Nature Communications (Oct 2024)

Structuring lipid nanoparticles, DNA, and protein corona into stealth bionanoarchitectures for in vivo gene delivery

  • Serena Renzi,
  • Luca Digiacomo,
  • Daniela Pozzi,
  • Erica Quagliarini,
  • Elisabetta Vulpis,
  • Maria Valeria Giuli,
  • Angelica Mancusi,
  • Bianca Natiello,
  • Maria Gemma Pignataro,
  • Gianluca Canettieri,
  • Laura Di Magno,
  • Luca Pesce,
  • Valentina De Lorenzi,
  • Samuele Ghignoli,
  • Luisa Loconte,
  • Carmela Maria Montone,
  • Anna Laura Capriotti,
  • Aldo Laganà,
  • Carmine Nicoletti,
  • Heinz Amenitsch,
  • Marco Rossi,
  • Francesco Mura,
  • Giacomo Parisi,
  • Francesco Cardarelli,
  • Alessandra Zingoni,
  • Saula Checquolo,
  • Giulio Caracciolo

DOI
https://doi.org/10.1038/s41467-024-53569-8
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 20

Abstract

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Abstract Lipid nanoparticles (LNPs) play a crucial role in addressing genetic disorders, and cancer, and combating pandemics such as COVID-19 and its variants. Yet, the ability of LNPs to effectively encapsulate large-size DNA molecules remains elusive. This is a significant limitation, as the successful delivery of large-size DNA holds immense potential for gene therapy. To address this gap, the present study focuses on the design of PEGylated LNPs, incorporating large-sized DNA, departing from traditional RNA and ionizable lipids. The resultant LNPs demonstrate a unique particle morphology. These particles were further engineered with a DNA coating and plasma proteins. This multicomponent bionanoconstruct exhibits enhanced transfection efficiency and safety in controlled laboratory settings and improved immune system evasion in in vivo tests. These findings provide valuable insights for the design and development of bionanoarchitectures for large-size DNA delivery, opening new avenues for transformative gene therapies.