Efficient gene delivery into cells by a surprisingly small three-armed peptide ligand

Abstract

The development of new non-viral transfection vectors for gene transport into cells is of current interest. A small, three-armed peptide ligand 1 is derived from the cationic dipeptide Lys-Phe with an additional anion recognition site at its N-terminus, binds to DNA with high affinity (K ca. 10⁷ M⁻¹) and efficiently delivers a GFP plasmid into cells. Compared to the cationic polymer polyethyleneimine (PEI), routinely used as a standard vector for transfection, 1 is significantly more efficient and also less cytotoxic. As DLS and AFM studies show, ligand 1 condenses DNA into tightly packed cationic aggregates which are then taken up by the cells. In contrast, the analogous divalent peptide ligand 2 of identical amino acid sequence and the highly charged divalent DNA-binder 3 (Lys-Lys-Arg) do not enable gene delivery though they also bind with high affinity (2: K ca. 10⁶ M⁻¹; 3: K ca. 10⁷ M⁻¹). All three ligands are able to transfer genetic material into cells but only the trivalent gene carrier is able to escape from the endosome due to its superior buffering capacity.