Efficient Inhibition of TGF-β Signaling via Cytosolic Delivery of a Smad2/3-Binding Peptide Using the Cell-Penetrating PG-Surfactant DKDKC 12 -K 5 to Block Smad2/3 Nuclear Translocation

High Resolution Image Download MS PowerPoint Slide Targeting intracellular signaling molecules that translocate to the nucleus is a promising approach for peptide-based therapeutics. Here, we focused on Smad2/3, key mediators of TGF-β signaling that act as transcription factors upon nuclear entry. To inhibit their nuclear localization, we delivered an Smad2/3-binding SARA peptide into the cytoplasm using our previously developed cell-penetrating carrier, cpPG. A conjugate, SARA-cpPG, was synthesized by linking the SARA peptide to Mal-DKDKC 12 -K 5, a cpPG derivative with an N-terminal maleimide. In A549 cells, SARA-cpPG showed uptake over 20-fold higher than that of the SARA peptide alone and retained cytoplasmic localization. Functionally, SARA-cpPG suppressed TGF-β1-induced actin polymerization and cell migration, comparable to the effects of receptor kinase inhibitor LY2157299. These effects were not observed with cpPG alone or a control conjugate (SARAm-cpPG) containing a nonbinding mutant peptide. Mechanistic studies revealed that SARA-cpPG did not inhibit Smad2/3 phosphorylation but reduced TGF-β target gene expression, suggesting a blockade of nuclear translocation. This suppression was absent in treatments with SARAm-cpPG, cpPG alone, or a non-cytoplasm-specific carrier conjugate (SARA-R8). These findings demonstrate that cpPG enables efficient cytosolic delivery of functional peptides and supports a strategy for intracellular peptide therapeutics targeting nuclear signaling pathways.