LAUSR

We rationally designed a series of amphiphilic hepta‐peptides enriched with a chemically conjugated guanidiniocarbonylpyrrole (GCP) unit at the lysine side chain. All peptides are composed of polar (GCP) and non‐polar (cyclohexyl alanine) residues but differ in their sequence periodicity, resulting in different secondary as well as supramolecular structures. CD spectra revealed the assembly of β‐sheet‐, α‐helical and random structures for peptides 1, 2 and 3, respectively. Consequently, this enabled the formation of distinct supramolecular assemblies such as fibres, nanorod‐like or spherical aggregates. Notably, all three cationic peptides are equipped with the anion‐binding GCP unit and thus possess a nucleic acid‐binding centre. However, only the helical (2) and the unstructured (3) peptide were able to assemble into small virus‐like DNA‐polyplexes and effectively deliver DNA into cells. Notably, as both peptides (2 and 3) were also capable of siRNA‐delivery, they could be utilized to downregulate expression of the caner‐relevant protein Survivin.