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...

Descripción completa

Detalles Bibliográficos
Autores principales: Quinn, Amy M, Simeonov, Anton
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