4.7 Article

Arginine-Rich Polymers with Pore-Forming Capability Enable Efficient Intracellular Delivery via Direct Translocation Across Cell Membrane

Journal

ADVANCED HEALTHCARE MATERIALS
Volume 11, Issue 14, Pages -

Publisher

WILEY
DOI: 10.1002/adhm.202200371

Keywords

arginine-rich polymers; cell penetration; direct transloction; endocytosis-independent pathways; gene delivery

Funding

  1. National Key Research and Development Programs of China [2018YFA0209700]
  2. National Natural Science Foundation of China (NSFC) [22077073]
  3. Frontiers Science Center for New Organic Matter, Nankai University [63181206]
  4. Fundamental Research Funds for the Central Universities, Nankai University [63206015]

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A series of arginine-rich cell penetrating polymers are designed and synthesized to efficiently deliver biomacromolecules or drugs across the cell membrane by inducing pore formation on the cell membrane, thus avoiding endosomal entrapment. PTn-R2-C6, a polymer with two arginine residues and a flexible hexanoic acid linker in each side chain, shows excellent pore-forming ability and achieves higher transfection efficiency and lower cytotoxicity compared to the gold-standard transfection reagent PEI 25K. These findings suggest that PTn-R2-C6 has great potential as a safe and efficient gene transfection reagent for various applications including disease treatments, vaccine development, and biomedical research.
Efficient delivery of biomacromolecules or drugs across the cell membrane via endocytosis usually encounters inevitable entrapment in endosomes and subsequent degradation in lyso-endosomes. To address this issue, a series of arginine-rich cell penetrating polymers is designed and synthesized, which internalize into cells by inducing the formation of pores on the cell membrane, thereby crossing the cell membrane via direct translocation that fundamentally avoids endo/lysosomal entrapment. The structure-activity relationship studies show that PTn-R2-C6, which is a type of polymer that has two arginine residues and a flexible hexanoic acid linker in each side chain, exhibits excellent pore-formation ability on the cell membrane. Further investigations indicate that PTn-R2-C6 rapidly transports plasmid DNAs into cytosol through a similar endocytosis-independent pathway, thereby achieving significantly higher transfection efficiency and lower cytotoxicity than the gold-standard transfection reagent PEI 25K. These results suggest the great potential of PTn-R2-C6 as a safe and efficient gene transfection reagent for wide applications including disease treatments, vaccine development, and biomedical research purposes.

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