Surface Recognition and Parametrization of Three-Dimensional Images from Fluorescence Microscopy of Living Cells Peter Kasson Many problems in biology involve the motion of proteins on the surface of cells. One way these motions can be monitored is by labeling proteins of interest with fluorophores and then tracking motions via time-resolved three-dimensional florescence microscopy. This process generates a series of volume datasets at different time points. Most investigations conducted to date have at this point employed qualitative visual analyses (e.g. Krummel et al.). However, to carry out quantitative analysis of protein motions, we desire a surface-parametrized image for each time point rather than a field-of-view volume. Effecting such a transformation involves several stages: 1) cell identification, 2) cell tracking, 3) cell surface recognition, and 4) cell surface parametrization. These are non-trivial tasks because the cells are irregular objects that move and deform over the course of the experiments. In addition to the cell-surface motion of fluorescently labeled proteins, other confounding physical processes are fluorophore quenching, synthesis of new protein, and protein degradation. I propose to concentrate on the last two tasks in the process of analysis enumerated above: taking a volumetric image of a cell and generating first a surface and second a transformation from (x,y,z,intensity) space in the volume to (u,v,intensity) space on the surface. In this work I plan to adapt existing methods for surface reconstruction described by Zhao et al. and then devise a method for parametrization of the surfaces thus generated. References: Krummel MF, Sjaastad MD, Wulfing C, Davis MM. Differential clustering of CD4 and CD3zeta during T cell recognition. Science. 2000 Aug 25;289(5483):1349-52. Zhao, H.-K., Osher, S. and Fedkiw, R., "Fast Surface Reconstruction and Hole Filling using the Level Set Method", The 8th IEEE International Conference on Computer Vision (in press).