A Potent Conformation-Constrained Synthetic Peptide Mimic of a Homeodomain Selectively Regulates Target Genes in Cells.
Basusree GhoshLiberalis Debraj BoilaSusobhan ChoudhuryPriya MondalSayan BhattacharjeeSamir Kumar PalAmitava SenguptaSiddhartha RoyPublished in: ACS chemical biology (2018)
DNA, as a target for therapeutic intervention, remains largely unexplored. DLX-4, a homeodomain containing transcription factor, and its spliced isoforms play crucial roles in many aspects of cellular biochemistry and important roles in many diseases. A smaller peptide mimicking the homeodomain of the transcription factor DLX-4 was designed and synthesized by suitable conjoining of its modified DNA-binding elements. The peptide binds to DLX-4 target sites on the regulatory region of the globin gene cluster with native-like affinity and specificity in vitro. When conjugated to cell penetrating and nuclear localization sequences, it upregulated some of the genes repressed by DLX-4 or its isoforms, such as β- and γ-globin genes in erythropoietin-induced differentiating CD34+ human hematopoietic stem/progenitor cells with high specificity by competing with the respective binding sites. Engineered peptides mimicking DNA-binding domains of transcription factors offer the potential for creating synthetic molecules for directly targeting DNA sites with high specificity.
Keyphrases
- transcription factor
- dna binding
- genome wide identification
- genome wide
- circulating tumor
- endothelial cells
- randomized controlled trial
- induced apoptosis
- single molecule
- bioinformatics analysis
- cell free
- structural basis
- cell therapy
- diabetic rats
- high glucose
- cell cycle arrest
- mesenchymal stem cells
- photodynamic therapy
- computed tomography
- stem cells
- copy number
- genome wide analysis
- induced pluripotent stem cells
- drug induced
- risk assessment
- oxidative stress
- cell proliferation
- contrast enhanced
- genetic diversity
- pluripotent stem cells