Abstract

BackgroundTwo-dimensional gel electrophoresis (2DE) is a powerful technique for studying protein isoforms and their modifications. Existing commercial 2D image analysis tools rely on spot detection that limits analysis of complex protein profiles, e.g. spot appearance/disappearance or overlapping spots. Pixel-by-pixel correlation analysis, an analysis technique for identifying relations between protein patterns in gel images and external variables, can overcome such limitations in spot analysis.ResultsWe have implemented the first publically available pixel-by-pixel correlation analysis tool, the software Gel2DE. 2D immunoblot time course analysis of p53 protein stabilization in response to ionizing irradiation shows that pixel-by-pixel analysis can yield an overall activation biosignature for p53, despite changing spots shape, size and position.ConclusionsPixel-by-pixel correlation of aligned 2D images permits analysis of complex protein patterns. We anticipate that the Gel2DE correlation software will be a useful tool for future bioinformatics discoveries through 2D gel electrophoresis.

Highlights

  • Two-dimensional gel electrophoresis (2DE) is a powerful technique for studying protein isoforms and their modifications

  • We briefly review the underlying methodology in [5] on which our software is based: In a given population of individuals we wanted to study the relation between an external variable, e.g. chemotherapy to cancer cells or occupational benzene exposure to blood cells, and the isoform distribution and/or post-translational modification of a certain protein

  • The filenames of the gel images and external variables are entered into an Excel sheet that is included with the application

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Summary

Results

We have implemented the first publically available pixel-by-pixel correlation analysis tool, the software Gel2DE. 2D immunoblot time course analysis of p53 protein stabilization in response to ionizing irradiation shows that pixel-by-pixel analysis can yield an overall activation biosignature for p53, despite changing spots shape, size and position.

Conclusions
Background
Results and discussion
Conclusion

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