Evaluation of linker length effects on a BET bromodomain probe.

Fueled by the therapeutic potential of the epigenetic machinery, BET bromodomains have seen high interest as drug targets. Herein, we introduce different linkers to a BET bromodomain benzodiazepine ligand (I-BET762) to gauge its implications in the development of hybrid drugs, imaging probes and small molecule drug conjugates. Biophysical studies confirmed minimal disruption to binding of the BRD4 cavity by the synthesized entities, which includes imaging probes. Target engagement was confirmed in a cellular context, but poor membrane diffusion was found despite efficient localization in the nuclei after membrane disruption. Our study highlights challenges and opportunities for the successful design of benzodiazepine-derived drug-delivery systems.

Keywords

Benzodiazepines, Cell Line, Tumor, Cell Nucleus, Drug Design, Fluoresceins, Fluorescent Dyes, Humans, Ligands, Molecular Structure, Nuclear Proteins, Protein Domains

Journal Title

Chemical Communications

Journal ISSN

1359-7345
1364-548X

Volume Title

55

Publisher

Royal Society of Chemistry

Publisher DOI

https://doi.org/10.1039/c9cc05054j

Rights and licensing

Sponsorship

Royal Society (URF\R\180019)

We thank the Hovione Farmaciência (PhD studentship to R. T.) Royal Society (URF\R\180019 to G. J. L. B.), DFG (SI 2117/1-1 to F. S.), FCT Portugal (IF/00624/2015 to G. J. L. B., CEECIND/04518/2017 to P. M. S. D. C. and CEECIND/00887/2017 to T. R., and 02/SAICT/2017, Grant 28333 to T. R.) and the Medical Research Council (MRC grant MR/N010051/1 to P. F.) for funding.

Collections

University of Cambridge Research Outputs (Articles and Conferences)