Reference : Assessment of Mitochondrial Cell Metabolism by Respiratory Chain Electron Flow Assays
Parts of books : Contribution to collective works
Life sciences : Biochemistry, biophysics & molecular biology
Systems Biomedicine
http://hdl.handle.net/10993/47921
Assessment of Mitochondrial Cell Metabolism by Respiratory Chain Electron Flow Assays
English
Radogna, Flavia [Laboratoire de Biologie Moléculaire et Cellulaire du Cancer]
Gerard, Déborah mailto [University of Luxembourg > Faculty of Science, Technology and Medicine (FSTM) > Department of Life Sciences and Medicine (DLSM) >]
Dicato, Mario [Laboratoire de Biologie Moléculaire et Cellulaire du Cancer]
Diederich, Marc [Seoul National University > Department of Pharmacy]
Jun-2021
Methods in Molecular Biology
Weissig, Volkmar
Edeas, Marvin
Springer
Yes
978-1-0716-1266-8
New York
United States of America
[en] Cancer Metabolism ; Mitochondrial respiration
[en] Cellular energy metabolism is regulated by complex metabolic pathways. Although anaerobic glycolysis was reported as a primary source of energy in cancer leading to a high rate of lactate production, current evidence shows that the main energy source supporting cancer cell metabolism relies on mitochondrial metabolism. Mitochondria are the key organelle maintaining optimal cellular energy levels. MitoPlate™ S-1 provides a highly reproducible bioenergetics tool to analyze the electron flow rate in live cells. Measuring the rates of electron flow into and through the electron transport chain using different NADH and FADH2-producing metabolic substrates enables the assessment of mitochondrial functionality. MitoPlate™ S-1 are 96-well microplates pre-coated with different substrates used as probes to examine the activity of mitochondrial metabolic pathways based on a colorimetric assay. A comparative metabolic analysis between cell lines or primary cells allows to establish a specific metabolic profile and to detect possible alterations of the mitochondrial function of a tumor cell. Moreover, the direct measurements of electron flux triggered by metabolic pathway activation could highlight targets for potential drug candidates.
Researchers
http://hdl.handle.net/10993/47921
10.1007/978-1-0716-1266-8_9

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