A computational model for mitochondrial function has been developed from oxygen concentration data measured in the Oroboros Oxygraph-2k and oxygen consumption rates measured in the Seahorse XF24 Analyzer. Measurements were acquired using embryonic-cultured cortical neurons and isolated mitochondria from CD1 mice. Based on the biological mechanism of mitochondrial activity, a computational model was developed using biochemical kinetic modelling. To modulate mitochondrial activity, dysfunctions were introduced by injecting the inhibiting reagents oligomycin, rotenone, and antimycin A, and the uncoupling reagent carbonyl cyanide 4-(trifluoromethoxy)phenylhydrazone (FCCP) during measurements. To incorporate these changes, model equations were adapted and globally calibrated to experimental data using the genetic algorithm developed by Jason Fiege of the University of Manitoba by fitting oxygen concentration data. The model was coded in MATLAB R2014a along with the development of a graphical user interface for simulating mitochondrial bioenergetics in silico. / October 2016
| Identifer | oai:union.ndltd.org:MANITOBA/oai:mspace.lib.umanitoba.ca:1993/31602 |
| Date | 24 August 2016 |
| Creators | Cadonic, Chris |
| Contributors | Albensi, Benedict (Pharmacology And Therapeutics) Portet, Stephanie (Mathematics), Thomson, Douglas (Electrical & Computer Engineering) Amara, Francis (Biochemistry & Medical Genetics) Treberg, Jason (Biological Sciences) |
| Source Sets | University of Manitoba Canada |
| Detected Language | English |
Page generated in 0.0034 seconds