Energy homeostasis and partitioning in living cells
ORAL · Invited
Abstract
Cells consume energy to maintain activities and proliferate. A major source of energy is mitochondria, an organelle that supplies ATP for the cell. ATP is the universal energy currency of living organisms. ATP is produced through mitochondrial respiration, a metabolic process that generates ATP by consuming nutrients and oxygen. Oxygen consumption rate (OCR) of the mitochondria hence represents the metabolic activities of the cell. A key question in biology is how cells control OCR and partition ATP to power various cellular processes, including cell division, motility, biosynthesis and information procession. In this talk, I will introduce state-of-the-art techniques to measure OCR with single-cell resolution and a non-equilibrium thermodynamic model to explain energy homeostasis and partitioning in cells.
*Funding from the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under Germany's Excellence 381 Strategy – EXC-2068-390729961 – Cluster of Excellence Physics of Life of TU Dresden.
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Publication: Yang, X., Ha, G. and Needleman, D.J., 2021. A coarse-grained NADH redox model enables inference of subcellular metabolic fluxes from fluorescence lifetime imaging. Elife, 10, p.e73808.
Presenters
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Xingbo Yang
- TU Dresden