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Updated: Jun 29, 2025

Using Lipid Nanoparticles for the Delivery of Chemically Modified mRNA into Mammalian Cells
Published on: June 10, 2022
N-terminal modification of an LAH4-derived peptide increases mRNA delivery in the presence of serum
Candice Dussouillez1,2, Morane Lointier3, Mohammed-Karim Sebane1,2
1Laboratoire de Conception et Application de Molécules Bioactives UMR7199 CNRS, Université de Strasbourg, 3BioTeam, Faculté de Pharmacie, Illkirch, France.
Abstract:
The recently developed mRNA-based coronavirus SARS-CoV-2 vaccines highlighted the great therapeutic potential of the mRNA technology. Although the lipid nanoparticles used for the delivery of the mRNA are very efficient, they showed, in some cases, the induction of side effects as well as the production of antibodies directed against particle components. Thus, the development of alternative delivery systems is of great interest in the pursuit of more effective mRNA treatments. In the present work, we evaluated the mRNA transfection capacities of a series of cationic histidine-rich amphipathic peptides derived from LAH4. We found that while the LAH4-A1 peptide was an efficient carrier for mRNA, its activity was highly serum sensitive. Interestingly, modification of this cell penetrating peptide at the N-terminus with two tyrosines or with salicylic acid allowed to confer serum resistance to the carrier.
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