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A high-throughput assay for modulators of NNT activity in permeabilized yeast cells.

Abstract:
Nicotinamide nucleotide transhydrogenase (NNT) mutant mice show glucose intolerance with impaired insulin secretion during glucose tolerance tests. Uncoupling of the β cell mitochondrial metabolism due to such mutations makes NNT a novel target for therapeutics in the treatment of pathologies such as type 2 diabetes. The authors propose that increasing NNT activity would help reduce deleterious buildup of reactive oxygen species in the inner mitochondrial matrix. They have expressed human Nnt cDNA for the first time in Saccharomyces cerevisiae, and transhydrogenase activity in mitochondria isolated from these cells is six times greater than is seen in wild-type mitochondria. The same mitochondria have partially uncoupled respiration, and the cells have slower growth rates compared to cells that do not express NNT. The authors have used NNT's role as a redox-driven proton pump to develop a robust fluorimetric assay in permeabilized yeast. Screening in parallel a library of known pharmacologically active compounds (National Institute of Neurological Disorders and Stroke collection) against NNT ± cells, they demonstrate a robust and reproducible assay suitable for expansion into larger and more diverse compound sets. The identification of NNT activators may help in the elucidation of the role of NNT in mammalian cells and assessing its potential as a therapeutic target for insulin secretion disorders.
Publication status:
Published

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Publisher copy:
10.1177/1087057111408088

Authors


More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Physiology Anatomy & Genetics
Role:
Author


Journal:
Journal of biomolecular screening More from this journal
Volume:
16
Issue:
7
Pages:
734-743
Publication date:
2011-08-01
DOI:
EISSN:
1552-454X
ISSN:
1087-0571


Language:
English
Keywords:
Pubs id:
pubs:170232
UUID:
uuid:f2a1a2f2-7a70-4240-bbfe-ba9566a7e069
Local pid:
pubs:170232
Source identifiers:
170232
Deposit date:
2012-12-19

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