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Application of Celluspots peptide arrays for the analysis of the binding specificity of epigenetic reading domains to modified histone tails

BACKGROUND: Epigenetic reading domains are involved in the regulation of gene expression and chromatin state by interacting with histones in a post-translational modification specific manner. A detailed knowledge of the target modifications of reading domains, including enhancing and inhibiting seco...

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Autores principales: Bock, Ina, Kudithipudi, Srikanth, Tamas, Raluca, Kungulovski, Goran, Dhayalan, Arunkumar, Jeltsch, Albert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3176149/
https://www.ncbi.nlm.nih.gov/pubmed/21884582
http://dx.doi.org/10.1186/1471-2091-12-48
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author Bock, Ina
Kudithipudi, Srikanth
Tamas, Raluca
Kungulovski, Goran
Dhayalan, Arunkumar
Jeltsch, Albert
author_facet Bock, Ina
Kudithipudi, Srikanth
Tamas, Raluca
Kungulovski, Goran
Dhayalan, Arunkumar
Jeltsch, Albert
author_sort Bock, Ina
collection PubMed
description BACKGROUND: Epigenetic reading domains are involved in the regulation of gene expression and chromatin state by interacting with histones in a post-translational modification specific manner. A detailed knowledge of the target modifications of reading domains, including enhancing and inhibiting secondary modifications, will lead to a better understanding of the biological signaling processes mediated by reading domains. RESULTS: We describe the application of Celluspots peptide arrays which contain 384 histone peptides carrying 59 post translational modifications in different combinations as an inexpensive, reliable and fast method for initial screening for specific interactions of reading domains with modified histone peptides. To validate the method, we tested the binding specificities of seven known epigenetic reading domains on Celluspots peptide arrays, viz. the HP1ß and MPP8 Chromo domains, JMJD2A and 53BP1 Tudor domains, Dnmt3a PWWP domain, Rag2 PHD domain and BRD2 Bromo domain. In general, the binding results agreed with literature data with respect to the primary specificity of the reading domains, but in almost all cases we obtained additional new information concerning the influence of secondary modifications surrounding the target modification. CONCLUSIONS: We conclude that Celluspots peptide arrays are powerful screening tools for studying the specificity of putative reading domains binding to modified histone peptides.
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spelling pubmed-31761492011-09-20 Application of Celluspots peptide arrays for the analysis of the binding specificity of epigenetic reading domains to modified histone tails Bock, Ina Kudithipudi, Srikanth Tamas, Raluca Kungulovski, Goran Dhayalan, Arunkumar Jeltsch, Albert BMC Biochem Research Article BACKGROUND: Epigenetic reading domains are involved in the regulation of gene expression and chromatin state by interacting with histones in a post-translational modification specific manner. A detailed knowledge of the target modifications of reading domains, including enhancing and inhibiting secondary modifications, will lead to a better understanding of the biological signaling processes mediated by reading domains. RESULTS: We describe the application of Celluspots peptide arrays which contain 384 histone peptides carrying 59 post translational modifications in different combinations as an inexpensive, reliable and fast method for initial screening for specific interactions of reading domains with modified histone peptides. To validate the method, we tested the binding specificities of seven known epigenetic reading domains on Celluspots peptide arrays, viz. the HP1ß and MPP8 Chromo domains, JMJD2A and 53BP1 Tudor domains, Dnmt3a PWWP domain, Rag2 PHD domain and BRD2 Bromo domain. In general, the binding results agreed with literature data with respect to the primary specificity of the reading domains, but in almost all cases we obtained additional new information concerning the influence of secondary modifications surrounding the target modification. CONCLUSIONS: We conclude that Celluspots peptide arrays are powerful screening tools for studying the specificity of putative reading domains binding to modified histone peptides. BioMed Central 2011-08-31 /pmc/articles/PMC3176149/ /pubmed/21884582 http://dx.doi.org/10.1186/1471-2091-12-48 Text en Copyright ©2011 Bock 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 Research Article
Bock, Ina
Kudithipudi, Srikanth
Tamas, Raluca
Kungulovski, Goran
Dhayalan, Arunkumar
Jeltsch, Albert
Application of Celluspots peptide arrays for the analysis of the binding specificity of epigenetic reading domains to modified histone tails
title Application of Celluspots peptide arrays for the analysis of the binding specificity of epigenetic reading domains to modified histone tails
title_full Application of Celluspots peptide arrays for the analysis of the binding specificity of epigenetic reading domains to modified histone tails
title_fullStr Application of Celluspots peptide arrays for the analysis of the binding specificity of epigenetic reading domains to modified histone tails
title_full_unstemmed Application of Celluspots peptide arrays for the analysis of the binding specificity of epigenetic reading domains to modified histone tails
title_short Application of Celluspots peptide arrays for the analysis of the binding specificity of epigenetic reading domains to modified histone tails
title_sort application of celluspots peptide arrays for the analysis of the binding specificity of epigenetic reading domains to modified histone tails
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3176149/
https://www.ncbi.nlm.nih.gov/pubmed/21884582
http://dx.doi.org/10.1186/1471-2091-12-48
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