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Article
Crystal structure of the mitochondrial protein mitoNEET bound to a benze-sulfonide ligand
Faculty Scholarship
  • Werner J. Geldenhuys, West Virginia University
  • Timothy E. Long, Marshall University
  • Pushkar Saralkar, West Virginia University
  • Toshio Iwasaki, Nippon Medical School
  • Raisa A. A. Nunez, West Virginia University
  • Rajesh R. Nair, West Virginia University
  • Mary E. Konkle, Ball State University
  • Mark V. Pinti, West Virginia University
  • Michael Menze, University of Louisville
  • John M. Hollander, West Virginia University
  • Lori A. Hazlehurst, West Virginia University
  • Aaron R. Robart, West Virginia University
Document Type
Article
Publication Date
7-3-2019
Department
Biology
Disciplines
Abstract

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.

DOI
10.1038/s42004-019-0172-x
ORCID
0000-0003-1072-5462
Citation Information

Geldenhuys, W.J., Long, T.E., Saralkar, P. et al. "Crystal structure of the mitochondrial protein mitoNEET bound to a benze-sulfonide ligand." 2019 Communications Chemistry 2, 77: 1-9.

https://doi.org/10.1038/s42004-019-0172-x