Wydział Chemii

Jakub Gawłowski

Mariusz Dziadas

Aleksandra Mikołajczyk-Tarnawa

Arian Kola

Daniela Valensin

Agnieszka Matera-Witkiewicz

Magdalena Rowińska-Żyrek

2026

Inorganic Chemistry

65

15845-15854

10.1021/acs.inorgchem.6c02172

Naukowa

Angielski

Artykuł

We redesign the histidine-rich antimicrobial peptide clavanin C through stereochemical inversion to generate proteolytically stable metallopeptidomimetics while preserving metal-binding functionality and antimicrobial activity. Two analogues were prepared: an all-d amino acid peptide and a retro-inverso variant. Remarkably, despite complete sequence reversal and inversion of chirality, both mimetics retain Cu²⁺ coordination through the N-terminal ATCUN motif, forming characteristic square-planar 4N complexes. Zn²⁺ binding is likewise preserved and involves a cluster of histidine residues located on one face of the amphipathic α-helix. This distinction reveals two complementary design principles: sequence-encoded metal binding in the case of Cu²⁺ versus topology-driven coordination for Zn²⁺. Both stereochemical designs dramatically increase resistance to proteolytic degradation while maintaining the helical fold under membrane-mimicking conditions. In antimicrobial assays, the retro-inverso analogue and its metal complexes display particularly strong activity against methicillin-resistant Staphylococcus aureus (MRSA), with minimum inhibitory concentrations as low as 8 μg/mL and no detectable cytotoxicity toward mammalian cells. Taken together, our data show that both d-amino acid substitution and retro-inverso design can stabilize clavanin C while retaining its metal-binding ability and antimicrobial activity, providing a general strategy for the development of proteolytically stable antimicrobial metallopeptidomimetics.

Antimicrobial activity, Bacteria, Metals, Monomers, Peptides and proteins

CC-BY

http://dx.doi.org/10.1021/acs.inorgchem.6c02172

https://www.acs.org/content/acs/en.html