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Engineering the Redox Potential over a Wide Range within a New Class of FeS Proteins
[Image: see text] MitoNEET is a newly discovered mitochondrial protein and a target of the TZD class of antidiabetes drugs. MitoNEET is homodimeric with each protomer binding a [2Fe-2S] center through a rare 3-Cys and 1-His coordination geometry. Both the fold and the coordination of the [2Fe-2S] ce...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2944382/ https://www.ncbi.nlm.nih.gov/pubmed/20812736 http://dx.doi.org/10.1021/ja103920k |
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author | Zuris, John A. Halim, Danny A. Conlan, Andrea R. Abresch, Edward C. Nechushtai, Rachel Paddock, Mark L. Jennings, Patricia A. |
author_facet | Zuris, John A. Halim, Danny A. Conlan, Andrea R. Abresch, Edward C. Nechushtai, Rachel Paddock, Mark L. Jennings, Patricia A. |
author_sort | Zuris, John A. |
collection | PubMed |
description | [Image: see text] MitoNEET is a newly discovered mitochondrial protein and a target of the TZD class of antidiabetes drugs. MitoNEET is homodimeric with each protomer binding a [2Fe-2S] center through a rare 3-Cys and 1-His coordination geometry. Both the fold and the coordination of the [2Fe-2S] centers suggest that it could have novel properties compared to other known [2Fe-2S] proteins. We tested the robustness of mitoNEET to mutation and the range over which the redox potential (E(M)) could be tuned. We found that the protein could tolerate an array of mutations that modified the E(M) of the [2Fe-2S] center over a range of ∼700 mV, which is the largest E(M) range engineered in an FeS protein and, importantly, spans the cellular redox range (+200 to −300 mV). These properties make mitoNEET potentially useful for both physiological studies and industrial applications as a stable, water-soluble, redox agent. |
format | Text |
id | pubmed-2944382 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-29443822010-09-23 Engineering the Redox Potential over a Wide Range within a New Class of FeS Proteins Zuris, John A. Halim, Danny A. Conlan, Andrea R. Abresch, Edward C. Nechushtai, Rachel Paddock, Mark L. Jennings, Patricia A. J Am Chem Soc [Image: see text] MitoNEET is a newly discovered mitochondrial protein and a target of the TZD class of antidiabetes drugs. MitoNEET is homodimeric with each protomer binding a [2Fe-2S] center through a rare 3-Cys and 1-His coordination geometry. Both the fold and the coordination of the [2Fe-2S] centers suggest that it could have novel properties compared to other known [2Fe-2S] proteins. We tested the robustness of mitoNEET to mutation and the range over which the redox potential (E(M)) could be tuned. We found that the protein could tolerate an array of mutations that modified the E(M) of the [2Fe-2S] center over a range of ∼700 mV, which is the largest E(M) range engineered in an FeS protein and, importantly, spans the cellular redox range (+200 to −300 mV). These properties make mitoNEET potentially useful for both physiological studies and industrial applications as a stable, water-soluble, redox agent. American Chemical Society 2010-09-02 2010-09-29 /pmc/articles/PMC2944382/ /pubmed/20812736 http://dx.doi.org/10.1021/ja103920k Text en Copyright © 2010 American Chemical Society http://pubs.acs.org This is an open-access article distributed under the ACS AuthorChoice Terms & Conditions. Any use of this article, must conform to the terms of that license which are available at http://pubs.acs.org. |
spellingShingle | Zuris, John A. Halim, Danny A. Conlan, Andrea R. Abresch, Edward C. Nechushtai, Rachel Paddock, Mark L. Jennings, Patricia A. Engineering the Redox Potential over a Wide Range within a New Class of FeS Proteins |
title | Engineering the Redox Potential over a Wide Range within a New Class of FeS Proteins |
title_full | Engineering the Redox Potential over a Wide Range within a New Class of FeS Proteins |
title_fullStr | Engineering the Redox Potential over a Wide Range within a New Class of FeS Proteins |
title_full_unstemmed | Engineering the Redox Potential over a Wide Range within a New Class of FeS Proteins |
title_short | Engineering the Redox Potential over a Wide Range within a New Class of FeS Proteins |
title_sort | engineering the redox potential over a wide range within a new class of fes proteins |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2944382/ https://www.ncbi.nlm.nih.gov/pubmed/20812736 http://dx.doi.org/10.1021/ja103920k |
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