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Correlation analysis of two-dimensional gel electrophoretic protein patterns and biological variables

BACKGROUND: Two-dimensional gel electrophoresis (2DE) is a powerful technique to examine post-translational modifications of complexly modulated proteins. Currently, spot detection is a necessary step to assess relations between spots and biological variables. This often proves time consuming and di...

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Autores principales: Van Belle, Werner, Ånensen, Nina, Haaland, Ingvild, Bruserud, Øystein, Høgda, Kjell-Arild, Gjertsen, Bjørn Tore
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1559651/
https://www.ncbi.nlm.nih.gov/pubmed/16606449
http://dx.doi.org/10.1186/1471-2105-7-198
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author Van Belle, Werner
Ånensen, Nina
Haaland, Ingvild
Bruserud, Øystein
Høgda, Kjell-Arild
Gjertsen, Bjørn Tore
author_facet Van Belle, Werner
Ånensen, Nina
Haaland, Ingvild
Bruserud, Øystein
Høgda, Kjell-Arild
Gjertsen, Bjørn Tore
author_sort Van Belle, Werner
collection PubMed
description BACKGROUND: Two-dimensional gel electrophoresis (2DE) is a powerful technique to examine post-translational modifications of complexly modulated proteins. Currently, spot detection is a necessary step to assess relations between spots and biological variables. This often proves time consuming and difficult when working with non-perfect gels. We developed an analysis technique to measure correlation between 2DE images and biological variables on a pixel by pixel basis. After image alignment and normalization, the biological parameters and pixel values are replaced by their specific rank. These rank adjusted images and parameters are then put into a standard linear Pearson correlation and further tested for significance and variance. RESULTS: We validated this technique on a set of simulated 2DE images, which revealed also correct working under the presence of normalization factors. This was followed by an analysis of p53 2DE immunoblots from cancer cells, known to have unique signaling networks. Since p53 is altered through these signaling networks, we expected to find correlations between the cancer type (acute lymphoblastic leukemia and acute myeloid leukemia) and the p53 profiles. A second correlation analysis revealed a more complex relation between the differentiation stage in acute myeloid leukemia and p53 protein isoforms. CONCLUSION: The presented analysis method measures relations between 2DE images and external variables without requiring spot detection, thereby enabling the exploration of biosignatures of complex signaling networks in biological systems.
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spelling pubmed-15596512006-09-08 Correlation analysis of two-dimensional gel electrophoretic protein patterns and biological variables Van Belle, Werner Ånensen, Nina Haaland, Ingvild Bruserud, Øystein Høgda, Kjell-Arild Gjertsen, Bjørn Tore BMC Bioinformatics Methodology Article BACKGROUND: Two-dimensional gel electrophoresis (2DE) is a powerful technique to examine post-translational modifications of complexly modulated proteins. Currently, spot detection is a necessary step to assess relations between spots and biological variables. This often proves time consuming and difficult when working with non-perfect gels. We developed an analysis technique to measure correlation between 2DE images and biological variables on a pixel by pixel basis. After image alignment and normalization, the biological parameters and pixel values are replaced by their specific rank. These rank adjusted images and parameters are then put into a standard linear Pearson correlation and further tested for significance and variance. RESULTS: We validated this technique on a set of simulated 2DE images, which revealed also correct working under the presence of normalization factors. This was followed by an analysis of p53 2DE immunoblots from cancer cells, known to have unique signaling networks. Since p53 is altered through these signaling networks, we expected to find correlations between the cancer type (acute lymphoblastic leukemia and acute myeloid leukemia) and the p53 profiles. A second correlation analysis revealed a more complex relation between the differentiation stage in acute myeloid leukemia and p53 protein isoforms. CONCLUSION: The presented analysis method measures relations between 2DE images and external variables without requiring spot detection, thereby enabling the exploration of biosignatures of complex signaling networks in biological systems. BioMed Central 2006-04-10 /pmc/articles/PMC1559651/ /pubmed/16606449 http://dx.doi.org/10.1186/1471-2105-7-198 Text en Copyright © 2006 Van Belle et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methodology Article
Van Belle, Werner
Ånensen, Nina
Haaland, Ingvild
Bruserud, Øystein
Høgda, Kjell-Arild
Gjertsen, Bjørn Tore
Correlation analysis of two-dimensional gel electrophoretic protein patterns and biological variables
title Correlation analysis of two-dimensional gel electrophoretic protein patterns and biological variables
title_full Correlation analysis of two-dimensional gel electrophoretic protein patterns and biological variables
title_fullStr Correlation analysis of two-dimensional gel electrophoretic protein patterns and biological variables
title_full_unstemmed Correlation analysis of two-dimensional gel electrophoretic protein patterns and biological variables
title_short Correlation analysis of two-dimensional gel electrophoretic protein patterns and biological variables
title_sort correlation analysis of two-dimensional gel electrophoretic protein patterns and biological variables
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1559651/
https://www.ncbi.nlm.nih.gov/pubmed/16606449
http://dx.doi.org/10.1186/1471-2105-7-198
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