Polypeptide-Folded Artificial Ferroprotein Promotes Ferroptosis in Multiple Tumor Cells.

Abstract

Although the current nanozymes, such as Fe3O4 nanoparticles, exhibit biocatalytic activities, they dramatically differ from natural enzymes, lacking a degradable organic framework and an intrinsically flexible structure. Single-chain folding of a synthetic polypeptide by metal coordination can mimic metalloproteins more similarly. A triblock PEG-polypeptide copolymer, poly(ethylene glycol)-b-poly(but-3-yn-1-yl glutamate)-b-poly(tert-butyl glutamate) [EG113-b-(Glu-yne)48-b-(Glu-tBu)61], was synthesized by NCA polymerization. The alkyne side groups on the central Glu-yne block were intramolecularly cross-linked by Fe3(CO)12 coordination. After thermolysis, the CO ligand was completely removed, yielding an artificial ferroprotein (AFP) with amorphous Fe/FeOx nanoclusters locked within the cross-linked region. While the parent triblock copolypeptide displayed negligible cytotoxicity on human normal cell lines (BEAS-2B and LO2), AFPs induced evident ferroptosis on four different cancer cell lines (PANC-1, HT1080, MCF-7, and A549) even with a low Fe content at 1.6 wt %.