In silico design and bioevaluation of selective benzotriazepine BRD4 inhibitors with potent antiosteoclastogenic activity.
Vishwa DeepakBinglin WangDwayne KootAbe KasongaXiao Xing StanderMagdalena CoetzeeBarend Andre StanderPublished in: Chemical biology & drug design (2017)
The bromodomain (BRD) and extra-terminal domain (BET) protein family bind to acetylated histones on lysine residues and act as epigenetic readers. Recently, the role of this protein family in bone loss has been gaining attention. Earlier studies have reported that benzotriazepine (Bzt) derivatives could be effective inhibitors of BET proteins. In this study, using in silico tools we designed three Bzt analogs (W49, W51, and W52). By docking, molecular simulations, and chemiluminescent Alpha Screen binding assay, we show that the studied analogs were selective at inhibiting BRD4 when compared to BRD2. Furthermore, we tested the effectiveness of these analogs on osteoclast formation and function. Among the examined analogs, Bzt-W49 and Bzt-W52 were found to be the most potent inhibitors of osteoclastogenesis without cytotoxicity in murine RAW264.7 osteoclast progenitors. Both the compounds also inhibited osteoclast formation without affecting cell viability in human CD14+ monocytes. Moreover, owing to attenuated osteoclastogenesis, actin ring formation and bone resorptive function of osteoclasts were severely perturbed. In conclusion, these results suggest that the novel BRD4-selective Bzt analogs designed in this study could be explored further for developing therapeutics against bone loss diseases characterized by excessive osteoclast activity.
Keyphrases
- bone loss
- molecular docking
- molecular dynamics simulations
- protein protein
- molecular dynamics
- endothelial cells
- small molecule
- high throughput
- randomized controlled trial
- binding protein
- systematic review
- gene expression
- amino acid
- dna methylation
- signaling pathway
- immune response
- single molecule
- transcription factor
- cell migration
- postmenopausal women
- bone mineral density