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bioRxiv · 10.1101/2024.01.20.576479

Bioreversible anionic cloaking enables intracellular protein delivery with ionizable lipid nanoparticles

Alamgir, A.·Ghosal, S.·DeLisa, M.·Alabi, C. A.
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Abstract

Protein-based therapeutics comprise a rapidly growing subset of pharmaceuticals, but enabling their delivery into cells for intracellular applications has been a longstanding challenge. To overcome the delivery barrier, we explored a reversible, bioconjugation-based approach to modify the surface charge of protein cargos with an anionic "cloak" to facilitate electrostatic complexation and delivery with lipid nanoparticle (LNP) formulations. We demonstrate that the conjugation of lysine-reactive sulfonated compounds can allow for the delivery of various protein cargos using FDA-approved LNP formulations of the ionizable cationic lipid DLin-MC3-DMA (MC3). We apply this strategy to functionally deliver RNase A for cancer cell killing as well as a full-length antibody to inhibit oncogenic {beta}-catenin signaling. Further, we show that LNPs encapsulating cloaked fluorescent proteins distribute to major organs in mice following systemic administration. Overall, our results point towards a generalizable platform that can be employed for intracellular delivery of a wide range of protein cargos.

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Alamgir, A., Ghosal, S., DeLisa, M., Alabi, C. A.. 2024-01-23. Bioreversible anionic cloaking enables intracellular protein delivery with ionizable lipid nanoparticles. https://doi.org/10.1101/2024.01.20.576479

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