Progress in the development and application of small molecule inhibitors of bromodomain-acetyl-lysine interactions.

Bromodomains, protein modules that recognize and bind to acetylated lysine, are emerging as important components of cellular machinery. These acetyl-lysine (KAc) "reader" domains are part of the write-read-erase concept that has been linked with the transfer of epigenetic information. By r...

全面介绍

书目详细资料
Main Authors: Hewings, D, Rooney, T, Jennings, L, Hay, D, Schofield, C, Brennan, P, Knapp, S, Conway, S
格式: Journal article
语言:English
出版: 2012
_version_ 1826281429917499392
author Hewings, D
Rooney, T
Jennings, L
Hay, D
Schofield, C
Brennan, P
Knapp, S
Conway, S
author_facet Hewings, D
Rooney, T
Jennings, L
Hay, D
Schofield, C
Brennan, P
Knapp, S
Conway, S
author_sort Hewings, D
collection OXFORD
description Bromodomains, protein modules that recognize and bind to acetylated lysine, are emerging as important components of cellular machinery. These acetyl-lysine (KAc) "reader" domains are part of the write-read-erase concept that has been linked with the transfer of epigenetic information. By reading KAc marks on histones, bromodomains mediate protein-protein interactions between a diverse array of partners. There has been intense activity in developing potent and selective small molecule probes that disrupt the interaction between a given bromodomain and KAc. Rapid success has been achieved with the BET family of bromodomains, and a number of potent and selective probes have been reported. These compounds have enabled linking of the BET bromodomains with diseases, including cancer and inflammation, suggesting that bromodomains are druggable targets. Herein, we review the biology of the bromodomains and discuss the SAR for the existing small molecule probes. The biology that has been enabled by these compounds is summarized.
first_indexed 2024-03-07T00:28:40Z
format Journal article
id oxford-uuid:7f054681-270a-4838-b674-c656370fa6cf
institution University of Oxford
language English
last_indexed 2024-03-07T00:28:40Z
publishDate 2012
record_format dspace
spelling oxford-uuid:7f054681-270a-4838-b674-c656370fa6cf2022-03-26T21:14:04ZProgress in the development and application of small molecule inhibitors of bromodomain-acetyl-lysine interactions.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:7f054681-270a-4838-b674-c656370fa6cfEnglishSymplectic Elements at Oxford2012Hewings, DRooney, TJennings, LHay, DSchofield, CBrennan, PKnapp, SConway, SBromodomains, protein modules that recognize and bind to acetylated lysine, are emerging as important components of cellular machinery. These acetyl-lysine (KAc) "reader" domains are part of the write-read-erase concept that has been linked with the transfer of epigenetic information. By reading KAc marks on histones, bromodomains mediate protein-protein interactions between a diverse array of partners. There has been intense activity in developing potent and selective small molecule probes that disrupt the interaction between a given bromodomain and KAc. Rapid success has been achieved with the BET family of bromodomains, and a number of potent and selective probes have been reported. These compounds have enabled linking of the BET bromodomains with diseases, including cancer and inflammation, suggesting that bromodomains are druggable targets. Herein, we review the biology of the bromodomains and discuss the SAR for the existing small molecule probes. The biology that has been enabled by these compounds is summarized.
spellingShingle Hewings, D
Rooney, T
Jennings, L
Hay, D
Schofield, C
Brennan, P
Knapp, S
Conway, S
Progress in the development and application of small molecule inhibitors of bromodomain-acetyl-lysine interactions.
title Progress in the development and application of small molecule inhibitors of bromodomain-acetyl-lysine interactions.
title_full Progress in the development and application of small molecule inhibitors of bromodomain-acetyl-lysine interactions.
title_fullStr Progress in the development and application of small molecule inhibitors of bromodomain-acetyl-lysine interactions.
title_full_unstemmed Progress in the development and application of small molecule inhibitors of bromodomain-acetyl-lysine interactions.
title_short Progress in the development and application of small molecule inhibitors of bromodomain-acetyl-lysine interactions.
title_sort progress in the development and application of small molecule inhibitors of bromodomain acetyl lysine interactions
work_keys_str_mv AT hewingsd progressinthedevelopmentandapplicationofsmallmoleculeinhibitorsofbromodomainacetyllysineinteractions
AT rooneyt progressinthedevelopmentandapplicationofsmallmoleculeinhibitorsofbromodomainacetyllysineinteractions
AT jenningsl progressinthedevelopmentandapplicationofsmallmoleculeinhibitorsofbromodomainacetyllysineinteractions
AT hayd progressinthedevelopmentandapplicationofsmallmoleculeinhibitorsofbromodomainacetyllysineinteractions
AT schofieldc progressinthedevelopmentandapplicationofsmallmoleculeinhibitorsofbromodomainacetyllysineinteractions
AT brennanp progressinthedevelopmentandapplicationofsmallmoleculeinhibitorsofbromodomainacetyllysineinteractions
AT knapps progressinthedevelopmentandapplicationofsmallmoleculeinhibitorsofbromodomainacetyllysineinteractions
AT conways progressinthedevelopmentandapplicationofsmallmoleculeinhibitorsofbromodomainacetyllysineinteractions