dc.contributor.author | Myrianthopoulos, V | |
dc.contributor.author | Gaboriaud-Kolar, N | |
dc.contributor.author | Tallant, C | |
dc.contributor.author | Hall, M-L | |
dc.contributor.author | Grigoriou, S | |
dc.contributor.author | Brownlee, PM | |
dc.contributor.author | Fedorov, O | |
dc.contributor.author | Rogers, C | |
dc.contributor.author | Heidenreich, D | |
dc.contributor.author | Wanior, M | |
dc.contributor.author | Drosos, N | |
dc.contributor.author | Mexia, N | |
dc.contributor.author | Savitsky, P | |
dc.contributor.author | Bagratuni, T | |
dc.contributor.author | Kastritis, E | |
dc.contributor.author | Terpos, E | |
dc.contributor.author | Filippakopoulos, P | |
dc.contributor.author | Müller, S | |
dc.contributor.author | Skaltsounis, A-L | |
dc.contributor.author | Downs, JA | |
dc.contributor.author | Knapp, S | |
dc.contributor.author | Mikros, E | |
dc.coverage.spatial | United States | |
dc.date.accessioned | 2022-08-24T12:02:31Z | |
dc.date.available | 2022-08-24T12:02:31Z | |
dc.date.issued | 2016-10-13 | |
dc.identifier.citation | Journal of Medicinal Chemistry, 2016, 59 (19), pp. 8787 - 8803 | |
dc.identifier.issn | 0022-2623 | |
dc.identifier.uri | https://repository.icr.ac.uk/handle/internal/5323 | |
dc.identifier.eissn | 1520-4804 | |
dc.identifier.eissn | 1520-4804 | |
dc.identifier.doi | 10.1021/acs.jmedchem.6b00355 | |
dc.description.abstract | Bromodomains (BRDs) are epigenetic interaction domains currently recognized as emerging drug targets for development of anticancer or anti-inflammatory agents. In this study, development of a selective ligand of the fifth BRD of polybromo protein-1 (PB1(5)) related to switch/sucrose nonfermenting (SWI/SNF) chromatin remodeling complexes is presented. A compound collection was evaluated by consensus virtual screening and a hit was identified. The biophysical study of protein-ligand interactions was performed using X-ray crystallography and isothermal titration calorimetry. Collective data supported the hypothesis that affinity improvement could be achieved by enhancing interactions of the complex with the solvent. The derived SAR along with free energy calculations and a consensus hydration analysis using WaterMap and SZmap algorithms guided rational design of a set of novel analogues. The most potent analogue demonstrated high affinity of 3.3 μM and an excellent selectivity profile, thus comprising a promising lead for the development of chemical probes targeting PB1(5). | |
dc.format | Print-Electronic | |
dc.format.extent | 8787 - 8803 | |
dc.language | eng | |
dc.language.iso | eng | |
dc.publisher | AMER CHEMICAL SOC | |
dc.relation.ispartof | Journal of Medicinal Chemistry | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.subject | Cell Line | |
dc.subject | Computer Simulation | |
dc.subject | Crystallography, X-Ray | |
dc.subject | DNA-Binding Proteins | |
dc.subject | Drug Design | |
dc.subject | Humans | |
dc.subject | Ligands | |
dc.subject | Models, Molecular | |
dc.subject | Nuclear Proteins | |
dc.subject | Protein Binding | |
dc.subject | Protein Domains | |
dc.subject | Small Molecule Libraries | |
dc.subject | Structure-Activity Relationship | |
dc.subject | Transcription Factors | |
dc.title | Discovery and Optimization of a Selective Ligand for the Switch/Sucrose Nonfermenting-Related Bromodomains of Polybromo Protein-1 by the Use of Virtual Screening and Hydration Analysis. | |
dc.type | Journal Article | |
dcterms.dateAccepted | 2016-10-13 | |
dc.date.updated | 2022-08-24T07:34:21Z | |
rioxxterms.version | VoR | |
rioxxterms.versionofrecord | 10.1021/acs.jmedchem.6b00355 | |
rioxxterms.licenseref.startdate | 2016-10-13 | |
rioxxterms.type | Journal Article/Review | |
pubs.author-url | https://www.ncbi.nlm.nih.gov/pubmed/27617704 | |
pubs.issue | 19 | |
pubs.organisational-group | /ICR | |
pubs.organisational-group | /ICR/Primary Group | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Cancer Biology | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Cancer Biology/Epigenetics and Genome Stability | |
pubs.publication-status | Published | |
pubs.volume | 59 | |
icr.researchteam | Genome Stability | |
dc.contributor.icrauthor | Downs, Jessica | |
icr.provenance | Deposited by Prof Jessica Downs on 2022-08-24. Deposit type is initial. No. of files: 1. Files: Discovery and Optimization of a Selective Ligand for the SwitchSucrose Nonfermenting-Related Bromodomains of Polybromo Prote.pdf | |