Adv Mater. 2026 May 2:e18756. doi: 10.1002/adma.202518756. Online ahead of print.
ABSTRACT
Sequence-controlled polymers, such as polypeptides, offer a versatile platform for tuning the microenvironment of catalytic centers, drawing inspiration from enzymes while enabling a larger design space, structural flexibility, automated synthesis, and compatibility with closed-loop optimization. Here, we designed an artificial oxidase system by immobilizing Fe(III)-protoporphyrin IX onto a lysine residue in synthetic decapeptides via amide linkage. Using hydrogen peroxide as the oxidant and acetophenone as a model substrate, we used an active-learning-guided closed-loop workflow to prioritize peptide sequences across 233 variants over 20 rounds. Statistical analysis revealed that sulfur-containing residues-cysteine and methionine-consistently enhanced activity when positioned adjacent to the coordination site. Notably, although sequence optimization began from random inputs, the algorithm quickly converged on cysteine-containing motifs, consistent with features found in natural oxidases. Thioether-containing methionine was also found to promote catalysis, extending the relevance of sulfur-based coordination beyond naturally occurring systems. These findings demonstrate the application of data-driven sequence design for developing tunable, enzyme-inspired catalysts with simplified architectures.
PMID:42068197 | DOI:10.1002/adma.202518756
