Geissbühler, MatthiasSpielmann, ThiemoFormey de Saint Louvent, AurélieMärki, IwanLeutenegger, MarcelHinz, BorisJohnsson, Kaivan De Ville, DimitriLasser, Theo2012-02-242012-02-24201210.1007/978-1-4614-1566-4_39https://infoscience.epfl.ch/handle/20.500.14299/78085WOS:000313161700040Triplet imaging is a novel optical technique that allows investigating oxy- gen metabolism at the single cell and the sub-cellular level. The method combines high temporal and spatial resolution, which are required for the monitoring of fast kinetics of oxygen concentration in living cells. Calibration and validation is demon- strated with a titration experiment using L-Ascorbic Acid with the enzyme Ascor- base oxidase. The method was applied to a biological cell system, employing as reporter a cytosolic fusion protein of β-galactosidase with SNAP-tag labeled with tetramethylrhodamine. Oxygen consumption in single smooth muscle cells A7r5 during an [Arg8]-vasopressin-induced contraction is measured. The results indicate a consumption leading to an intracellular oxygen concentration that decays mono- exponentially with time. This is in good agreement with previously reported mea- surements of oxygen consumption in skeletal muscle fibers.Triplet imaging of oxygen consumption during the contraction of a single smooth muscle cell (A7r5)text::conference output::conference proceedings::conference paper