethyl Pyrroline Nitroxide Spin Labels: Synthesis, EPR Characterization, Rotamer Libraries and Biocompatibility |
title_short |
gem‐Diethyl Pyrroline Nitroxide Spin Labels: Synthesis, EPR Characterization, Rotamer Libraries and Biocompatibility |
title_sort | gem‐diethyl pyrroline nitroxide spin labels: synthesis, epr characterization, rotamer libraries and biocompatibility |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709561/ https://www.ncbi.nlm.nih.gov/pubmed/31463171 http://dx.doi.org/10.1002/open.201900119 |
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