Bifunctional Peptide that Anneals to Damaged Collagen and Clusters TGF-β Receptors Enhances Wound Healing.
Sayani ChattopadhyayLeandro B C TeixeiraLaura L KiesslingJonathan F McAnultyRonald T RainesPublished in: ACS chemical biology (2022)
Transforming growth factor-β (TGF-β) plays important roles in wound healing. The activity of TGF-β is initiated upon the binding of the growth factor to the extracellular domains of its receptors. We sought to facilitate the activation by clustering these extracellular domains. To do so, we used a known peptide that binds to TGF-β receptors without diminishing their affinity for TGF-β. We conjugated this peptide to a collagen-mimetic peptide that can anneal to the damaged collagen in a wound bed. We find that the conjugate enhances collagen deposition and wound closure in mice in a manner consistent with the clustering of TGF-β receptors. This strategy provides a means to upregulate the TGF-β signaling pathway without adding exogenous TGF-β and could inspire means to treat severe wounds.
Keyphrases
- transforming growth factor
- wound healing
- epithelial mesenchymal transition
- growth factor
- signaling pathway
- type diabetes
- single cell
- oxidative stress
- photodynamic therapy
- drug delivery
- tissue engineering
- cell proliferation
- rna seq
- cancer therapy
- endoplasmic reticulum stress
- transcription factor
- dna binding
- binding protein
- surgical site infection