Paper
19 February 2007 Development of automatic image analysis algorithms for protein localization studies in budding yeast
Katarina Logg, Mats Kvarnström, Alfredo Diez, Kristofer Bodvard, Mikael Käll
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Abstract
Microscopy of fluorescently labeled proteins has become a standard technique for live cell imaging. However, it is still a challenge to systematically extract quantitative data from large sets of images in an unbiased fashion, which is particularly important in high-throughput or time-lapse studies. Here we describe the development of a software package aimed at automatic quantification of abundance and spatio-temporal dynamics of fluorescently tagged proteins in vivo in the budding yeast Saccharomyces cerevisiae, one of the most important model organisms in proteomics. The image analysis methodology is based on first identifying cell contours from bright field images, and then use this information to measure and statistically analyse protein abundance in specific cellular domains from the corresponding fluorescence images. The applicability of the procedure is exemplified for two nuclear localized GFP-tagged proteins, Mcm4p and Nrm1p.
© (2007) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Katarina Logg, Mats Kvarnström, Alfredo Diez, Kristofer Bodvard, and Mikael Käll "Development of automatic image analysis algorithms for protein localization studies in budding yeast", Proc. SPIE 6441, Imaging, Manipulation, and Analysis of Biomolecules, Cells, and Tissues V, 64411J (19 February 2007); https://doi.org/10.1117/12.700179
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Cited by 1 scholarly publication.
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KEYWORDS
Proteins

Image segmentation

Luminescence

Algorithm development

Image analysis

Yeast

Detection and tracking algorithms

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