Extended Data Fig. 1: Headgroup-modified lipids for IL-12 conjugation. | Nature Materials

Extended Data Fig. 1: Headgroup-modified lipids for IL-12 conjugation.

From: IL-12-releasing nanoparticles for effective immunotherapy of metastatic ovarian cancer

Extended Data Fig. 1: Headgroup-modified lipids for IL-12 conjugation.

a, Chemical structure of headgroup-modified lipids with either chelated nickel or N-aryl maleimide. N-aryl maleimide was employed to prevent potential thiosuccinimide retro-Michael addition and subsequent thiol-exchange, as this headgroup favors thiosuccinimide hydrolysis into stable succinamic acid thioethers. b, IL-12 crystal structure derived from PDB 1F45 showing C-terminus used to engineered terminal poly-histidine (polyHis) tag and terminal cysteine. c, Reaction pathway for irreversible maleimide-based conjugation with thiols.

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