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Updated: May 17, 2026

Delivery of Therapeutic siRNA to the CNS Using Cationic and Anionic Liposomes
Published on: July 23, 2016
Histidine-rich cationic amphipathic peptides for plasmid DNA and siRNA delivery
Antoine Kichler1, A James Mason, Arnaud Marquette
1Laboratoire de Pharmacologie Chimique et Génétique et d'Imagerie, U1022 INSERM, Paris, France. antoine.kichler@parisdescartes.fr
Abstract:
Amphipathic, pH-responsive, membrane-active peptides such as LAH4 and derivatives thereof have the ability to effectively deliver genes and small interfering RNA (siRNA) into mammalian cells. Their ability to bind and protect nucleic acids and then disrupt membranes when activated at low pH enables them to harness the endocytic machinery to deliver cargo efficiently and with low associated toxicity. This chapter describes protocols for the chemical synthesis of transfection peptides of the LAH4 family, complex formation with nucleic acids, and their use for the in vitro delivery of either plasmid DNA or siRNA into mammalian cell lines.
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