Hydrogels, highly hydrated polymer networks, underpin both natural barriers such as mucus and numerous biomedical applications. Mucins, the glycoprotein constituents of mucus, achieve their viscoelasticity through peptide backbones enriched in proline, threonine, and serine interlaced with complex glycans. Mimicking this dual peptide-glycan architecture has proven difficult, yet essential for probing mucus functions in health and disease. Recent strategies have employed the α-helical coiled-coil scaffold hFF03 as a modular hydrogelator. Researchers in the Koksch Group at the Freie Universität Berlin, published in Peptide Science, systematically introduce histidine residues and monosaccharides into hFF03 to evaluate how glycosylation and divalent metal coordination shape peptide structure, rheology, and morphology.

The 26-residue hFF03 scaffold was diversified by substituting Lys at position 4, 25, or both with His, thereby creating accessible imidazole ligands for metal binding. In parallel, mannose or galactose was conjugated at Lys18 via a glutaric anhydride linker. The resulting library encompassed twelve (glyco)peptides, including His-free controls. Circular dichroism, CD, oscillatory rheology, and cryo-transmission electron microscopy, cryo-TEM, were employed to assess conformational and viscoelastic consequences of Cu²⁺, Zn²⁺, Fe²⁺, or Ca²⁺ addition under physiological pH and temperature.

CD analysis revealed that metal-free glycopeptides largely preserved higher-order structures characteristic of hFF03. However, incorporation of His introduced metal sensitivity. Position was decisive: His at residue 4 maintained robust higher-order structure but adopted more α-helical character upon Cu²⁺ addition. His at residue 25 yielded atypical CD signatures, including non-assignable spectra with Zn²⁺ or Ca²⁺, suggesting local distortion or C-terminal imidazole–carboxylate interactions. Double substitution, K4H/K25H, produced pH-sensitive peptides prone to precipitation above pH 7.4, yet demonstrated marked metal-dependent conformational switching. Glycan identity further modulated these behaviors, with galactose often favoring helical stabilization compared to mannose.

Viscoelastic profiling uncovered a delicate interplay between histidine placement, glycan identity, and metal coordination. His at position 4: hydrogels retained stiffness comparable to hFF03; mannosylation softened gels, while galactosylation stiffened them. Cu²⁺ generally reduced storage modulus, G′, though Cu²⁺/Gal combinations could increase rigidity. His at position 25: substitution alone markedly weakened hydrogels, ~80% reduction in G′. Yet, glycosylation reversed this trend: hFF-K25H-GA-Gal displayed the highest stiffness across the library, particularly with Cu²⁺, highlighting cooperative influence from glycan hydroxyl coordination. Double His substitution: despite expectations of cumulative coordination, K4H/K25H variants did not universally stiffen gels; effects were glycan- and metal-specific. Notably, glycosylated disubstituted peptides showed net stiffening upon metal addition, whereas aglycons softened.

Cryo-TEM underscored these rheological findings. hFF-K25H-GA-Gal formed long, slender fibrils in the absence of metal but collapsed into dense fiber bundles upon Cu²⁺ addition. Dark electron-dense spots along the bundles suggested localized Cu²⁺ clusters cross-linking individual fibrils, consistent with heightened viscoelasticity. By contrast, His4 variants displayed no morphological response to copper, affirming residue position as a key determinant.

Hydrogel mechanics can be tuned with remarkable sensitivity by triadic interplay among histidine location, glycan identity, and divalent metal ions. While His25 alone compromises gel strength, His25 coupled with galactose and Cu²⁺ yields the stiffest hydrogels, mimicking the responsiveness of native mucins to trace metal concentrations. These findings establish design rules for biomimetic glycopeptide hydrogels and highlight the potential of combining site-specific glycosylation with pH-switchable histidine coordination to engineer adaptive, stimulus-responsive materials.