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Crystal structure of the mitochondrial protein mitoNEET bound to a benze-sulfonide ligand

MitoNEET (gene cisd1) is a mitochondrial outer membrane [2Fe-2S] protein and is a potential drug target in several metabolic diseases. Previous studies have demonstrated that mitoNEET functions as a redox-active and pH-sensing protein that regulates mitochondrial metabolism, although the structural...

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Autores principales: Geldenhuys, Werner J., Long, Timothy E., Saralkar, Pushkar, Iwasaki, Toshio, Nuñez, Raisa A.A., Nair, Rajesh R., Konkle, Mary E., Menze, Michael A., Pinti, Mark V., Hollander, John M., Hazlehurst, Lori A., Robart, Aaron R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7205193/
https://www.ncbi.nlm.nih.gov/pubmed/32382661
http://dx.doi.org/10.1038/s42004-019-0172-x
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author Geldenhuys, Werner J.
Long, Timothy E.
Saralkar, Pushkar
Iwasaki, Toshio
Nuñez, Raisa A.A.
Nair, Rajesh R.
Konkle, Mary E.
Menze, Michael A.
Pinti, Mark V.
Hollander, John M.
Hazlehurst, Lori A.
Robart, Aaron R.
author_facet Geldenhuys, Werner J.
Long, Timothy E.
Saralkar, Pushkar
Iwasaki, Toshio
Nuñez, Raisa A.A.
Nair, Rajesh R.
Konkle, Mary E.
Menze, Michael A.
Pinti, Mark V.
Hollander, John M.
Hazlehurst, Lori A.
Robart, Aaron R.
author_sort Geldenhuys, Werner J.
collection PubMed
description MitoNEET (gene cisd1) is a mitochondrial outer membrane [2Fe-2S] protein and is a potential drug target in several metabolic diseases. Previous studies have demonstrated that mitoNEET functions as a redox-active and pH-sensing protein that regulates mitochondrial metabolism, although the structural basis of the potential drug binding site(s) remains elusive. Here we report the crystal structure of the soluble domain of human mitoNEET with a sulfonamide ligand, furosemide. Exploration of the high-resolution crystal structure is used to design mitoNEET binding molecules in a pilot study of molecular probes for use in future development of mitochondrial targeted therapies for a wide variety of metabolic diseases, including obesity, diabetes and neurodegenerative diseases such as Alzheimer’s and Parkinson’s disease.
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spelling pubmed-72051932020-05-07 Crystal structure of the mitochondrial protein mitoNEET bound to a benze-sulfonide ligand Geldenhuys, Werner J. Long, Timothy E. Saralkar, Pushkar Iwasaki, Toshio Nuñez, Raisa A.A. Nair, Rajesh R. Konkle, Mary E. Menze, Michael A. Pinti, Mark V. Hollander, John M. Hazlehurst, Lori A. Robart, Aaron R. Commun Chem Article MitoNEET (gene cisd1) is a mitochondrial outer membrane [2Fe-2S] protein and is a potential drug target in several metabolic diseases. Previous studies have demonstrated that mitoNEET functions as a redox-active and pH-sensing protein that regulates mitochondrial metabolism, although the structural basis of the potential drug binding site(s) remains elusive. Here we report the crystal structure of the soluble domain of human mitoNEET with a sulfonamide ligand, furosemide. Exploration of the high-resolution crystal structure is used to design mitoNEET binding molecules in a pilot study of molecular probes for use in future development of mitochondrial targeted therapies for a wide variety of metabolic diseases, including obesity, diabetes and neurodegenerative diseases such as Alzheimer’s and Parkinson’s disease. 2019-07-03 2019 /pmc/articles/PMC7205193/ /pubmed/32382661 http://dx.doi.org/10.1038/s42004-019-0172-x Text en http://creativecommons.org/licenses/by/4.0/ Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. Reprints and permission information is available online at http://npg.nature.com/reprintsandpermissions/
spellingShingle Article
Geldenhuys, Werner J.
Long, Timothy E.
Saralkar, Pushkar
Iwasaki, Toshio
Nuñez, Raisa A.A.
Nair, Rajesh R.
Konkle, Mary E.
Menze, Michael A.
Pinti, Mark V.
Hollander, John M.
Hazlehurst, Lori A.
Robart, Aaron R.
Crystal structure of the mitochondrial protein mitoNEET bound to a benze-sulfonide ligand
title Crystal structure of the mitochondrial protein mitoNEET bound to a benze-sulfonide ligand
title_full Crystal structure of the mitochondrial protein mitoNEET bound to a benze-sulfonide ligand
title_fullStr Crystal structure of the mitochondrial protein mitoNEET bound to a benze-sulfonide ligand
title_full_unstemmed Crystal structure of the mitochondrial protein mitoNEET bound to a benze-sulfonide ligand
title_short Crystal structure of the mitochondrial protein mitoNEET bound to a benze-sulfonide ligand
title_sort crystal structure of the mitochondrial protein mitoneet bound to a benze-sulfonide ligand
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7205193/
https://www.ncbi.nlm.nih.gov/pubmed/32382661
http://dx.doi.org/10.1038/s42004-019-0172-x
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