Cargando…
Methods for Activity Analysis of the Proteins that Regulate Histone Methylation
The enzymes that regulate histone methylation states and the protein domains that recognize methylated histone residues have been implicated in a number of human diseases, including cancer, as a result of their ability to affect transcriptional changes by altering chromatin structure. These proteins...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bentham Open
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3180180/ https://www.ncbi.nlm.nih.gov/pubmed/21966349 http://dx.doi.org/10.2174/1875397301005010095 |
_version_ | 1782212593366073344 |
---|---|
author | Quinn, Amy M Simeonov, Anton |
author_facet | Quinn, Amy M Simeonov, Anton |
author_sort | Quinn, Amy M |
collection | PubMed |
description | The enzymes that regulate histone methylation states and the protein domains that recognize methylated histone residues have been implicated in a number of human diseases, including cancer, as a result of their ability to affect transcriptional changes by altering chromatin structure. These proteins are recognized as potential therapeutic targets for the treatment of diseases associated with epigenetic disruption; however, few inhibitors of their activity have been identified. The majority of histone demethylase and methyltransferase enzyme inhibitors have been discovered on the basis of their structural similarity to substrates or known inhibitors of enzymes with analogous mechanisms. The general lack of potency and specificity of these compounds indicates that novel chemotypes are needed to address the large number of recently discovered histone-modifying enzymes. High-throughput screening (HTS) allows rapid testing of chemically diverse small molecule libraries, provided assays amenable to HTS exist. Here we review the biochemical and cellular assays available for testing the proteins and enzymes that regulate histone methylation. Progress in the development of high-throughput, sensitive, and robust assays will enable discovery of small molecules for epigenetic therapy. |
format | Online Article Text |
id | pubmed-3180180 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Bentham Open |
record_format | MEDLINE/PubMed |
spelling | pubmed-31801802011-09-30 Methods for Activity Analysis of the Proteins that Regulate Histone Methylation Quinn, Amy M Simeonov, Anton Curr Chem Genomics Article The enzymes that regulate histone methylation states and the protein domains that recognize methylated histone residues have been implicated in a number of human diseases, including cancer, as a result of their ability to affect transcriptional changes by altering chromatin structure. These proteins are recognized as potential therapeutic targets for the treatment of diseases associated with epigenetic disruption; however, few inhibitors of their activity have been identified. The majority of histone demethylase and methyltransferase enzyme inhibitors have been discovered on the basis of their structural similarity to substrates or known inhibitors of enzymes with analogous mechanisms. The general lack of potency and specificity of these compounds indicates that novel chemotypes are needed to address the large number of recently discovered histone-modifying enzymes. High-throughput screening (HTS) allows rapid testing of chemically diverse small molecule libraries, provided assays amenable to HTS exist. Here we review the biochemical and cellular assays available for testing the proteins and enzymes that regulate histone methylation. Progress in the development of high-throughput, sensitive, and robust assays will enable discovery of small molecules for epigenetic therapy. Bentham Open 2011-08-22 /pmc/articles/PMC3180180/ /pubmed/21966349 http://dx.doi.org/10.2174/1875397301005010095 Text en © Quinn and Simeonov; Licensee Bentham Open. http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited. |
spellingShingle | Article Quinn, Amy M Simeonov, Anton Methods for Activity Analysis of the Proteins that Regulate Histone Methylation |
title | Methods for Activity Analysis of the Proteins that Regulate Histone Methylation |
title_full | Methods for Activity Analysis of the Proteins that Regulate Histone Methylation |
title_fullStr | Methods for Activity Analysis of the Proteins that Regulate Histone Methylation |
title_full_unstemmed | Methods for Activity Analysis of the Proteins that Regulate Histone Methylation |
title_short | Methods for Activity Analysis of the Proteins that Regulate Histone Methylation |
title_sort | methods for activity analysis of the proteins that regulate histone methylation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3180180/ https://www.ncbi.nlm.nih.gov/pubmed/21966349 http://dx.doi.org/10.2174/1875397301005010095 |
work_keys_str_mv | AT quinnamym methodsforactivityanalysisoftheproteinsthatregulatehistonemethylation AT simeonovanton methodsforactivityanalysisoftheproteinsthatregulatehistonemethylation |